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<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="other" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Morphology</journal-id><journal-title-group><journal-title xml:lang="en">Morphology</journal-title><trans-title-group xml:lang="ru"><trans-title>Морфология</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1026-3543</issn><issn publication-format="electronic">2949-2556</issn><publisher><publisher-name xml:lang="en">Eco-Vector</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">702031</article-id><article-id pub-id-type="doi">10.17816/morph.702031</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>Reviews</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>Научные обзоры</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">ENDOTHELIUM: MOLECULAR-GENETIC ORGANIZATION OF HISTOGENESIS AND SYSTEMATIC POSITION</article-title><trans-title-group xml:lang="ru"><trans-title>ЭНДОТЕЛИЙ: МОЛЕКУЛЯРНО-ГЕНЕТИЧЕСКАЯ ОРГАНИЗАЦИЯ ГИСТОГЕНЕЗА И СИСТЕМАТИЧЕСКОЕ ПОЛОЖЕНИЕ</trans-title></trans-title-group><trans-title-group xml:lang="zh"><trans-title/></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-8389-3841</contrib-id><contrib-id contrib-id-type="scopus">58898845100</contrib-id><contrib-id contrib-id-type="spin">2957-1687</contrib-id><name-alternatives><name xml:lang="en"><surname>Deev</surname><given-names>Roman</given-names></name><name xml:lang="ru"><surname>Деев</surname><given-names>Роман Вадимович</given-names></name><name xml:lang="zh"><surname></surname><given-names></given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>MD, Dr. Sci. (Medicine), Associate ProfessorFirst Deputy Director of the A.P. Avtsyn Research Institute of Human Morphology</p></bio><bio xml:lang="ru"><p>Кандидат медицинских наук, доцентПервый заместитель директора НИИ Морфологии человека имени академика А.П. Авцына</p></bio><email>romdey@gmail.com</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-2732-5676</contrib-id><contrib-id contrib-id-type="spin">1852-6469</contrib-id><name-alternatives><name xml:lang="en"><surname>Gladyshev</surname><given-names>Nikita</given-names></name><name xml:lang="ru"><surname>Гладышев</surname><given-names>Никита Сергеевич</given-names></name><name xml:lang="zh"><surname></surname><given-names></given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="ru"><p>Научный сотрудник</p></bio><email>krinege@mail.ru</email><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0009-0003-2251-0896</contrib-id><contrib-id contrib-id-type="spin">9815-0045</contrib-id><name-alternatives><name xml:lang="en"><surname>Zolkin</surname><given-names>Alexey</given-names></name><name xml:lang="ru"><surname>Золкин</surname><given-names>Алексей Геннадьевич</given-names></name><name xml:lang="zh"><surname></surname><given-names></given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="ru"><p>Научный сотрудник</p></bio><email>zolkin.ag@phystech.edu</email><xref ref-type="aff" rid="aff2"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Petrovsky National Research Centre of Surgery</institution></aff><aff><institution xml:lang="kk"></institution></aff><aff><institution xml:lang="pt"></institution></aff><aff><institution xml:lang="ru">Российский научный центр хирургии имени академика Б.В. Петровского</institution></aff><aff><institution xml:lang="zh"></institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">B.V. Petrovsky Russian Scientific Center of Surgery</institution></aff><aff><institution xml:lang="ru">Российский научный центр хирургии им. акад. Б.В. Петровского</institution></aff><aff><institution xml:lang="zh"></institution></aff></aff-alternatives><pub-date date-type="preprint" iso-8601-date="2026-06-04" publication-format="electronic"><day>04</day><month>06</month><year>2026</year></pub-date><volume>164</volume><issue>3</issue><issue-title xml:lang="ru"/><history><date date-type="received" iso-8601-date="2026-02-01"><day>01</day><month>02</month><year>2026</year></date><date date-type="accepted" iso-8601-date="2026-02-21"><day>21</day><month>02</month><year>2026</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; , Eco-Vector</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; , Эко-Вектор</copyright-statement><copyright-holder xml:lang="en">Eco-Vector</copyright-holder><copyright-holder xml:lang="ru">Эко-Вектор</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/" start_date="2029-06-04"/><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://eco-vector.com/for_authors.php#07</ali:license_ref></license></permissions><self-uri xlink:href="https://j-morphology.com/1026-3543/article/view/702031">https://j-morphology.com/1026-3543/article/view/702031</self-uri><abstract xml:lang="en"><p/><title>Introduction. Endothelial cells, which form the lining of blood vessels, lymphatic vessels, and cardiac chambers, are located within the body's internal environment, yet do not delimit it from the external environment. They have an epitheliomorphic organization and, therefore, are often considered representatives of the epithelial tissue system.</title> <title>Aim. To update modern data on the molecular-genetic and morpho-functional organization, reactivity and regeneration of the endothelium, which influence the understanding of its systematic affiliation.</title> <title>Results. The accumulated evidence indicates that, based on the combined data on the molecular signature of differentiation occurring during histogenesis, cytoskeletal proteins (vimentin), intercellular adhesion (CD31, CD34), intercellular signaling, products of specialized synthesis (von Willebrand coagulation factor), reactivity, and regeneration characteristics, endothelial cells correspond to tissues of the internal environment. Data on the functioning of transcription factors and their activity inducers, which are specific to epithelia and endothelium, are presented. Information on postnatal physiological and reparative regeneration, the presence of dispersed cambium, including that extending beyond the cell layer (bone marrow), further support this conclusion.</title> <title>Conclusion. Thus, in modern interpretations of physiological and reparative histogenesis of the endothelium, as well as in educational processes, the histological phenomena associated with it should be interpreted taking into account the general patterns characteristic of tissues of the internal environment.</title></abstract><trans-abstract xml:lang="ru"><p><bold>Введение.</bold> Эндотелиальные клетки, формирующие выстилку кровеносных, лимфатических сосудов и камер сердца расположены в составе внутренней среды организма, при этом не отграничивают ее от среды внешней, имеют эпителиоморфную организацию и в связи с последним нередко относятся к представителям системы эпителиальных тканей.</p> <p><bold>Цель обзора.</bold> Актуализировать современные данные о молекулярно-генетической и морфо-функциональной организации, реактивности и регенерации эндотелия, влияющих на понимание его систематической принадлежности.</p> <p><bold>Результаты.</bold> Накопленный фактический материал свидетельствует, что по совокупности данных о молекулярной сигнатуре дифференцировки, реализующейся в гистогенезе, белков цитоскелета (виментин), межклеточной адгезии (CD31, CD34 и др.), межклеточного сигналинга, продуктов специализированного синтеза (фактор свертывания фон Виллебранда), реактивности и особенностях регенерации, эндотелиоциты соответствуют представителям тканей внутренней среды. Представлены данные о функционировании различных для эпителиев и эндотелия транскрипционных факторов и индукторов их активности. Сведения о постанатальной физиологической и репаративной регенерации, наличие рассредоточенного камбия, в том числе вынесенного за пределы клеточного пласта (костный мозг) дополнительно подтверждают это суждение.</p> <p><bold>Заключение.</bold> Таким образом, при современной трактовке физиологического и репаративного гистогенеза эндотелия, а также в учебном процессе следует трактовать гистологические феномены, связанные с ним, с учетом общих закономерностей, характерных для тканей внутренней среды.</p></trans-abstract><trans-abstract xml:lang="zh"><p/></trans-abstract><kwd-group xml:lang="en"><kwd>Endothelium</kwd><kwd>endotheliocyte</kwd><kwd>angiogenesis</kwd><kwd>vasculogenesis</kwd><kwd>differentiation</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>Эндотелий</kwd><kwd>эндотелиоцит</kwd><kwd>ангиогенез</kwd><kwd>васкулогенез</kwd><kwd>дифференцировка</kwd></kwd-group><funding-group/></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><citation-alternatives><mixed-citation xml:lang="en">1.	Histology, Embryology, Cytology: a textbook / Yu. I. Afanasyev, B. V. Aleshin, N. P. Barsukov, et al.; edited by Yu. I. Afanasyev, N. A. Yurina. - 7th ed., revised and enlarged. - Moscow: GEOTAR-Media, 2024. - 832 p. - ISBN 978-5-9704-8785-3.</mixed-citation><mixed-citation xml:lang="ru">1.	Гистология, эмбриология, цитология : учебник / Ю. И. Афанасьев, Б. В. Алешин, Н. П. Барсуков и др.; под ред. Ю. И. Афанасьева, Н. А. Юриной. - 7-е изд. , перераб. и доп. - Москва : ГЭОТАР-Медиа, 2024. - 832 с. - ISBN 978-5-9704-8785-3.</mixed-citation></citation-alternatives></ref><ref id="B2"><label>2.</label><citation-alternatives><mixed-citation xml:lang="en">2.	Handbook of Histology: a textbook for students of medical universities and faculties, postgraduate students, and students of continuing medical education: in 2 volumes / edited by R. K. Danilov. Volume 1. - St. Petersburg: SpetsLit, 2011-, 2011. - 830. ISBN 978-5-299-00421-2.</mixed-citation><mixed-citation xml:lang="ru">2.	Руководство по гистологии : учебное пособие для студентов медицинских вузов и факультетов, аспирантов и слушателей системы дополнительного медицинского образования : в 2 т. / под ред. Р. К. Данилова. Т. 1. — Санкт-Петербург : СпецЛит, 2011-, 2011. — 830. ISBN 978-5-299-00421-2.</mixed-citation></citation-alternatives></ref><ref id="B3"><label>3.</label><citation-alternatives><mixed-citation xml:lang="en">3.	Connective tissue (histophysiology and biochemistry) / N. P. Omelyanenko, L. I. Slutsky; edited by S. P. Mironov; Federal State Institution "N. N. Priorov Central Institute of Traumatology and Orthopedics of the Russian Medical Technologies". - Moscow: Izvestia, 2009. ISBN 978-5-206-00740-4</mixed-citation><mixed-citation xml:lang="ru">3.	Соединительная ткань (гистофизиология и биохимия) / Н. П. Омельяненко, Л. И. Слуцкий ; под ред. С. П. Миронова ; Федеральное гос. учреждение "Центральный ин-т травматологии и ортопедии им. Н. Н. Приорова Росмедтехнологий". - Москва : Известия, 2009. ISBN 978-5-206-00740-4</mixed-citation></citation-alternatives></ref><ref id="B4"><label>4.</label><citation-alternatives><mixed-citation xml:lang="en">4.	Web resource https://humancelltreemap.mis.mpg.de/ accompanied by paper: Hatton IA, Galbraith ED, Merleau NSC, Miettinen TP, Smith BM, Shander JA. The human cell count and size distribution. Proc Natl Acad Sci U S A. 2023;120(39):e2303077120. doi:10.1073/pnas.2303077120</mixed-citation><mixed-citation xml:lang="ru">4. Web resource https://humancelltreemap.mis.mpg.de/ accompanied by paper: Hatton IA, Galbraith ED, Merleau NSC, Miettinen TP, Smith BM, Shander JA. The human cell count and size distribution. Proc Natl Acad Sci U S A. 2023;120(39):e2303077120. doi:10.1073/pnas.2303077120</mixed-citation></citation-alternatives></ref><ref id="B5"><label>5.</label><citation-alternatives><mixed-citation xml:lang="en">5.	Gansburgskii AN, Pavlov AV Endothelium. In the book: Handbook of Histology: a textbook for students of medical universities and faculties, postgraduate students and students of continuing medical education: in 2 volumes / edited by R. K. Danilov. Volume 2. — 2nd ed., corrected. and enlarged. — St. Petersburg: SpetsLit, 2011, pp. 242-250. ISBN 978-5-299-00431-1</mixed-citation><mixed-citation xml:lang="ru">5.	Гансбургский АН, Павлов А.В. Эндотелий. В кн.: Руководство по гистологии : учебное пособие для студентов медицинских вузов и факультетов, аспирантов и слушателей системы дополнительного медицинского образования : в 2 т. / под ред. Р. К. Данилова. Т. 2. — 2-е изд., испр. и доп. — Санкт-Петербург : СпецЛит, 2011, С. 242-250. ISBN 978-5-299-00431-1</mixed-citation></citation-alternatives></ref><ref id="B6"><label>6.</label><citation-alternatives><mixed-citation xml:lang="en">6.	Khlopin NG General Biological and Experimental Foundations of Histology. Publishing House of the USSR Academy of Sciences, 1946.Khlopin NG. Endothelial specificity, regenerative capabilities, and relationships between vascular wall tissues. Archives of Anatomy, Histology, and Embryology, 1958; 35(1): 13–27.</mixed-citation><mixed-citation xml:lang="ru">6.	Хлопин НГ. Общебиологические и экспериментальные основы гистологии. Изд-во Академии Наук СССР, 1946.</mixed-citation></citation-alternatives></ref><ref id="B7"><label>7.</label><citation-alternatives><mixed-citation xml:lang="en">7.	Shevchenko NA. Endothelium of the great vessels of mammals and its place in the tissue system. Archives of Anatomy, Histology and Embryology, 1967; 53(12): 3–18. (In Russ.)</mixed-citation><mixed-citation xml:lang="ru">7.	Khlopin NG. Endothelial specificity, regenerative capabilities, and relationships between vascular wall tissues. Archives of Anatomy, Histology, and Embryology, 1958; 35(1): 13–27.</mixed-citation></citation-alternatives></ref><ref id="B8"><label>8.</label><citation-alternatives><mixed-citation xml:lang="en">8.	Shevchenko NA. Endothelium as a tissue. Proceedings of the 1st Leningrad Medical Institute, 1971; 3: 178–190. (In Russ.)</mixed-citation><mixed-citation xml:lang="ru">8.	Shevchenko NA. Endothelium of the great vessels of mammals and its place in the tissue system. Archives of Anatomy, Histology and Embryology, 1967; 53(12): 3–18. (In Russ.)</mixed-citation></citation-alternatives></ref><ref id="B9"><label>9.</label><citation-alternatives><mixed-citation xml:lang="en">9.	Shevchenko NG. Tissue properties of the endothelium of the main vessels. Archives of Pathology, 1975; (11): 16–23. (In Russ.)</mixed-citation><mixed-citation xml:lang="ru">9.	Shevchenko NA. Endothelium as a tissue. Proceedings of the 1st Leningrad Medical Institute, 1971; 3: 178–190. (In Russ.)</mixed-citation></citation-alternatives></ref><ref id="B10"><label>10.</label><citation-alternatives><mixed-citation xml:lang="en">10.	Mikhailov VP. Classification of tissues and the phenomenon of metaplasia in light of the principle of tissue determination. Archives of Anatomy, Histology and Embryology, 1972; 57(6): 12–32. (In Russ.)</mixed-citation><mixed-citation xml:lang="ru">10.	Shevchenko NG. Tissue properties of the endothelium of the main vessels. Archives of Pathology, 1975; (11): 16–23. (In Russ.)</mixed-citation></citation-alternatives></ref><ref id="B11"><label>11.</label><citation-alternatives><mixed-citation xml:lang="en">11.	Danilov RK, Borovaya TG, Klochkov ND. Experimental histological analysis of histogenesis and reparative tissue regeneration (some results of the 20th century and prospects for further research). Morphology, 2000; 118(4): 7-16. (In Russ.) EDN: MQKGEV</mixed-citation><mixed-citation xml:lang="ru">11.	Mikhailov VP. Classification of tissues and the phenomenon of metaplasia in light of the principle of tissue determination. Archives of Anatomy, Histology and Embryology, 1972; 57(6): 12–32. (In Russ.)</mixed-citation></citation-alternatives></ref><ref id="B12"><label>12.</label><citation-alternatives><mixed-citation xml:lang="en">12.	Danilov RK. General principles of cellular organization, development, and classification of tissues. In: Handbook of Histology / edited by R.K. Danilov. - 2nd ed. - St. Petersburg: "SpetsLit", 2011 - Vol. 1 - Pp. 98-123. ISBN: 9785299004359</mixed-citation><mixed-citation xml:lang="ru">12.	Danilov RK, Borovaya TG, Klochkov ND. Experimental histological analysis of histogenesis and reparative tissue regeneration (some results of the 20th century and prospects for further research). Morphology, 2000; 118(4): 7-16. (In Russ.) EDN: MQKGEV</mixed-citation></citation-alternatives></ref><ref id="B13"><label>13.</label><citation-alternatives><mixed-citation xml:lang="en">13.	Kupriyanov VV, Mironov VA, Mironov AA, Gurina OY. Angiogenesis. Formation, growth, and development of blood vessels. Moscow: NIO "Quartet", 1993. ISBN: 5855730034Sesorova IS, Bedyaev EV, Vavilov PS, Levin SL, Mironov AA. Regeneration of Vascular Endothelium in Different Large Vessels. Int J Mol Sci. 2025;26(2):837. doi:10.3390/ijms26020837 EDN: KTFLIO</mixed-citation><mixed-citation xml:lang="ru">13.	Данилов РК. Общие принципы клеточной организации, развития и классификации тканей. В кн.: Руководство по гистологии / под ред. Р.К. Данилова. – 2-е изд. – СПб.: «СпецЛит», 2011 – Т. 1 – С. 98-123. ISBN: 9785299004359</mixed-citation></citation-alternatives></ref><ref id="B14"><label>14.</label><citation-alternatives><mixed-citation xml:lang="en">14.	Korablev AV, Sesorova IS, Sesorov VV, et al. New Interpretations for Sprouting, Intussusception, Ansiform, and Coalescent Types of Angiogenesis. Int J Mol Sci. 2024;25(16):8575. doi:10.3390/ijms25168575 EDN: IQFCSG</mixed-citation><mixed-citation xml:lang="ru">14.	Куприянов ВВ, Миронов ВА, Миронов АА, Гурина ОЮ. Ангиогенез. Образование, рост и развития кровеносных сосудов. М.: НИО «Квартет», 1993. ISBN: 5855730034</mixed-citation></citation-alternatives></ref><ref id="B15"><label>15.</label><citation-alternatives><mixed-citation xml:lang="en">15.	Larionov A, Hammer CM, Fiedler K, Filgueira L. Dynamics of Endothelial Cell Diversity and Plasticity in Health and Disease. Cells. 2024;13(15):1276. doi:10.3390/cells13151276 EDN: EVVYLC</mixed-citation><mixed-citation xml:lang="ru">15.	Sesorova IS, Bedyaev EV, Vavilov PS, Levin SL, Mironov AA. Regeneration of Vascular Endothelium in Different Large Vessels. Int J Mol Sci. 2025;26(2):837. doi:10.3390/ijms26020837 EDN: KTFLIO</mixed-citation></citation-alternatives></ref><ref id="B16"><label>16.</label><citation-alternatives><mixed-citation xml:lang="en">16.	Maximow AA. Bindegewebe und blutbildendes Gewebe. Handb. d. mikr. Anat. d. Menschen. Herausgegeb. von W. v. Mollendorf. Bd. I/II, Berlin; 1927.</mixed-citation><mixed-citation xml:lang="ru">16.	Korablev AV, Sesorova IS, Sesorov VV, et al. New Interpretations for Sprouting, Intussusception, Ansiform, and Coalescent Types of Angiogenesis. Int J Mol Sci. 2024;25(16):8575. doi:10.3390/ijms25168575 EDN: IQFCSG</mixed-citation></citation-alternatives></ref><ref id="B17"><label>17.</label><citation-alternatives><mixed-citation xml:lang="en">17.	Maximow AA. Morphology of the Mesenchymal Reactions. Archives of Pathology and Laboratory Medicine, 1927; 4: 557-606.</mixed-citation><mixed-citation xml:lang="ru">17.	Larionov A, Hammer CM, Fiedler K, Filgueira L. Dynamics of Endothelial Cell Diversity and Plasticity in Health and Disease. Cells. 2024;13(15):1276. doi:10.3390/cells13151276 EDN: EVVYLC</mixed-citation></citation-alternatives></ref><ref id="B18"><label>18.</label><citation-alternatives><mixed-citation xml:lang="en">18.	Aschoff L, Kiyono K. Zur Frage der grossen Mononucleären. Folia Haem. 1913; 15: 385–390.</mixed-citation><mixed-citation xml:lang="ru">18.	Maximow AA. Bindegewebe und blutbildendes Gewebe. Handb. d. mikr. Anat. d. Menschen. Herausgegeb. von W. v. Mollendorf. Bd. I/II, Berlin; 1927.</mixed-citation></citation-alternatives></ref><ref id="B19"><label>19.</label><citation-alternatives><mixed-citation xml:lang="en">19.	Kiyono K. Zur Frage der histiozytaren Blutzellen. Folia Haematol. (Frankf.), 1914; 18: 149–170.</mixed-citation><mixed-citation xml:lang="ru">19.	Maximow AA. Morphology of the Mesenchymal Reactions. Archives of Pathology and Laboratory Medicine, 1927; 4: 557-606.</mixed-citation></citation-alternatives></ref><ref id="B20"><label>20.</label><citation-alternatives><mixed-citation xml:lang="en">20.	Aschoff L. Das retikulo-endotheliale system und seine Beziehungen zur Gallenfarbstoffbildung. Munch. Med. Wochenschr. 1922; 69: 1352–1356.</mixed-citation><mixed-citation xml:lang="ru">20.	Aschoff L, Kiyono K. Zur Frage der grossen Mononucleären. Folia Haem. 1913; 15: 385–390.</mixed-citation></citation-alternatives></ref><ref id="B21"><label>21.</label><citation-alternatives><mixed-citation xml:lang="en">21.	Aschoff L. Das reticulo-endotheliale System. In: Ergebnisse der Inneren Medizin und Kinderheilkunde, 1924; 2-118.</mixed-citation><mixed-citation xml:lang="ru">21.	Kiyono K. Zur Frage der histiozytaren Blutzellen. Folia Haematol. (Frankf.), 1914; 18: 149–170.</mixed-citation></citation-alternatives></ref><ref id="B22"><label>22.</label><citation-alternatives><mixed-citation xml:lang="en">22.	Aschoff L. Lectures on Pathology. New-York, P.B. Hoeber, 1924; 1-33.</mixed-citation><mixed-citation xml:lang="ru">22.	Aschoff L. Das retikulo-endotheliale system und seine Beziehungen zur Gallenfarbstoffbildung. Munch. Med. Wochenschr. 1922; 69: 1352–1356.</mixed-citation></citation-alternatives></ref><ref id="B23"><label>23.</label><citation-alternatives><mixed-citation xml:lang="en">23.	Aschoff L. On the mesenchyme and inflammatory cells. In the book: Modern problems of pathology. A series of reports read in the USSR in the autumn of 1930. State Medical Publishing House, Moscow, Leningrad, 1930. - 7-13.</mixed-citation><mixed-citation xml:lang="ru">23.	Aschoff L. Das reticulo-endotheliale System. In: Ergebnisse der Inneren Medizin und Kinderheilkunde, 1924; 2-118.</mixed-citation></citation-alternatives></ref><ref id="B24"><label>24.</label><citation-alternatives><mixed-citation xml:lang="en">24.	Metchnicoff E. Leçons sur la pathologie comparée de l'inflammation : faites à l'Institut Pasteur en 1891; Paris : Masson.</mixed-citation><mixed-citation xml:lang="ru">24.	Aschoff L. Lectures on Pathology. New-York, P.B. Hoeber, 1924; 1-33.</mixed-citation></citation-alternatives></ref><ref id="B25"><label>25.</label><citation-alternatives><mixed-citation xml:lang="en">25.	Metchnicoff E. L'immunité dans les maladies infectieuses. Paris, Masson; 1892.</mixed-citation><mixed-citation xml:lang="ru">25.	Ашофф Л. О мезенхиме и воспалительных клетках. В кн.: Современные проблемы патологии. Цикл докладов, читанных в СССР осенью 1930 г. Государственное медицинское издательство, М., Л., 1930. - 7-13.</mixed-citation></citation-alternatives></ref><ref id="B26"><label>26.</label><citation-alternatives><mixed-citation xml:lang="en">26.	van Furth R, Cohn Z A, Hirsch J G et al. Langevoort The mononuclear phagocyte system: a new classification of macrophages, monocytes, and their precursor cells. Bull World Health Organ 1972; 46(6):845-52.</mixed-citation><mixed-citation xml:lang="ru">26.	Metchnicoff E. Leçons sur la pathologie comparée de l'inflammation : faites à l'Institut Pasteur en 1891; Paris : Masson.</mixed-citation></citation-alternatives></ref><ref id="B27"><label>27.</label><citation-alternatives><mixed-citation xml:lang="en">27.	Anichkov N.N. The doctrine of the reticuloendothelial system. Moscow; Leningrad: State Publishing House, 1930. — 336 p.</mixed-citation><mixed-citation xml:lang="ru">27.	Metchnicoff E. L'immunité dans les maladies infectieuses. Paris, Masson; 1892.</mixed-citation></citation-alternatives></ref><ref id="B28"><label>28.</label><citation-alternatives><mixed-citation xml:lang="en">28.	Seternes T, Sørensen K, Smedsrød B. Scavenger endothelial cells of vertebrates: a nonperipheral leukocyte system for high-capacity elimination of waste macromolecules. Proc Natl Acad Sci U S A. 2002;99(11):7594-7597. doi:10.1073/pnas.102173299</mixed-citation><mixed-citation xml:lang="ru">28.	van Furth R, Cohn Z A, Hirsch J G et al. Langevoort The mononuclear phagocyte system: a new classification of macrophages, monocytes, and their precursor cells. Bull World Health Organ 1972; 46(6):845-52.</mixed-citation></citation-alternatives></ref><ref id="B29"><label>29.</label><citation-alternatives><mixed-citation xml:lang="en">29.	Enomoto K, Nishikawa Y, Omori Y, et al. Cell biology and pathology of liver sinusoidal endothelial cells. Med Electron Microsc. 2004;37(4):208-215. doi:10.1007/s00795-004-0261-4</mixed-citation><mixed-citation xml:lang="ru">29.	Аничков НН. Учение о ретикуло-эндотелиальной системе. М. ; Л. : Гос. изд-во, 1930. — 336 с.</mixed-citation></citation-alternatives></ref><ref id="B30"><label>30.</label><citation-alternatives><mixed-citation xml:lang="en">30.	Kamimoto M, Rung-Ruangkijkrai T, Iwanaga T. Uptake ability of hepatic sinusoidal endothelial cells and enhancement by lipopolysaccharide. Biomed Res. 2005;26(3):99-107. doi:10.2220/biomedres.26.99</mixed-citation><mixed-citation xml:lang="ru">30.	Seternes T, Sørensen K, Smedsrød B. Scavenger endothelial cells of vertebrates: a nonperipheral leukocyte system for high-capacity elimination of waste macromolecules. Proc Natl Acad Sci U S A. 2002;99(11):7594-7597. doi:10.1073/pnas.102173299</mixed-citation></citation-alternatives></ref><ref id="B31"><label>31.</label><citation-alternatives><mixed-citation xml:lang="en">31.	Аравийская ДД. Интрамуральные воспалительные разрастания эндотелия магистральных вен. Автореф. дис. канд. мед. наук. Л., 1971.</mixed-citation><mixed-citation xml:lang="ru">31.	Enomoto K, Nishikawa Y, Omori Y, et al. Cell biology and pathology of liver sinusoidal endothelial cells. Med Electron Microsc. 2004;37(4):208-215. doi:10.1007/s00795-004-0261-4</mixed-citation></citation-alternatives></ref><ref id="B32"><label>32.</label><citation-alternatives><mixed-citation xml:lang="en">32.	Гололобов ВГ. Автореф. дис. канд. мед. наук. Л. Эндовазальные посттравматические разрастания эндотелия яремной вены. Автореф. дис. канд. мед. наук. Л., 1971.</mixed-citation><mixed-citation xml:lang="ru">32.	Kamimoto M, Rung-Ruangkijkrai T, Iwanaga T. Uptake ability of hepatic sinusoidal endothelial cells and enhancement by lipopolysaccharide. Biomed Res. 2005;26(3):99-107. doi:10.2220/biomedres.26.99</mixed-citation></citation-alternatives></ref><ref id="B33"><label>33.</label><citation-alternatives><mixed-citation xml:lang="en">33.	Rakocevic J, Orlic D, Mitrovic-Ajtic O, et al. Endothelial cell markers from clinician's perspective. Experimental and Molecular Pathology. 2017; 102(2): 303-313. DOI: 10.1016/j.yexmp.2017.02.005 EDN: YYBBDL</mixed-citation><mixed-citation xml:lang="ru">33.	Аравийская ДД. Интрамуральные воспалительные разрастания эндотелия магистральных вен. Автореф. дис. канд. мед. наук. Л., 1971.</mixed-citation></citation-alternatives></ref><ref id="B34"><label>34.</label><citation-alternatives><mixed-citation xml:lang="en">34.	Goncharov NV, Popova PI, Avdonin PP, et al. Endothelial cell markers in health and disease. Biological membranes. 2020; 37(1): 3-21. (In Russ.) doi:10.31857/S0233475519040054 EDN: RULXBT</mixed-citation><mixed-citation xml:lang="ru">34.	Гололобов ВГ. Автореф. дис. канд. мед. наук. Л. Эндовазальные посттравматические разрастания эндотелия яремной вены. Автореф. дис. канд. мед. наук. Л., 1971.</mixed-citation></citation-alternatives></ref><ref id="B35"><label>35.</label><citation-alternatives><mixed-citation xml:lang="en">35.	Bessonnard S, De Mot L, Gonze D, et al. Gata6, Nanog and Erk signaling control cell fate in the inner cell mass through a tristable regulatory network. Development. 2014;141(19):3637-3648. doi:10.1242/dev.109678</mixed-citation><mixed-citation xml:lang="ru">35.	Rakocevic J, Orlic D, Mitrovic-Ajtic O, et al. Endothelial cell markers from clinician's per-spective. Experimental and Molecular Pathology. 2017; 102(2): 303-313. DOI: 10.1016/j.yexmp.2017.02.005 EDN: YYBBDL</mixed-citation></citation-alternatives></ref><ref id="B36"><label>36.</label><citation-alternatives><mixed-citation xml:lang="en">36.	Hendrickson CL, Blitz IL, Hussein A, et al. Foxi2 and Sox3 are master regulators controlling ectoderm germ layer specification. bioRxiv [Preprint]. 2025 Jan 9:2025.01.09.632114. doi: 10.1101/2025.01.09.632114. Update in: PLoS Biol. 2025 Nov 4;23(11):e3003476. doi:10.1371/journal.pbio.3003476</mixed-citation><mixed-citation xml:lang="ru">36.	Goncharov NV, Popova PI, Avdonin PP, et al. Endothelial cell markers in health and disease. Biological membranes. 2020; 37(1): 3-21. (In Russ.) doi:10.31857/S0233475519040054 EDN: RULXBT</mixed-citation></citation-alternatives></ref><ref id="B37"><label>37.</label><citation-alternatives><mixed-citation xml:lang="en">37.	Teo AK, Arnold SJ, Trotter MW, et al. Pluripotency factors regulate definitive endoderm specification through eomesodermin. Genes Dev. 2011;25(3):238-250. doi:10.1101/gad.607311 EDN: OAOCJZ</mixed-citation><mixed-citation xml:lang="ru">37.	Bessonnard S, De Mot L, Gonze D, et al. Gata6, Nanog and Erk signaling control cell fate in the inner cell mass through a tristable regulatory network. Development. 2014;141(19):3637-3648. doi:10.1242/dev.109678</mixed-citation></citation-alternatives></ref><ref id="B38"><label>38.</label><citation-alternatives><mixed-citation xml:lang="en">38.	Lewis SL, Tam PP. Definitive endoderm of the mouse embryo: formation, cell fates, and morphogenetic function. Dev Dyn. 2006;235(9):2315-2329. doi:10.1002/dvdy.20846</mixed-citation><mixed-citation xml:lang="ru">38.	Hendrickson CL, Blitz IL, Hussein A, et al. Foxi2 and Sox3 are master regulators controlling ectoderm germ layer specification. bioRxiv [Preprint]. 2025 Jan 9:2025.01.09.632114. doi: 10.1101/2025.01.09.632114. Update in: PLoS Biol. 2025 Nov 4;23(11):e3003476. doi:10.1371/journal.pbio.3003476</mixed-citation></citation-alternatives></ref><ref id="B39"><label>39.</label><citation-alternatives><mixed-citation xml:lang="en">39. Nord J, Schill D, Pulakanti K, et al. The transcription factor FoxO1 is required for the establishment of the human definitive endoderm, bioRxiv 2020.12.22.423976; doi:10.1101/2020.12.22.423976</mixed-citation><mixed-citation xml:lang="ru">39.	Teo AK, Arnold SJ, Trotter MW, et al. Pluripotency factors regulate definitive endoderm specification through eomesodermin. Genes Dev. 2011;25(3):238-250. doi:10.1101/gad.607311 EDN: OAOCJZ</mixed-citation></citation-alternatives></ref><ref id="B40"><label>40.</label><citation-alternatives><mixed-citation xml:lang="en">40.	Arnold SJ, Hofmann UK, Bikoff EK, Robertson EJ. Pivotal roles for eomesodermin during axis formation, epithelium-to-mesenchyme transition and endoderm specification in the mouse. Development. 2008;135(3):501-511. doi:10.1242/dev.014357</mixed-citation><mixed-citation xml:lang="ru">40.	Lewis SL, Tam PP. Definitive endoderm of the mouse embryo: formation, cell fates, and morphogenetic function. Dev Dyn. 2006;235(9):2315-2329. doi:10.1002/dvdy.20846</mixed-citation></citation-alternatives></ref><ref id="B41"><label>41.</label><citation-alternatives><mixed-citation xml:lang="en">41.	Lolas M, Valenzuela PD, Tjian R, Liu Z. Charting Brachyury-mediated developmental pathways during early mouse embryogenesis. Proc Natl Acad Sci U S A. 2014;111(12):4478-4483. doi:10.1073/pnas.1402612111</mixed-citation><mixed-citation xml:lang="ru">41. Nord J, Schill D, Pulakanti K, et al. The transcription factor FoxO1 is required for the establishment of the human definitive endoderm, bioRxiv 2020.12.22.423976; doi:10.1101/2020.12.22.423976</mixed-citation></citation-alternatives></ref><ref id="B42"><label>42.</label><citation-alternatives><mixed-citation xml:lang="en">42.	Beddington RS, Rashbass P, Wilson V. Brachyury. A gene affecting mouse gastrulation and early organogenesis. Dev Suppl. 1992;157-165.</mixed-citation><mixed-citation xml:lang="ru">42.	Arnold SJ, Hofmann UK, Bikoff EK, Robertson EJ. Pivotal roles for eomesodermin during axis formation, epithelium-to-mesenchyme transition and endoderm specification in the mouse. Development. 2008;135(3):501-511. doi:10.1242/dev.014357</mixed-citation></citation-alternatives></ref><ref id="B43"><label>43.</label><citation-alternatives><mixed-citation xml:lang="en">43.	Stott D, Kispert A, Herrmann BG. Rescue of the tail defect of Brachyury mice. Genes Dev. 1993;7(2):197-203. doi:10.1101/gad.7.2.197</mixed-citation><mixed-citation xml:lang="ru">43.	Lolas M, Valenzuela PD, Tjian R, Liu Z. Charting Brachyury-mediated developmental pathways during early mouse embryogenesis. Proc Natl Acad Sci U S A. 2014;111(12):4478-4483. doi:10.1073/pnas.1402612111</mixed-citation></citation-alternatives></ref><ref id="B44"><label>44.</label><citation-alternatives><mixed-citation xml:lang="en">44.	Conlon FL, Smith JC. Interference with brachyury function inhibits convergent extension, causes apoptosis, and reveals separate requirements in the FGF and activin signalling pathways. Dev Biol. 1999;213(1):85-100. doi:10.1006/dbio.1999.9330</mixed-citation><mixed-citation xml:lang="ru">44.	Beddington RS, Rashbass P, Wilson V. Brachyury. A gene affecting mouse gastrulation and early organogenesis. Dev Suppl. 1992;157-165.</mixed-citation></citation-alternatives></ref><ref id="B45"><label>45.</label><citation-alternatives><mixed-citation xml:lang="en">45.	Chan SS, Shi X, Toyama A, et al. Mesp1 patterns mesoderm into cardiac, hematopoietic, or skeletal myogenic progenitors in a context-dependent manner. Cell Stem Cell. 2013;12(5):587-601. doi:10.1016/j.stem.2013.03.004</mixed-citation><mixed-citation xml:lang="ru">45.	Stott D, Kispert A, Herrmann BG. Rescue of the tail defect of Brachyury mice. Genes Dev. 1993;7(2):197-203. doi:10.1101/gad.7.2.197</mixed-citation></citation-alternatives></ref><ref id="B46"><label>46.</label><citation-alternatives><mixed-citation xml:lang="en">46.	Soibam B, Benham A, Kim J, et al. Genome-Wide Identification of MESP1 Targets Demonstrates Primary Regulation Over Mesendoderm Gene Activity. Stem Cells. 2015;33(11):3254-3265. doi:10.1002/stem.2111</mixed-citation><mixed-citation xml:lang="ru">46.	Conlon FL, Smith JC. Interference with brachyury function inhibits convergent extension, causes apoptosis, and reveals separate requirements in the FGF and activin signalling pathways. Dev Biol. 1999;213(1):85-100. doi:10.1006/dbio.1999.9330</mixed-citation></citation-alternatives></ref><ref id="B47"><label>47.</label><citation-alternatives><mixed-citation xml:lang="en">47.	Ferrer-Vaquer A, Viotti M, Hadjantonakis AK. Transitions between epithelial and mesenchymal states and the morphogenesis of the early mouse embryo. Cell Adh Migr. 2010;4(3):447-457. doi:10.4161/cam.4.3.10771</mixed-citation><mixed-citation xml:lang="ru">47.	Chan SS, Shi X, Toyama A, et al. Mesp1 patterns mesoderm into cardiac, hematopoietic, or skeletal myogenic progenitors in a context-dependent manner. Cell Stem Cell. 2013;12(5):587-601. doi:10.1016/j.stem.2013.03.004</mixed-citation></citation-alternatives></ref><ref id="B48"><label>48.</label><citation-alternatives><mixed-citation xml:lang="en">48.	Oh SY, Kim JY, Park C. The ETS Factor, ETV2: a Master Regulator for Vascular Endothelial Cell Development. Mol Cells. 2015;38(12):1029-1036. doi:10.14348/molcells.2015.0331</mixed-citation><mixed-citation xml:lang="ru">48.	Soibam B, Benham A, Kim J, et al. Genome-Wide Identification of MESP1 Targets Demonstrates Primary Regulation Over Mesendoderm Gene Activity. Stem Cells. 2015;33(11):3254-3265. doi:10.1002/stem.2111</mixed-citation></citation-alternatives></ref><ref id="B49"><label>49.</label><citation-alternatives><mixed-citation xml:lang="en">49.	Morita R, Suzuki M, Kasahara H, et al. ETS transcription factor ETV2 directly converts human fibroblasts into functional endothelial cells. Proc Natl Acad Sci U S A. 2015;112(1):160-165. doi:10.1073/pnas.1413234112</mixed-citation><mixed-citation xml:lang="ru">49.	Ferrer-Vaquer A, Viotti M, Hadjantonakis AK. Transitions between epithelial and mesenchymal states and the morphogenesis of the early mouse embryo. Cell Adh Migr. 2010;4(3):447-457. doi:10.4161/cam.4.3.10771</mixed-citation></citation-alternatives></ref><ref id="B50"><label>50.</label><citation-alternatives><mixed-citation xml:lang="en">50.	Koyano-Nakagawa N, Shi X, Rasmussen TL, et al. Feedback Mechanisms Regulate Ets Variant 2 (Etv2) Gene Expression and Hematoendothelial Lineages. J Biol Chem. 2015;290(47):28107-28119. doi:10.1074/jbc.M115.662197</mixed-citation><mixed-citation xml:lang="ru">50.	Oh SY, Kim JY, Park C. The ETS Factor, ETV2: a Master Regulator for Vascular Endothelial Cell Development. Mol Cells. 2015;38(12):1029-1036. doi:10.14348/molcells.2015.0331</mixed-citation></citation-alternatives></ref><ref id="B51"><label>51.</label><citation-alternatives><mixed-citation xml:lang="en">51.	Wang YJ, Huang J, Liu W, et al. IP3R-mediated Ca2+ signals govern hematopoietic and cardiac divergence of Flk1+ cells via the calcineurin-NFATc3-Etv2 pathway. J Mol Cell Biol. 2017;9(4):274-288. doi:10.1093/jmcb/mjx014</mixed-citation><mixed-citation xml:lang="ru">51.	Morita R, Suzuki M, Kasahara H, et al. ETS transcription factor ETV2 directly converts human fibroblasts into functional endothelial cells. Proc Natl Acad Sci U S A. 2015;112(1):160-165. doi:10.1073/pnas.1413234112</mixed-citation></citation-alternatives></ref><ref id="B52"><label>52.</label><citation-alternatives><mixed-citation xml:lang="en">52.	Ema M, Rossant J. Cell fate decisions in early blood vessel formation. Trends Cardiovasc Med. 2003;13(6):254-259. doi:10.1016/s1050-1738(03)00105-1</mixed-citation><mixed-citation xml:lang="ru">52.	Koyano-Nakagawa N, Shi X, Rasmussen TL, et al. Feedback Mechanisms Regulate Ets Variant 2 (Etv2) Gene Expression and Hematoendothelial Lineages. J Biol Chem. 2015;290(47):28107-28119. doi:10.1074/jbc.M115.662197</mixed-citation></citation-alternatives></ref><ref id="B53"><label>53.</label><citation-alternatives><mixed-citation xml:lang="en">53.	De Val S, Black BL. Transcriptional control of endothelial cell development. Dev Cell. 2009;16(2):180-195. doi:10.1016/j.devcel.2009.01.014</mixed-citation><mixed-citation xml:lang="ru">53.	Wang YJ, Huang J, Liu W, et al. IP3R-mediated Ca2+ signals govern hematopoietic and cardiac divergence of Flk1+ cells via the calcineurin-NFATc3-Etv2 pathway. J Mol Cell Biol. 2017;9(4):274-288. doi:10.1093/jmcb/mjx014</mixed-citation></citation-alternatives></ref><ref id="B54"><label>54.</label><citation-alternatives><mixed-citation xml:lang="en">54.	Park C, Kim TM, Malik AB. Transcriptional regulation of endothelial cell and vascular development. Circ Res. 2013;112(10):1380-1400. doi:10.1161/CIRCRESAHA.113.301078</mixed-citation><mixed-citation xml:lang="ru">54.	Ema M, Rossant J. Cell fate decisions in early blood vessel formation. Trends Cardiovasc Med. 2003;13(6):254-259. doi:10.1016/s1050-1738(03)00105-1</mixed-citation></citation-alternatives></ref><ref id="B55"><label>55.</label><citation-alternatives><mixed-citation xml:lang="en">55.	Rousseau S, Houle F, Kotanides H, et al. Vascular endothelial growth factor (VEGF)-driven actin-based motility is mediated by VEGFR2 and requires concerted activation of stress-activated protein kinase 2 (SAPK2/p38) and geldanamycin-sensitive phosphorylation of focal adhesion kinase. J Biol Chem. 2000;275(14):10661-10672. doi:10.1074/jbc.275.14.10661 EDN: YECWHY</mixed-citation><mixed-citation xml:lang="ru">55.	De Val S, Black BL. Transcriptional control of endothelial cell development. Dev Cell. 2009;16(2):180-195. doi:10.1016/j.devcel.2009.01.014</mixed-citation></citation-alternatives></ref><ref id="B56"><label>56.</label><citation-alternatives><mixed-citation xml:lang="en">56.	Abhinand CS, Raju R, Soumya SJ, et al. VEGF-A/VEGFR2 signaling network in endothelial cells relevant to angiogenesis. J Cell Commun Signal. 2016;10(4):347-354. doi:10.1007/s12079-016-0352-8 EDN: NTNUUY</mixed-citation><mixed-citation xml:lang="ru">56.	Park C, Kim TM, Malik AB. Transcriptional regulation of endothelial cell and vascular development. Circ Res. 2013;112(10):1380-1400. doi:10.1161/CIRCRESAHA.113.301078</mixed-citation></citation-alternatives></ref><ref id="B57"><label>57.</label><citation-alternatives><mixed-citation xml:lang="en">57.	Greenspan LJ, Weinstein BM. To be or not to be: endothelial cell plasticity in development, repair, and disease. Angiogenesis. 2021;24(2):251-269. doi:10.1007/s10456-020-09761-7 EDN: KWGURR</mixed-citation><mixed-citation xml:lang="ru">57.	Rousseau S, Houle F, Kotanides H, et al. Vascular endothelial growth factor (VEGF)-driven actin-based motility is mediated by VEGFR2 and requires concerted activation of stress-activated protein kinase 2 (SAPK2/p38) and geldanamycin-sensitive phosphorylation of focal adhesion kinase. J Biol Chem. 2000;275(14):10661-10672. doi:10.1074/jbc.275.14.10661 EDN: YECWHY</mixed-citation></citation-alternatives></ref><ref id="B58"><label>58.</label><citation-alternatives><mixed-citation xml:lang="en">58.	Chanda B, Ditadi A, Iscove NN, Keller G. Retinoic acid signaling is essential for embryonic hematopoietic stem cell development. Cell. 2013;155(1):215-227. doi:10.1016/j.cell.2013.08.055</mixed-citation><mixed-citation xml:lang="ru">58.	Abhinand CS, Raju R, Soumya SJ, et al. VEGF-A/VEGFR2 signaling network in endothelial cells relevant to angiogenesis. J Cell Commun Signal. 2016;10(4):347-354. doi:10.1007/s12079-016-0352-8 EDN: NTNUUY</mixed-citation></citation-alternatives></ref><ref id="B59"><label>59.</label><citation-alternatives><mixed-citation xml:lang="en">59.	Alsukari SH, Ng HT, Lang L, et al. Dynamic WT1 expression during gastrulation specifies peritoneal smooth muscle fate independently of mesothelial fate. Development. 2025;152(13):dev204332. doi:10.1242/dev.204332 EDN: SFGVDD</mixed-citation><mixed-citation xml:lang="ru">59.	Greenspan LJ, Weinstein BM. To be or not to be: endothelial cell plasticity in development, repair, and disease. Angiogenesis. 2021;24(2):251-269. doi:10.1007/s10456-020-09761-7 EDN: KWGURR</mixed-citation></citation-alternatives></ref><ref id="B60"><label>60.</label><citation-alternatives><mixed-citation xml:lang="en">60.	Wilm TP, Tanton H, Mutter F, et al. Restricted differentiative capacity of Wt1-expressing peritoneal mesothelium in postnatal and adult mice. Sci Rep. 2021;11(1):15940. doi:10.1038/s41598-021-95380-1 EDN: LAZAPB</mixed-citation><mixed-citation xml:lang="ru">60.	Chanda B, Ditadi A, Iscove NN, Keller G. Retinoic acid signaling is essential for embryonic hematopoietic stem cell development. Cell. 2013;155(1):215-227. doi:10.1016/j.cell.2013.08.055</mixed-citation></citation-alternatives></ref><ref id="B61"><label>61.</label><citation-alternatives><mixed-citation xml:lang="en">61.	Prummel KD, Crowell HL, Nieuwenhuize S, et al. Hand2 delineates mesothelium progenitors and is reactivated in mesothelioma. Nat Commun. 2022;13(1):1677. doi:10.1038/s41467-022-29311-7 EDN: DXUEEH</mixed-citation><mixed-citation xml:lang="ru">61.	Alsukari SH, Ng HT, Lang L, et al. Dynamic WT1 expression during gastrulation specifies peritoneal smooth muscle fate independently of mesothelial fate. Development. 2025;152(13):dev204332. doi:10.1242/dev.204332 EDN: SFGVDD</mixed-citation></citation-alternatives></ref><ref id="B62"><label>62.</label><citation-alternatives><mixed-citation xml:lang="en">62.	Donovan MJ, Natoli TA, Sainio K, et al. Initial differentiation of the metanephric mesenchyme is independent of WT1 and the ureteric bud. Dev Genet. 1999;24(3-4):252-262. doi:10.1002/(SICI)1520-6408(1999)24:3/4&lt;252::AID-DVG8&gt;3.0.CO;2-K</mixed-citation><mixed-citation xml:lang="ru">62.	Wilm TP, Tanton H, Mutter F, et al. Restricted differentiative capacity of Wt1-expressing peritoneal mesothelium in postnatal and adult mice. Sci Rep. 2021;11(1):15940. doi:10.1038/s41598-021-95380-1 EDN: LAZAPB</mixed-citation></citation-alternatives></ref><ref id="B63"><label>63.</label><citation-alternatives><mixed-citation xml:lang="en">63.	Kann M, Bae E, Lenz MO, et al. WT1 targets Gas1 to maintain nephron progenitor cells by modulating FGF signals. Development. 2015;142(7):1254-1266. doi:10.1242/dev.119735</mixed-citation><mixed-citation xml:lang="ru">63.	Prummel KD, Crowell HL, Nieuwenhuize S, et al. Hand2 delineates mesothelium progenitors and is reactivated in mesothelioma. Nat Commun. 2022;13(1):1677. doi:10.1038/s41467-022-29311-7 EDN: DXUEEH</mixed-citation></citation-alternatives></ref><ref id="B64"><label>64.</label><citation-alternatives><mixed-citation xml:lang="en">64.	Gao X, Chen X, Taglienti M, et al. Angioblast-mesenchyme induction of early kidney development is mediated by Wt1 and Vegfa. Development. 2005;132(24):5437-5449. doi:10.1242/dev.02095</mixed-citation><mixed-citation xml:lang="ru">64.	Donovan MJ, Natoli TA, Sainio K, et al. Initial differentiation of the metanephric mesenchyme is independent of WT1 and the ureteric bud. Dev Genet. 1999;24(3-4):252-262. doi:10.1002/(SICI)1520-6408(1999)24:3/4&lt;252::AID-DVG8&gt;3.0.CO;2-K</mixed-citation></citation-alternatives></ref><ref id="B65"><label>65.</label><citation-alternatives><mixed-citation xml:lang="en">65.	Davies JA, Fisher CE. Genes and proteins in renal development. Exp Nephrol. 2002;10(2):102-113. doi:10.1159/000049905</mixed-citation><mixed-citation xml:lang="ru">65.	Kann M, Bae E, Lenz MO, et al. WT1 targets Gas1 to maintain nephron progenitor cells by modulating FGF signals. Development. 2015;142(7):1254-1266. doi:10.1242/dev.119735</mixed-citation></citation-alternatives></ref><ref id="B66"><label>66.</label><citation-alternatives><mixed-citation xml:lang="en">66.	Joo-Seop Park, Andrew P. McMahon. Transcriptional Regulation of the Nephrogenic Mesenchyme and Its Progeny, Editor(s): Melissa H. Little, Kidney Development, Disease, Repair and Regeneration, Academic Press, 2016: 67-74. ISBN 9780128001028, doi:10.1016/B978-0-12-800102-8.00006-0 ISBN: 978-0-12-800102-8</mixed-citation><mixed-citation xml:lang="ru">66.	Gao X, Chen X, Taglienti M, et al. Angioblast-mesenchyme induction of early kidney development is mediated by Wt1 and Vegfa. Development. 2005;132(24):5437-5449. doi:10.1242/dev.02095</mixed-citation></citation-alternatives></ref><ref id="B67"><label>67.</label><citation-alternatives><mixed-citation xml:lang="en">67.	Mattonet K, Riemslagh FW, Guenther S, et al. Endothelial versus pronephron fate decision is modulated by the transcription factors Cloche/Npas4l, Tal1, and Lmo2. Sci Adv. 2022;8(35):eabn2082. doi:10.1126/sciadv.abn2082 EDN: WVTHSK</mixed-citation><mixed-citation xml:lang="ru">67.	Davies JA, Fisher CE. Genes and proteins in renal development. Exp Nephrol. 2002;10(2):102-113. doi:10.1159/000049905</mixed-citation></citation-alternatives></ref><ref id="B68"><label>68.</label><citation-alternatives><mixed-citation xml:lang="en">68.	Eckert RL, Adhikary G, Young CA, et al. AP1 transcription factors in epidermal differentiation and skin cancer. J Skin Cancer. 2013;2013:537028. doi:10.1155/2013/537028</mixed-citation><mixed-citation xml:lang="ru">68.	Joo-Seop Park, Andrew P. McMahon. Transcriptional Regulation of the Nephrogenic Mesenchyme and Its Progeny, Editor(s): Melissa H. Little, Kidney Development, Disease, Repair and Regeneration, Academic Press, 2016: 67-74. ISBN 9780128001028, doi:10.1016/B978-0-12-800102-8.00006-0 ISBN: 978-0-12-800102-8</mixed-citation></citation-alternatives></ref><ref id="B69"><label>69.</label><citation-alternatives><mixed-citation xml:lang="en">69.	Nakamura Y, Kawachi Y, Xu X, et al. The combination of ubiquitous transcription factors AP-1 and Sp1 directs keratinocyte-specific and differentiation-specific gene expression in vitro. Exp Dermatol. 2007;16(2):143-150. doi:10.1111/j.1600-0625.2006.00528.x</mixed-citation><mixed-citation xml:lang="ru">69.	Mattonet K, Riemslagh FW, Guenther S, et al. Endothelial versus pronephron fate decision is modulated by the transcription factors Cloche/Npas4l, Tal1, and Lmo2. Sci Adv. 2022;8(35):eabn2082. doi:10.1126/sciadv.abn2082 EDN: WVTHSK</mixed-citation></citation-alternatives></ref><ref id="B70"><label>70.</label><citation-alternatives><mixed-citation xml:lang="en">70.	Prowse DM, Bolgan L, Molnár A, Dotto GP. Involvement of the Sp3 transcription factor in induction of p21Cip1/WAF1 in keratinocyte differentiation. J Biol Chem. 1997;272(2):1308-1314. doi:10.1074/jbc.272.2.1308</mixed-citation><mixed-citation xml:lang="ru">70.	Eckert RL, Adhikary G, Young CA, et al. AP1 transcription factors in epidermal differentiation and skin cancer. J Skin Cancer. 2013;2013:537028. doi:10.1155/2013/537028</mixed-citation></citation-alternatives></ref><ref id="B71"><label>71.</label><citation-alternatives><mixed-citation xml:lang="en">71.	Ogaki S, Morooka M, Otera K, Kume S. A cost-effective system for differentiation of intestinal epithelium from human induced pluripotent stem cells. Sci Rep. 2015;5:17297. doi:10.1038/srep17297</mixed-citation><mixed-citation xml:lang="ru">71.	Nakamura Y, Kawachi Y, Xu X, et al. The combination of ubiquitous transcription factors AP-1 and Sp1 directs keratinocyte-specific and differentiation-specific gene expression in vitro. Exp Dermatol. 2007;16(2):143-150. doi:10.1111/j.1600-0625.2006.00528.x</mixed-citation></citation-alternatives></ref><ref id="B72"><label>72.</label><citation-alternatives><mixed-citation xml:lang="en">72.	Viotti M, Nowotschin S, Hadjantonakis AK. SOX17 links gut endoderm morphogenesis and germ layer segregation. Nat Cell Biol. 2014;16(12):1146-1156. doi:10.1038/ncb3070</mixed-citation><mixed-citation xml:lang="ru">72.	Prowse DM, Bolgan L, Molnár A, Dotto GP. Involvement of the Sp3 transcription factor in induction of p21Cip1/WAF1 in keratinocyte differentiation. J Biol Chem. 1997;272(2):1308-1314. doi:10.1074/jbc.272.2.1308</mixed-citation></citation-alternatives></ref><ref id="B73"><label>73.</label><citation-alternatives><mixed-citation xml:lang="en">73.	Dixit R, Ai X, Fine A. Derivation of lung mesenchymal lineages from the fetal mesothelium requires hedgehog signaling for mesothelial cell entry. Development. 2013;140(21):4398-4406. doi:10.1242/dev.098079</mixed-citation><mixed-citation xml:lang="ru">73.	Ogaki S, Morooka M, Otera K, Kume S. A cost-effective system for differentiation of intestinal epithelium from human induced pluripotent stem cells. Sci Rep. 2015;5:17297. doi:10.1038/srep17297</mixed-citation></citation-alternatives></ref><ref id="B74"><label>74.</label><citation-alternatives><mixed-citation xml:lang="en">74.	Mohammadnia A, Yaqubi M, Pourasgari F, et al. Signaling and Gene Regulatory Networks Governing Definitive Endoderm Derivation From Pluripotent Stem Cells. J Cell Physiol. 2016;231(9):1994-2006. doi:10.1002/jcp.25308</mixed-citation><mixed-citation xml:lang="ru">74.	Viotti M, Nowotschin S, Hadjantonakis AK. SOX17 links gut endoderm morphogenesis and germ layer segregation. Nat Cell Biol. 2014;16(12):1146-1156. doi:10.1038/ncb3070</mixed-citation></citation-alternatives></ref><ref id="B75"><label>75.</label><citation-alternatives><mixed-citation xml:lang="en">75.	Kaufman-Francis K, Goh HN, Kojima Y, et al. Differential response of epiblast stem cells to Nodal and Activin signalling: a paradigm of early endoderm development in the embryo. Philos Trans R Soc Lond B Biol Sci. 2014;369(1657):20130550. doi:10.1098/rstb.2013.0550</mixed-citation><mixed-citation xml:lang="ru">75.	Dixit R, Ai X, Fine A. Derivation of lung mesenchymal lineages from the fetal mesothelium requires hedgehog signaling for mesothelial cell entry. Development. 2013;140(21):4398-4406. doi:10.1242/dev.098079</mixed-citation></citation-alternatives></ref><ref id="B76"><label>76.</label><citation-alternatives><mixed-citation xml:lang="en">76.	Li L, Song L, Liu C, et al. Ectodermal progenitors derived from epiblast stem cells by inhibition of Nodal signaling. J Mol Cell Biol. 2015;7(5):455-465. doi:10.1093/jmcb/mjv030</mixed-citation><mixed-citation xml:lang="ru">76.	Mohammadnia A, Yaqubi M, Pourasgari F, et al. Signaling and Gene Regulatory Networks Governing Definitive Endoderm Derivation From Pluripotent Stem Cells. J Cell Physiol. 2016;231(9):1994-2006. doi:10.1002/jcp.25308</mixed-citation></citation-alternatives></ref><ref id="B77"><label>77.</label><citation-alternatives><mixed-citation xml:lang="en">77.	Rangarajan A, Talora C, Okuyama R, et al. Notch signaling is a direct determinant of keratinocyte growth arrest and entry into differentiation. EMBO J. 2001;20(13):3427-3436. doi:10.1093/emboj/20.13.3427</mixed-citation><mixed-citation xml:lang="ru">77.	Kaufman-Francis K, Goh HN, Kojima Y, et al. Differential response of epiblast stem cells to Nodal and Activin signalling: a paradigm of early endoderm development in the embryo. Philos Trans R Soc Lond B Biol Sci. 2014;369(1657):20130550. doi:10.1098/rstb.2013.0550</mixed-citation></citation-alternatives></ref><ref id="B78"><label>78.</label><citation-alternatives><mixed-citation xml:lang="en">78.	Meng X, Qiu L, Song H, Dang N. MAPK Pathway Involved in Epidermal Terminal Differentiation of Normal Human Epidermal Keratinocytes. Open Med (Wars). 2018;13:189-195. doi:10.1515/med-2018-0029</mixed-citation><mixed-citation xml:lang="ru">78.	Li L, Song L, Liu C, et al. Ectodermal progenitors derived from epiblast stem cells by inhibition of Nodal signaling. J Mol Cell Biol. 2015;7(5):455-465. doi:10.1093/jmcb/mjv030</mixed-citation></citation-alternatives></ref><ref id="B79"><label>79.</label><citation-alternatives><mixed-citation xml:lang="en">79.	Bikle DD, Xie Z, Tu CL. Calcium regulation of keratinocyte differentiation. Expert Rev Endocrinol Metab. 2012;7(4):461-472. doi:10.1586/eem.12.34</mixed-citation><mixed-citation xml:lang="ru">79.	Rangarajan A, Talora C, Okuyama R, et al. Notch signaling is a direct determinant of keratinocyte growth arrest and entry into differentiation. EMBO J. 2001;20(13):3427-3436. doi:10.1093/emboj/20.13.3427</mixed-citation></citation-alternatives></ref><ref id="B80"><label>80.</label><citation-alternatives><mixed-citation xml:lang="en">80.	Gadue P, Huber TL, Paddison PJ, Keller GM. Wnt and TGF-beta signaling are required for the induction of an in vitro model of primitive streak formation using embryonic stem cells. Proc Natl Acad Sci U S A. 2006;103(45):16806-16811. doi:10.1073/pnas.0603916103</mixed-citation><mixed-citation xml:lang="ru">80.	Meng X, Qiu L, Song H, Dang N. MAPK Pathway Involved in Epidermal Terminal Differentiation of Normal Human Epidermal Keratinocytes. Open Med (Wars). 2018;13:189-195. doi:10.1515/med-2018-0029</mixed-citation></citation-alternatives></ref><ref id="B81"><label>81.</label><citation-alternatives><mixed-citation xml:lang="en">81.	Liu C, Peng G, Jing N. TGF-β signaling pathway in early mouse development and embryonic stem cells. Acta Biochim Biophys Sin (Shanghai). 2018;50(1):68-73. doi:10.1093/abbs/gmx120</mixed-citation><mixed-citation xml:lang="ru">81.	Bikle DD, Xie Z, Tu CL. Calcium regulation of keratinocyte differentiation. Expert Rev Endocrinol Metab. 2012;7(4):461-472. doi:10.1586/eem.12.34</mixed-citation></citation-alternatives></ref><ref id="B82"><label>82.</label><citation-alternatives><mixed-citation xml:lang="en">82.	El Kholtei J, Codina-Tobias M, Schier AF. Nodal Signaling: A Paradigm for TGFβ Signaling in Embryonic Development. Annu Rev Cell Dev Biol. 2025;41(1):45-88. doi:10.1146/annurev-cellbio-112122-030209 EDN: ZQYFEX</mixed-citation><mixed-citation xml:lang="ru">82.	Gadue P, Huber TL, Paddison PJ, Keller GM. Wnt and TGF-beta signaling are required for the induction of an in vitro model of primitive streak formation using embryonic stem cells. Proc Natl Acad Sci U S A. 2006;103(45):16806-16811. doi:10.1073/pnas.0603916103</mixed-citation></citation-alternatives></ref><ref id="B83"><label>83.</label><citation-alternatives><mixed-citation xml:lang="en">83.	Hernández-Martínez R, Nowotschin S, Harland LTG, et al. Axin1 and Axin2 regulate the WNT-signaling landscape to promote distinct mesoderm programs. Preprint. bioRxiv. 2024;2024.09.11.612342. doi:10.1101/2024.09.11.612342</mixed-citation><mixed-citation xml:lang="ru">83.	Liu C, Peng G, Jing N. TGF-β signaling pathway in early mouse development and embryonic stem cells. Acta Biochim Biophys Sin (Shanghai). 2018;50(1):68-73. doi:10.1093/abbs/gmx120</mixed-citation></citation-alternatives></ref><ref id="B84"><label>84.</label><citation-alternatives><mixed-citation xml:lang="en">84.	Price FD, Yin H, Jones A, et al. Canonical Wnt signaling induces a primitive endoderm metastable state in mouse embryonic stem cells. Stem Cells. 2013;31(4):752-764. doi:10.1002/stem.1321</mixed-citation><mixed-citation xml:lang="ru">84.	El Kholtei J, Codina-Tobias M, Schier AF. Nodal Signaling: A Paradigm for TGFβ Signaling in Embryonic Development. Annu Rev Cell Dev Biol. 2025;41(1):45-88. doi:10.1146/annurev-cellbio-112122-030209 EDN: ZQYFEX</mixed-citation></citation-alternatives></ref><ref id="B85"><label>85.</label><citation-alternatives><mixed-citation xml:lang="en">85.	Johansson BM, Wiles MV. Evidence for involvement of activin A and bone morphogenetic protein 4 in mammalian mesoderm and hematopoietic development. Mol Cell Biol. 1995;15(1):141-151. doi:10.1128/MCB.15.1.141</mixed-citation><mixed-citation xml:lang="ru">85.	Hernández-Martínez R, Nowotschin S, Harland LTG, et al. Axin1 and Axin2 regulate the WNT-signaling landscape to promote distinct mesoderm programs. Preprint. bioRxiv. 2024;2024.09.11.612342. doi:10.1101/2024.09.11.612342</mixed-citation></citation-alternatives></ref><ref id="B86"><label>86.</label><citation-alternatives><mixed-citation xml:lang="en">86.	Kuijk EW, van Tol LT, Van de Velde H, et al. The roles of FGF and MAP kinase signaling in the segregation of the epiblast and hypoblast cell lineages in bovine and human embryos. Development. 2012;139(5):871-882. doi:10.1242/dev.071688</mixed-citation><mixed-citation xml:lang="ru">86.	Price FD, Yin H, Jones A, et al. Canonical Wnt signaling induces a primitive endoderm metastable state in mouse embryonic stem cells. Stem Cells. 2013;31(4):752-764. doi:10.1002/stem.1321</mixed-citation></citation-alternatives></ref><ref id="B87"><label>87.</label><citation-alternatives><mixed-citation xml:lang="en">87.	Athanasouli P, Vanhessche T, Lluis F. Divergent destinies: insights into the molecular mechanisms underlying EPI and PE fate determination. Life Sci Alliance. 2025;8(3):e202403091. doi:10.26508/lsa.202403091 EDN: RYOJNL</mixed-citation><mixed-citation xml:lang="ru">87.	Johansson BM, Wiles MV. Evidence for involvement of activin A and bone morphogenetic protein 4 in mammalian mesoderm and hematopoietic development. Mol Cell Biol. 1995;15(1):141-151. doi:10.1128/MCB.15.1.141</mixed-citation></citation-alternatives></ref><ref id="B88"><label>88.</label><citation-alternatives><mixed-citation xml:lang="en">88.	Liu C, Peng G, Jing N. TGF-β signaling pathway in early mouse development and embryonic stem cells. Acta Biochim Biophys Sin (Shanghai). 2018;50(1):68-73. doi:10.1093/abbs/gmx120</mixed-citation><mixed-citation xml:lang="ru">88.	Kuijk EW, van Tol LT, Van de Velde H, et al. The roles of FGF and MAP kinase signaling in the segregation of the epiblast and hypoblast cell lineages in bovine and human embryos. Development. 2012;139(5):871-882. doi:10.1242/dev.071688</mixed-citation></citation-alternatives></ref><ref id="B89"><label>89.</label><citation-alternatives><mixed-citation xml:lang="en">89.	Ferrer-Vaquer A, Viotti M, Hadjantonakis AK. Transitions between epithelial and mesenchymal states and the morphogenesis of the early mouse embryo. Cell Adh Migr. 2010;4(3):447-457. doi:10.4161/cam.4.3.10771</mixed-citation><mixed-citation xml:lang="ru">89.	Athanasouli P, Vanhessche T, Lluis F. Divergent destinies: insights into the molecular mechanisms underlying EPI and PE fate determination. Life Sci Alliance. 2025;8(3):e202403091. doi:10.26508/lsa.202403091 EDN: RYOJNL</mixed-citation></citation-alternatives></ref><ref id="B90"><label>90.</label><citation-alternatives><mixed-citation xml:lang="en">90.	Frum T, Regulation of cell fate by the stem cell factors Cdx2, Oct4 and Sox2 in the early mouse embryo, UC Santa Cruz, 2014, ProQuest ID: Frum_ucsc_0036E_10614. Merritt ID: ark:/13030/m56t21tf. Retrieved from https://escholarship.org/uc/item/0k16d6b4/</mixed-citation><mixed-citation xml:lang="ru">90.	Liu C, Peng G, Jing N. TGF-β signaling pathway in early mouse development and embryonic stem cells. Acta Biochim Biophys Sin (Shanghai). 2018;50(1):68-73. doi:10.1093/abbs/gmx120</mixed-citation></citation-alternatives></ref><ref id="B91"><label>91.</label><citation-alternatives><mixed-citation xml:lang="en">91.	Simmet K, Klymiuk N, Zakhartchenko V, et al. 62 bovine OCT4 (POU5F1) knockout embryos fail during the second lineage differentiation due to loss of NANOG. Rep Fert Development. 2016; 29: 138. doi:10.1071/Rdv29n1Ab62</mixed-citation><mixed-citation xml:lang="ru">91.	Ferrer-Vaquer A, Viotti M, Hadjantonakis AK. Transitions between epithelial and mesenchymal states and the morphogenesis of the early mouse embryo. Cell Adh Migr. 2010;4(3):447-457. doi:10.4161/cam.4.3.10771</mixed-citation></citation-alternatives></ref><ref id="B92"><label>92.</label><citation-alternatives><mixed-citation xml:lang="en">92.	Azami T, Waku T, Matsumoto K, et al. Klf5 maintains the balance of primitive endoderm versus epiblast specification during mouse embryonic development by suppression of Fgf4. Development. 2017;144(20):3706-3718. doi:10.1242/dev.150755</mixed-citation><mixed-citation xml:lang="ru">92.	Frum T, Regulation of cell fate by the stem cell factors Cdx2, Oct4 and Sox2 in the early mouse embryo, UC Santa Cruz, 2014, ProQuest ID: Frum_ucsc_0036E_10614. Merritt ID: ark:/13030/m56t21tf. Retrieved from https://escholarship.org/uc/item/0k16d6b4/</mixed-citation></citation-alternatives></ref><ref id="B93"><label>93.</label><citation-alternatives><mixed-citation xml:lang="en">93.	Sierra RA, Hoverter NP, Ramirez RN, et al. TCF7L1 suppresses primitive streak gene expression to support human embryonic stem cell pluripotency. Development. 2018;145(4):dev161075. doi:10.1242/dev.161075</mixed-citation><mixed-citation xml:lang="ru">93.	Simmet K, Klymiuk N, Zakhartchenko V, et al. 62 bovine OCT4 (POU5F1) knockout embryos fail during the second lineage differentiation due to loss of NANOG. Rep Fert Development. 2016; 29: 138. doi:10.1071/Rdv29n1Ab62</mixed-citation></citation-alternatives></ref><ref id="B94"><label>94.</label><citation-alternatives><mixed-citation xml:lang="en">94.	Paik DT, Tian L, Williams IM, et al. Single-Cell RNA Sequencing Unveils Unique Transcriptomic Signatures of Organ-Specific Endothelial Cells. Circulation. 2020;142(19):1848-1862. doi:10.1161/CIRCULATIONAHA.119.041433 EDN: WBSHQJ</mixed-citation><mixed-citation xml:lang="ru">94.	Azami T, Waku T, Matsumoto K, et al. Klf5 maintains the balance of primitive endoderm versus epiblast specification during mouse embryonic development by suppression of Fgf4. Development. 2017;144(20):3706-3718. doi:10.1242/dev.150755</mixed-citation></citation-alternatives></ref><ref id="B95"><label>95.</label><citation-alternatives><mixed-citation xml:lang="en">95.	Schupp JC, Adams TS, Cosme C Jr, et al. Integrated Single-Cell Atlas of Endothelial Cells of the Human Lung. Circulation. 2021;144(4):286-302. doi:10.1161/CIRCULATIONAHA.120.052318 EDN: HFSUPT</mixed-citation><mixed-citation xml:lang="ru">95.	Sierra RA, Hoverter NP, Ramirez RN, et al. TCF7L1 suppresses primitive streak gene expression to support human embryonic stem cell pluripotency. Development. 2018;145(4):dev161075. doi:10.1242/dev.161075</mixed-citation></citation-alternatives></ref><ref id="B96"><label>96.</label><citation-alternatives><mixed-citation xml:lang="en">96.	Trimm E, Red-Horse K. Vascular endothelial cell development and diversity. Nat Rev Cardiol. 2023;20(3):197-210. doi:10.1038/s41569-022-00770-1 EDN: GFSOTW</mixed-citation><mixed-citation xml:lang="ru">96.	Paik DT, Tian L, Williams IM, et al. Single-Cell RNA Sequencing Unveils Unique Transcriptomic Signatures of Organ-Specific Endothelial Cells. Circulation. 2020;142(19):1848-1862. doi:10.1161/CIRCULATIONAHA.119.041433 EDN: WBSHQJ</mixed-citation></citation-alternatives></ref><ref id="B97"><label>97.</label><citation-alternatives><mixed-citation xml:lang="en">97.	Web resource proteinatlas.org accompanied by article Uhlén M, Fagerberg L, Hallström BM, et al. Proteomics. Tissue-based map of the human proteome. Science. 2015;347(6220):1260419. doi:10.1126/science.1260419 EDN: WXXTZC</mixed-citation><mixed-citation xml:lang="ru">97.	Schupp JC, Adams TS, Cosme C Jr, et al. Integrated Single-Cell Atlas of Endothelial Cells of the Human Lung. Circulation. 2021;144(4):286-302. doi:10.1161/CIRCULATIONAHA.120.052318 EDN: HFSUPT</mixed-citation></citation-alternatives></ref><ref id="B98"><label>98.</label><citation-alternatives><mixed-citation xml:lang="en">98.	Deev RV, Slepov YuK, Indeikin FA. Metaplasia as an epigenetic problem of variant and deviant differentiation. In: Innovative technologies for studying histogenesis, reactivity, and tissue regeneration. Proceedings of the Military Medical Academy. Vol. 263. / edited by R.G. Makiyev and I.A. Odintsova. - St. Petersburg: Military Medical Academy, 2024. - 148-156 EDN: BXGGTL</mixed-citation><mixed-citation xml:lang="ru">98.	Trimm E, Red-Horse K. Vascular endothelial cell development and diversity. Nat Rev Cardiol. 2023;20(3):197-210. doi:10.1038/s41569-022-00770-1 EDN: GFSOTW</mixed-citation></citation-alternatives></ref><ref id="B99"><label>99.</label><citation-alternatives><mixed-citation xml:lang="en">99.	Chumduri C, Gurumurthy RK, Berger H, et al. Opposing Wnt signals regulate cervical squamocolumnar homeostasis and emergence of metaplasia. Nat Cell Biol. 2021;23(2):184-197. doi:10.1038/s41556-020-00619-0 EDN: HMXMDZ</mixed-citation><mixed-citation xml:lang="ru">99.	Web resource proteinatlas.org accompanied by article Uhlén M, Fagerberg L, Hallström BM, et al. Proteomics. Tissue-based map of the human proteome. Science. 2015;347(6220):1260419. doi:10.1126/science.1260419 EDN: WXXTZC</mixed-citation></citation-alternatives></ref><ref id="B100"><label>100.</label><citation-alternatives><mixed-citation xml:lang="en">100.	Kathiriya JJ, Wang C, Zhou M, et al. Human alveolar type 2 epithelium transdifferentiates into metaplastic KRT5+ basal cells. Nat Cell Biol. 2022;24(1):10-23. doi:10.1038/s41556-021-00809-4 EDN: WMWIMA</mixed-citation><mixed-citation xml:lang="ru">100.	Деев РВ, Слепов ЮК, Индейкин ФА. Метаплазия как эпигенетическая проблема вариантной и девиантной дифференцировки. В кн.: Инновационные технологии изучения гистогенеза, реактивности и регенерации тканей. Труды Военно-медицинской академии. Т. 263. / под ред. Р.Г. Макиева и И.А. Одинцовой. – СПб.: ВМедА, 2024. – 148-156 EDN: BXGGTL</mixed-citation></citation-alternatives></ref><ref id="B101"><label>101.</label><citation-alternatives><mixed-citation xml:lang="en">101.	Rodrigues JP, David L, Almeida R, et al. Mechanisms of regulation of normal and metaplastic intestinal differentiation. Histol Histopathol. 2018;33(6):523-532. doi:10.14670/hh-11-938</mixed-citation><mixed-citation xml:lang="ru">101.	Chumduri C, Gurumurthy RK, Berger H, et al. Opposing Wnt signals regulate cervical squamocolumnar homeostasis and emergence of metaplasia. Nat Cell Biol. 2021;23(2):184-197. doi:10.1038/s41556-020-00619-0 EDN: HMXMDZ</mixed-citation></citation-alternatives></ref><ref id="B102"><label>102.</label><citation-alternatives><mixed-citation xml:lang="en">102.	Sun X, Gulyás M, Hjerpe A. Mesothelial differentiation as reflected by differential gene expression. Am J Respir Cell Mol Biol. 2004;30(4):510-518. doi:10.1165/rcmb.2003-0266OC</mixed-citation><mixed-citation xml:lang="ru">102.	Kathiriya JJ, Wang C, Zhou M, et al. Human alveolar type 2 epithelium transdifferentiates into metaplastic KRT5+ basal cells. Nat Cell Biol. 2022;24(1):10-23. doi:10.1038/s41556-021-00809-4 EDN: WMWIMA</mixed-citation></citation-alternatives></ref><ref id="B103"><label>103.</label><citation-alternatives><mixed-citation xml:lang="en">103. Chung-Welch N, Patton WF, Yen-Patton GP, et al. Phenotypic comparison between mesothelial and microvascular endothelial cell lineages using conventional endothelial cell markers, cytoskeletal protein markers and in vitro assays of angiogenic potential. Differentiation. 1989;42(1):44-53. doi:10.1111/j.1432-0436.1989.tb00606.x</mixed-citation><mixed-citation xml:lang="ru">103.	Rodrigues JP, David L, Almeida R, et al. Mechanisms of regulation of normal and metaplastic intestinal differentiation. Histol Histopathol. 2018;33(6):523-532. doi:10.14670/hh-11-938</mixed-citation></citation-alternatives></ref><ref id="B104"><label>104.</label><citation-alternatives><mixed-citation xml:lang="en">104. Zeisberg EM, Potenta S, Xie L, et al. Discovery of endothelial to mesenchymal transition as a source for carcinoma-associated fibroblasts. Cancer Res. 2007;67(21):10123-10128. doi:10.1158/0008-5472.CAN-07-3127</mixed-citation><mixed-citation xml:lang="ru">104.	Sun X, Gulyás M, Hjerpe A. Mesothelial differentiation as reflected by differential gene expression. Am J Respir Cell Mol Biol. 2004;30(4):510-518. doi:10.1165/rcmb.2003-0266OC</mixed-citation></citation-alternatives></ref><ref id="B105"><label>105.</label><citation-alternatives><mixed-citation xml:lang="en">105. Li Y, Lui KO, Zhou B. Reassessing endothelial-to-mesenchymal transition in cardiovascular diseases. Nat Rev Cardiol. 2018;15(8):445-456. doi:10.1038/s41569-018-0023-y</mixed-citation><mixed-citation xml:lang="ru">105. Chung-Welch N, Patton WF, Yen-Patton GP, et al. Phenotypic comparison between mesothelial and microvascular endothelial cell lineages using conventional endothelial cell markers, cytoskeletal protein markers and in vitro assays of angiogenic potential. Differentiation. 1989;42(1):44-53. doi:10.1111/j.1432-0436.1989.tb00606.x</mixed-citation></citation-alternatives></ref><ref id="B106"><label>106.</label><citation-alternatives><mixed-citation xml:lang="en">106. Hu Q, Zhang T, Li Y, et al. β2AR-dependent signaling contributes to in-vivo reendothelialization capacity of endothelial progenitor cells by shear stress. J Hypertens. 2020;38(1):82-94. doi:10.1097/HJH.0000000000002203 EDN: YNUEWI</mixed-citation><mixed-citation xml:lang="ru">106. Zeisberg EM, Potenta S, Xie L, et al. Discovery of endothelial to mesenchymal transition as a source for carcinoma-associated fibroblasts. Cancer Res. 2007;67(21):10123-10128. doi:10.1158/0008-5472.CAN-07-3127</mixed-citation></citation-alternatives></ref><ref id="B107"><label>107.</label><citation-alternatives><mixed-citation xml:lang="en">107. Yasui Y, Hart DA, Sugita N, et al. Time-Dependent Recovery of Human Synovial Membrane Mesenchymal Stem Cell Function After High-Dose Steroid Therapy: Case Report and Laboratory Study. Am J Sports Med. 2018;46(3):695-701. doi:10.1177/0363546517741307</mixed-citation><mixed-citation xml:lang="ru">107. Li Y, Lui KO, Zhou B. Reassessing endothelial-to-mesenchymal transition in cardiovascular diseases. Nat Rev Cardiol. 2018;15(8):445-456. doi:10.1038/s41569-018-0023-y</mixed-citation></citation-alternatives></ref><ref id="B108"><label>108.</label><citation-alternatives><mixed-citation xml:lang="en">108.	Hu J, Zhang E, Wu J, et al. Pressure shift mediated anoikis of endothelial cells in the flow field in vitro. Journal of Biomedical Science and Engineering, 2010;3:206-212. doi:10.4236/jbise.2010.32027</mixed-citation><mixed-citation xml:lang="ru">108. Hu Q, Zhang T, Li Y, et al. β2AR-dependent signaling contributes to in-vivo reendothelialization capacity of endothelial progenitor cells by shear stress. J Hypertens. 2020;38(1):82-94. doi:10.1097/HJH.0000000000002203 EDN: YNUEWI</mixed-citation></citation-alternatives></ref><ref id="B109"><label>109.</label><citation-alternatives><mixed-citation xml:lang="en">109.	Blanpain C, Fuchs E. Epidermal stem cells of the skin. Annu Rev Cell Dev Biol. 2006;22:339-373. doi:10.1146/annurev.cellbio.22.010305.104357</mixed-citation><mixed-citation xml:lang="ru">109. Yasui Y, Hart DA, Sugita N, et al. Time-Dependent Recovery of Human Synovial Membrane Mesenchymal Stem Cell Function After High-Dose Steroid Therapy: Case Report and Laboratory Study. Am J Sports Med. 2018;46(3):695-701. doi:10.1177/0363546517741307</mixed-citation></citation-alternatives></ref><ref id="B110"><label>110.</label><citation-alternatives><mixed-citation xml:lang="en">110.	Yanger K, Knigin D, Zong Y, et al. Adult hepatocytes are generated by self-duplication rather than stem cell differentiation. Cell Stem Cell. 2014;15(3):340-349. doi:10.1016/j.stem.2014.06.003 EDN: YBUZQY</mixed-citation><mixed-citation xml:lang="ru">110.	Hu J, Zhang E, Wu J, et al. Pressure shift mediated anoikis of endothelial cells in the flow field in vitro. Journal of Biomedical Science and Engineering, 2010;3:206-212. doi:10.4236/jbise.2010.32027</mixed-citation></citation-alternatives></ref><ref id="B111"><label>111.</label><citation-alternatives><mixed-citation xml:lang="en">111.	Mutsaers SE, Prêle CM, Lansley SM, Herrick SE. The origin of regenerating mesothelium: a historical perspective. Int J Artif Organs. 2007;30(6):484-494. doi:10.1177/039139880703000606 EDN: XTZTBK</mixed-citation><mixed-citation xml:lang="ru">111.	Blanpain C, Fuchs E. Epidermal stem cells of the skin. Annu Rev Cell Dev Biol. 2006;22:339-373. doi:10.1146/annurev.cellbio.22.010305.104357</mixed-citation></citation-alternatives></ref><ref id="B112"><label>112.</label><citation-alternatives><mixed-citation xml:lang="en">112.	Andrianova NV, Buyan MI, Zorova LD, et al. Kidney Cells Regeneration: Dedifferentiation of Tubular Epithelium, Resident Stem Cells and Possible Niches for Renal Progenitors. Int J Mol Sci. 2019;20(24):6326. doi:10.3390/ijms20246326 EDN: FTGSTP</mixed-citation><mixed-citation xml:lang="ru">112.	Yanger K, Knigin D, Zong Y, et al. Adult hepatocytes are generated by self-duplication rather than stem cell differentiation. Cell Stem Cell. 2014;15(3):340-349. doi:10.1016/j.stem.2014.06.003 EDN: YBUZQY</mixed-citation></citation-alternatives></ref><ref id="B113"><label>113.</label><citation-alternatives><mixed-citation xml:lang="en">113.	Ricard N, Bailly S, Guignabert C, Simons M. The quiescent endothelium: signalling pathways regulating organ-specific endothelial normalcy. Nat Rev Cardiol. 2021;18(8):565-580. doi:10.1038/s41569-021-00517-4 EDN: UCINSI</mixed-citation><mixed-citation xml:lang="ru">113.	Mutsaers SE, Prêle CM, Lansley SM, Herrick SE. The origin of regenerating mesothelium: a historical perspective. Int J Artif Organs. 2007;30(6):484-494. doi:10.1177/039139880703000606 EDN: XTZTBK</mixed-citation></citation-alternatives></ref><ref id="B114"><label>114.</label><citation-alternatives><mixed-citation xml:lang="en">114.	Asahara T, Masuda H, Takahashi T, et al. Bone marrow origin of endothelial progenitor cells responsible for postnatal vasculogenesis in physiological and pathological neovascularization. Circ Res. 1999;85(3):221-228. doi:10.1161/01.res.85.3.221</mixed-citation><mixed-citation xml:lang="ru">114.	Andrianova NV, Buyan MI, Zorova LD, et al. Kidney Cells Regeneration: Dedifferentiation of Tubular Epithelium, Resident Stem Cells and Possible Niches for Renal Progenitors. Int J Mol Sci. 2019;20(24):6326. doi:10.3390/ijms20246326 EDN: FTGSTP</mixed-citation></citation-alternatives></ref><ref id="B115"><label>115.</label><citation-alternatives><mixed-citation xml:lang="en">115.	Web resource ProteinAtlas accesses in year 2025 https://www.proteinatlas.org/search/cell_type_group_category_rna%3AApical+squamous+epithelial+cells%2CSuprabasal+cells%3BCell+type+enriched accompanied by article Uhlén M, Fagerberg L, Hallström BM, et al. Proteomics. Tissue-based map of the human proteome. Science. 2015;347(6220):1260419. doi:10.1126/science.1260419</mixed-citation><mixed-citation xml:lang="ru">115.	Ricard N, Bailly S, Guignabert C, Simons M. The quiescent endothelium: signalling pathways regulating organ-specific endothelial normalcy. Nat Rev Cardiol. 2021;18(8):565-580. doi:10.1038/s41569-021-00517-4 EDN: UCINSI</mixed-citation></citation-alternatives></ref><ref id="B116"><label>116.</label><citation-alternatives><mixed-citation xml:lang="en">116.	Web resource ProteinAtlas accesses in year 2025 https://www.proteinatlas.org/search/ce_enriched%3Acolon%3BColon+enterocytes%3BVery+high accompanied by article Uhlén M, Fagerberg L, Hallström BM, et al. Proteomics. Tissue-based map of the human proteome. Science. 2015;347(6220):1260419. doi:10.1126/science.1260419</mixed-citation><mixed-citation xml:lang="ru">116.	Asahara T, Masuda H, Takahashi T, et al. Bone marrow origin of endothelial progenitor cells responsible for postnatal vasculogenesis in physiological and pathological neovascularization. Circ Res. 1999;85(3):221-228. doi:10.1161/01.res.85.3.221</mixed-citation></citation-alternatives></ref><ref id="B117"><label>117.</label><citation-alternatives><mixed-citation xml:lang="en">117.	Web resource ProteinAtlas accesses in year 2025 https://www.proteinatlas.org/search/ce_enriched%3Astomach%3BParietal+cells%3BVery+high accompanied by article Uhlén M, Fagerberg L, Hallström BM, et al. Proteomics. Tissue-based map of the human proteome. Science. 2015;347(6220):1260419. doi:10.1126/science.1260419</mixed-citation><mixed-citation xml:lang="ru">117.	Web resource ProteinAtlas accesses in year 2025 https://www.proteinatlas.org/search/cell_type_group_category_rna%3AApical+squamous+epithelial+cells%2CSuprabasal+cells%3BCell+type+enriched accompanied by article Uhlén M, Fagerberg L, Hallström BM, et al. Proteomics. Tissue-based map of the human proteome. Science. 2015;347(6220):1260419. doi:10.1126/science.1260419</mixed-citation></citation-alternatives></ref><ref id="B118"><label>118.</label><citation-alternatives><mixed-citation xml:lang="en">118.	Web resource ProteinAtlas accesses in year 2025 https://www.proteinatlas.org/search/ce_enriched%3Astomach%3BChief+cells%3BVery+high accompanied by article Uhlén M, Fagerberg L, Hallström BM, et al. Proteomics. Tissue-based map of the human proteome. Science. 2015;347(6220):1260419. doi:10.1126/science.1260419</mixed-citation><mixed-citation xml:lang="ru">118.	Web resource ProteinAtlas accesses in year 2025 https://www.proteinatlas.org/search/ce_enriched%3Acolon%3BColon+enterocytes%3BVery+high accompanied by article Uhlén M, Fagerberg L, Hallström BM, et al. Proteomics. Tissue-based map of the human proteome. Science. 2015;347(6220):1260419. doi:10.1126/science.1260419</mixed-citation></citation-alternatives></ref><ref id="B119"><label>119.</label><citation-alternatives><mixed-citation xml:lang="en">119.	Web resource ProteinAtlas accesses in year 2025 https://www.proteinatlas.org/search/ce_enriched%3Astomach%3BGastric+mucous+cells%3BVery+high accompanied by article Uhlén M, Fagerberg L, Hallström BM, et al. Proteomics. Tissue-based map of the human proteome. Science. 2015;347(6220):1260419. doi:10.1126/science.1260419</mixed-citation><mixed-citation xml:lang="ru">119.	Web resource ProteinAtlas accesses in year 2025 https://www.proteinatlas.org/search/ce_enriched%3Astomach%3BParietal+cells%3BVery+high accompanied by article Uhlén M, Fagerberg L, Hallström BM, et al. Proteomics. Tissue-based map of the human proteome. Science. 2015;347(6220):1260419. doi:10.1126/science.1260419</mixed-citation></citation-alternatives></ref><ref id="B120"><label>120.</label><citation-alternatives><mixed-citation xml:lang="en">120.	Web resource ProteinAtlas accesses in year 2025 https://www.proteinatlas.org/search/cell_type_category_rna%3APodocytes%2CProximal+tubule+cells%2CLoop+of+henle+epithelial+cells%2CPapillary+tip+epithelial+cells%2CDistal+convoluted+tubule+cells%3BCell+type+enriched+AND+show_columns%3Atissuespecificity+AND+sort_by%3Atissue+specific+score accompanied by article Uhlén M, Fagerberg L, Hallström BM, et al. Proteomics. Tissue-based map of the human proteome. Science. 2015;347(6220):1260419. doi:10.1126/science.1260419</mixed-citation><mixed-citation xml:lang="ru">120.	Web resource ProteinAtlas accesses in year 2025 https://www.proteinatlas.org/search/ce_enriched%3Astomach%3BChief+cells%3BVery+high accompanied by article Uhlén M, Fagerberg L, Hallström BM, et al. Proteomics. Tissue-based map of the human proteome. Science. 2015;347(6220):1260419. doi:10.1126/science.1260419</mixed-citation></citation-alternatives></ref><ref id="B121"><label>121.</label><citation-alternatives><mixed-citation xml:lang="en">121.	Web resource ProteinAtlas accesses in year 2025 https://www.proteinatlas.org/search/cell_type_category_rna%3AVascular+endothelial+cells%2CLymphatic+endothelial+cells%3BCell+type+enriched+AND+show_columns%3Atissuespecificity+AND+sort_by%3Atissue+specific+score accompanied by article Uhlén M, Fagerberg L, Hallström BM, et al. Proteomics. Tissue-based map of the human proteome. Science. 2015;347(6220):1260419. doi:10.1126/science.1260419</mixed-citation><mixed-citation xml:lang="ru">121.	Web resource ProteinAtlas accesses in year 2025 https://www.proteinatlas.org/search/ce_enriched%3Astomach%3BGastric+mucous+cells%3BVery+high accompanied by article Uhlén M, Fagerberg L, Hallström BM, et al. Proteomics. Tissue-based map of the human proteome. Science. 2015;347(6220):1260419. doi:10.1126/science.1260419</mixed-citation></citation-alternatives></ref><ref id="B122"><label>122.</label><citation-alternatives><mixed-citation xml:lang="en">122.	Moll R, Divo M, Langbein L. The human keratins: biology and pathology. Histochem Cell Biol. 2008;129(6):705-733. doi:10.1007/s00418-008-0435-6 EDN: XXBMNT</mixed-citation><mixed-citation xml:lang="ru">122.	Web resource ProteinAtlas accesses in year 2025 https://www.proteinatlas.org/search/cell_type_category_rna%3APodocytes%2CProximal+tubule+cells%2CLoop+of+henle+epithelial+cells%2CPapillary+tip+epithelial+cells%2CDistal+convoluted+tubule+cells%3BCell+type+enriched+AND+show_columns%3Atissuespecificity+AND+sort_by%3Atissue+specific+score accompanied by article Uhlén M, Fagerberg L, Hallström BM, et al. Proteomics. Tissue-based map of the human proteome. Science. 2015;347(6220):1260419. doi:10.1126/science.1260419</mixed-citation></citation-alternatives></ref><ref id="B123"><label>123.</label><citation-alternatives><mixed-citation xml:lang="en">123.	Rao KS, Babu KK, Gupta PD. Keratins and skin disorders. Cell Biol Int. 1996;20(4):261-274.</mixed-citation><mixed-citation xml:lang="ru">123.	Web resource ProteinAtlas accesses in year 2025 https://www.proteinatlas.org/search/cell_type_category_rna%3AVascular+endothelial+cells%2CLymphatic+endothelial+cells%3BCell+type+enriched+AND+show_columns%3Atissuespecificity+AND+sort_by%3Atissue+specific+score accompanied by article Uhlén M, Fagerberg L, Hallström BM, et al. Proteomics. Tissue-based map of the human proteome. Science. 2015;347(6220):1260419. doi:10.1126/science.1260419</mixed-citation></citation-alternatives></ref><ref id="B124"><label>124.</label><citation-alternatives><mixed-citation xml:lang="en">124.	Maupérin M, Sun Y, Glandorf T, et al. A feedback circuitry involving γ-actin, β-actin and nonmuscle myosin-2 A controls tight junction and apical cortex mechanics. Nat Commun. 2025;16(1):2514. doi:10.1038/s41467-025-57428-y EDN: AMSMNQ</mixed-citation><mixed-citation xml:lang="ru">124.	Moll R, Divo M, Langbein L. The human keratins: biology and pathology. Histochem Cell Biol. 2008;129(6):705-733. doi:10.1007/s00418-008-0435-6 EDN: XXBMNT</mixed-citation></citation-alternatives></ref><ref id="B125"><label>125.</label><citation-alternatives><mixed-citation xml:lang="en">125.	Hatzfeld M, Keil R, Magin TM. Desmosomes and Intermediate Filaments: Their Consequences for Tissue Mechanics. Cold Spring Harb Perspect Biol. 2017;9(6):a029157. doi:10.1101/cshperspect.a029157</mixed-citation><mixed-citation xml:lang="ru">125.	Rao KS, Babu KK, Gupta PD. Keratins and skin disorders. Cell Biol Int. 1996;20(4):261-274.</mixed-citation></citation-alternatives></ref><ref id="B126"><label>126.</label><citation-alternatives><mixed-citation xml:lang="en">126.	Winters NI, Bader DM. Development of the Serosal Mesothelium. J Dev Biol. 2013; 1(2):64-81. doi:10.3390/jdb1020064</mixed-citation><mixed-citation xml:lang="ru">126.	Maupérin M, Sun Y, Glandorf T, et al. A feedback circuitry involving γ-actin, β-actin and nonmuscle myosin-2 A controls tight junction and apical cortex mechanics. Nat Commun. 2025;16(1):2514. doi:10.1038/s41467-025-57428-y EDN: AMSMNQ</mixed-citation></citation-alternatives></ref><ref id="B127"><label>127.</label><citation-alternatives><mixed-citation xml:lang="en">127.	Baer PC, Bereiter-Hahn J, Schubert R, Geiger H. Differentiation status of human renal proximal and distal tubular epithelial cells in vitro: Differential expression of characteristic markers. Cells Tissues Organs. 2006;184(1):16-22. doi:10.1159/000096947</mixed-citation><mixed-citation xml:lang="ru">127.	Hatzfeld M, Keil R, Magin TM. Desmosomes and Intermediate Filaments: Their Consequences for Tissue Mechanics. Cold Spring Harb Perspect Biol. 2017;9(6):a029157. doi:10.1101/cshperspect.a029157</mixed-citation></citation-alternatives></ref><ref id="B128"><label>128.</label><citation-alternatives><mixed-citation xml:lang="en">128.	Franke WW, Schmid E, Osborn M, Weber K. Intermediate-sized filaments of human endothelial cells. J Cell Biol. 1979;81(3):570-580. doi:10.1083/jcb.81.3.570</mixed-citation><mixed-citation xml:lang="ru">128.	Winters NI, Bader DM. Development of the Serosal Mesothelium. J Dev Biol. 2013; 1(2):64-81. doi:10.3390/jdb1020064</mixed-citation></citation-alternatives></ref><ref id="B129"><label>129.</label><citation-alternatives><mixed-citation xml:lang="en">129.	Miettinen M, Fetsch JF. Distribution of keratins in normal endothelial cells and a spectrum of vascular tumors: implications in tumor diagnosis. Hum Pathol. 2000;31(9):1062-1067. doi:10.1053/hupa.2000.9843</mixed-citation><mixed-citation xml:lang="ru">129.	Baer PC, Bereiter-Hahn J, Schubert R, Geiger H. Differentiation status of human renal proximal and distal tubular epithelial cells in vitro: Differential expression of characteristic markers. Cells Tissues Organs. 2006;184(1):16-22. doi:10.1159/000096947</mixed-citation></citation-alternatives></ref><ref id="B130"><label>130.</label><citation-alternatives><mixed-citation xml:lang="en">130.	Prasain N, Stevens T. The actin cytoskeleton in endothelial cell phenotypes. Microvasc Res. 2009;77(1):53-63. doi:10.1016/j.mvr.2008.09.012 EDN: MIZGNF</mixed-citation><mixed-citation xml:lang="ru">130.	Franke WW, Schmid E, Osborn M, Weber K. Intermediate-sized filaments of human endothelial cells. J Cell Biol. 1979;81(3):570-580. doi:10.1083/jcb.81.3.570</mixed-citation></citation-alternatives></ref><ref id="B131"><label>131.</label><citation-alternatives><mixed-citation xml:lang="en">131.	Garcia-Hernandez V, Quiros M, Nusrat A. Intestinal epithelial claudins: expression and regulation in homeostasis and inflammation. Ann N Y Acad Sci. 2017;1397(1):66-79. doi:10.1111/nyas.13360 EDN: YGJXDG</mixed-citation><mixed-citation xml:lang="ru">131.	Miettinen M, Fetsch JF. Distribution of keratins in normal endothelial cells and a spectrum of vascular tumors: implications in tumor diagnosis. Hum Pathol. 2000;31(9):1062-1067. doi:10.1053/hupa.2000.9843</mixed-citation></citation-alternatives></ref><ref id="B132"><label>132.</label><citation-alternatives><mixed-citation xml:lang="en">132.	Mège RM, Ishiyama N. Integration of Cadherin Adhesion and Cytoskeleton at Adherens Junctions. Cold Spring Harb Perspect Biol. 2017;9(5):a028738. doi:10.1101/cshperspect.a028738</mixed-citation><mixed-citation xml:lang="ru">132.	Prasain N, Stevens T. The actin cytoskeleton in endothelial cell phenotypes. Microvasc Res. 2009;77(1):53-63. doi:10.1016/j.mvr.2008.09.012 EDN: MIZGNF</mixed-citation></citation-alternatives></ref><ref id="B133"><label>133.</label><citation-alternatives><mixed-citation xml:lang="en">133.	Kotini M, Barriga EH, Leslie J, et al. Gap junction protein Connexin-43 is a direct transcriptional regulator of N-cadherin in vivo. Nat Commun. 2018;9(1):3846. doi:10.1038/s41467-018-06368-x EDN: DMUDVU</mixed-citation><mixed-citation xml:lang="ru">133.	Garcia-Hernandez V, Quiros M, Nusrat A. Intestinal epithelial claudins: expression and regulation in homeostasis and inflammation. Ann N Y Acad Sci. 2017;1397(1):66-79. doi:10.1111/nyas.13360 EDN: YGJXDG</mixed-citation></citation-alternatives></ref><ref id="B134"><label>134.</label><citation-alternatives><mixed-citation xml:lang="en">134.	Retana C, Sanchez E, Perez-Lopez A, et al. Alterations of intercellular junctions in peritoneal mesothelial cells from patients undergoing dialysis: effect of retinoic Acid. Perit Dial Int. 2015;35(3):275-287. doi:10.3747/pdi.2012.00323 EDN: UTQVVH</mixed-citation><mixed-citation xml:lang="ru">134.	Mège RM, Ishiyama N. Integration of Cadherin Adhesion and Cytoskeleton at Adherens Junctions. Cold Spring Harb Perspect Biol. 2017;9(5):a028738. doi:10.1101/cshperspect.a028738</mixed-citation></citation-alternatives></ref><ref id="B135"><label>135.</label><citation-alternatives><mixed-citation xml:lang="en">135.	Markov AG, Amasheh S. Tight junction physiology of pleural mesothelium. Front Physiol. 2014;5:221. doi:10.3389/fphys.2014.00221 EDN: UEMCUB</mixed-citation><mixed-citation xml:lang="ru">135.	Kotini M, Barriga EH, Leslie J, et al. Gap junction protein Connexin-43 is a direct transcriptional regulator of N-cadherin in vivo. Nat Commun. 2018;9(1):3846. doi:10.1038/s41467-018-06368-x EDN: DMUDVU</mixed-citation></citation-alternatives></ref><ref id="B136"><label>136.</label><citation-alternatives><mixed-citation xml:lang="en">136.	Pelin K, Hirvonen A, Linnainmaa K. Expression of cell adhesion molecules and connexins in gap junctional intercellular communication deficient human mesothelioma tumour cell lines and communication competent primary mesothelial cells. Carcinogenesis. 1994;15(11):2673-2675. doi:10.1093/carcin/15.11.2673 EDN: IMTNBV</mixed-citation><mixed-citation xml:lang="ru">136.	Retana C, Sanchez E, Perez-Lopez A, et al. Alterations of intercellular junctions in peritoneal mesothelial cells from patients undergoing dialysis: effect of retinoic Acid. Perit Dial Int. 2015;35(3):275-287. doi:10.3747/pdi.2012.00323 EDN: UTQVVH</mixed-citation></citation-alternatives></ref><ref id="B137"><label>137.</label><citation-alternatives><mixed-citation xml:lang="en">137.	Zhuang W, Mitrou NGA, Kulak S, et al. Modulation of expression of Connexins 37, 40 and 43 in endothelial cells in culture. Front Netw Physiol. 2024;4:1199198. doi:10.3389/fnetp.2024.1199198 EDN: JSTSAH</mixed-citation><mixed-citation xml:lang="ru">137.	Markov AG, Amasheh S. Tight junction physiology of pleural mesothelium. Front Physiol. 2014;5:221. doi:10.3389/fphys.2014.00221 EDN: UEMCUB</mixed-citation></citation-alternatives></ref><ref id="B138"><label>138.</label><citation-alternatives><mixed-citation xml:lang="en">138.	Balkovetz DF, Chumley P, Amlal H. Downregulation of claudin-2 expression in renal epithelial cells by metabolic acidosis. Am J Physiol Renal Physiol. 2009;297(3):F604-F611. doi:10.1152/ajprenal.00043.2009</mixed-citation><mixed-citation xml:lang="ru">138.	Pelin K, Hirvonen A, Linnainmaa K. Expression of cell adhesion molecules and connexins in gap junctional intercellular communication deficient human mesothelioma tumour cell lines and communication competent primary mesothelial cells. Carcinogenesis. 1994;15(11):2673-2675. doi:10.1093/carcin/15.11.2673 EDN: IMTNBV</mixed-citation></citation-alternatives></ref><ref id="B139"><label>139.</label><citation-alternatives><mixed-citation xml:lang="en">139.	Hou J, Goodenough DA. Claudin-16 and claudin-19 function in the thick ascending limb. Curr Opin Nephrol Hypertens. 2010;19(5):483-488. doi:10.1097/MNH.0b013e32833b7125 EDN: NBDUED</mixed-citation><mixed-citation xml:lang="ru">139.	Zhuang W, Mitrou NGA, Kulak S, et al. Modulation of expression of Connexins 37, 40 and 43 in endothelial cells in culture. Front Netw Physiol. 2024;4:1199198. doi:10.3389/fnetp.2024.1199198 EDN: JSTSAH</mixed-citation></citation-alternatives></ref><ref id="B140"><label>140.</label><citation-alternatives><mixed-citation xml:lang="en">140.	Baer PC, Bereiter-Hahn J, Schubert R, Geiger H. Differentiation status of human renal proximal and distal tubular epithelial cells in vitro: Differential expression of characteristic markers. Cells Tissues Organs. 2006;184(1):16-22. doi:10.1159/000096947</mixed-citation><mixed-citation xml:lang="ru">140.	Balkovetz DF, Chumley P, Amlal H. Downregulation of claudin-2 expression in renal epithelial cells by metabolic acidosis. Am J Physiol Renal Physiol. 2009;297(3):F604-F611. doi:10.1152/ajprenal.00043.2009</mixed-citation></citation-alternatives></ref><ref id="B141"><label>141.</label><citation-alternatives><mixed-citation xml:lang="en">141.	Selim MS, Matani BR, Henry-Ojo HO, et al. Claudin 5 Across the Vascular Landscape: From Blood-Tissue Barrier Regulation to Disease Mechanisms. Cells. 2025;14(17):1346. doi:10.3390/cells14171346 EDN: SHGOQR</mixed-citation><mixed-citation xml:lang="ru">141.	Hou J, Goodenough DA. Claudin-16 and claudin-19 function in the thick ascending limb. Curr Opin Nephrol Hypertens. 2010;19(5):483-488. doi:10.1097/MNH.0b013e32833b7125 EDN: NBDUED</mixed-citation></citation-alternatives></ref><ref id="B142"><label>142.</label><citation-alternatives><mixed-citation xml:lang="en">142.	Vestweber D. VE-cadherin: the major endothelial adhesion molecule controlling cellular junctions and blood vessel formation. Arterioscler Thromb Vasc Biol. 2008;28(2):223-232. doi:10.1161/ATVBAHA.107.158014</mixed-citation><mixed-citation xml:lang="ru">142.	Baer PC, Bereiter-Hahn J, Schubert R, Geiger H. Differentiation status of human renal proximal and distal tubular epithelial cells in vitro: Differential expression of characteristic markers. Cells Tissues Organs. 2006;184(1):16-22. doi:10.1159/000096947</mixed-citation></citation-alternatives></ref><ref id="B143"><label>143.</label><citation-alternatives><mixed-citation xml:lang="en">143.	Muller WA, Weigl SA, Deng X, Phillips DM. PECAM-1 is required for transendothelial migration of leukocytes. J Exp Med. 1993;178(2):449-460. doi:10.1084/jem.178.2.449</mixed-citation><mixed-citation xml:lang="ru">143.	Selim MS, Matani BR, Henry-Ojo HO, et al. Claudin 5 Across the Vascular Landscape: From Blood-Tissue Barrier Regulation to Disease Mechanisms. Cells. 2025;14(17):1346. doi:10.3390/cells14171346 EDN: SHGOQR</mixed-citation></citation-alternatives></ref><ref id="B144"><label>144.</label><citation-alternatives><mixed-citation xml:lang="en">144.	Kim YS, Ho SB. Intestinal goblet cells and mucins in health and disease: recent insights and progress. Curr Gastroenterol Rep. 2010;12(5):319-330. doi:10.1007/s11894-010-0131-2 EDN: RSMNCJ</mixed-citation><mixed-citation xml:lang="ru">144.	Vestweber D. VE-cadherin: the major endothelial adhesion molecule controlling cellular junctions and blood vessel formation. Arterioscler Thromb Vasc Biol. 2008;28(2):223-232. doi:10.1161/ATVBAHA.107.158014</mixed-citation></citation-alternatives></ref><ref id="B145"><label>145.</label><citation-alternatives><mixed-citation xml:lang="en">145.	Matsui T, Amagai M. Dissecting the formation, structure and barrier function of the stratum corneum. Int Immunol. 2015;27(6):269-280. doi:10.1093/intimm/dxv013</mixed-citation><mixed-citation xml:lang="ru">145.	Muller WA, Weigl SA, Deng X, Phillips DM. PECAM-1 is required for transendothelial migration of leukocytes. J Exp Med. 1993;178(2):449-460. doi:10.1084/jem.178.2.449</mixed-citation></citation-alternatives></ref><ref id="B146"><label>146.</label><citation-alternatives><mixed-citation xml:lang="en">146.	Matsui T., Amagai, M. Erratum in Corrigendum, Int Immunol. 2017;29(5), 243-244. https://doi.org/10.1093/intimm/dxx024</mixed-citation><mixed-citation xml:lang="ru">146.	Kim YS, Ho SB. Intestinal goblet cells and mucins in health and disease: recent insights and progress. Curr Gastroenterol Rep. 2010;12(5):319-330. doi:10.1007/s11894-010-0131-2 EDN: RSMNCJ</mixed-citation></citation-alternatives></ref><ref id="B147"><label>147.</label><citation-alternatives><mixed-citation xml:lang="en">147.	Schröder JM, Harder J. Human beta-defensin-2. Int J Biochem Cell Biol. 1999;31(6):645-651. doi:10.1016/s1357-2725(99)00013-8 EDN: ACYFAN</mixed-citation><mixed-citation xml:lang="ru">147.	Matsui T, Amagai M. Dissecting the formation, structure and barrier function of the stratum corneum. Int Immunol. 2015;27(6):269-280. doi:10.1093/intimm/dxv013</mixed-citation></citation-alternatives></ref><ref id="B148"><label>148.</label><citation-alternatives><mixed-citation xml:lang="en">148.	Takizawa H. Airway epithelial cells as regulators of airway inflammation (Review). Int J Mol Med. 1998;1(2):367-378. doi:10.3892/ijmm.1.2.367</mixed-citation><mixed-citation xml:lang="ru">148.	Matsui T., Amagai, M. Erratum in Corrigendum, Int Immunol. 2017;29(5), 243-244. https://doi.org/10.1093/intimm/dxx024</mixed-citation></citation-alternatives></ref><ref id="B149"><label>149.</label><citation-alternatives><mixed-citation xml:lang="en">149.	Dockray GJ, Varro A, Dimaline R. Gastric endocrine cells: gene expression, processing, and targeting of active products. Physiol Rev. 1996;76(3):767-798. doi:10.1152/physrev.1996.76.3.767</mixed-citation><mixed-citation xml:lang="ru">149.	Schröder JM, Harder J. Human beta-defensin-2. Int J Biochem Cell Biol. 1999;31(6):645-651. doi:10.1016/s1357-2725(99)00013-8 EDN: ACYFAN</mixed-citation></citation-alternatives></ref><ref id="B150"><label>150.</label><citation-alternatives><mixed-citation xml:lang="en">150.	Yurchenco PD. Basement membranes: cell scaffoldings and signaling platforms. Cold Spring Harb Perspect Biol. 2011;3(2):a004911. doi:10.1101/cshperspect.a004911 EDN: RKJAIP</mixed-citation><mixed-citation xml:lang="ru">150.	Takizawa H. Airway epithelial cells as regulators of airway inflammation (Review). Int J Mol Med. 1998;1(2):367-378. doi:10.3892/ijmm.1.2.367</mixed-citation></citation-alternatives></ref><ref id="B151"><label>151.</label><citation-alternatives><mixed-citation xml:lang="en">151.	Kawanishi K. Diverse properties of the mesothelial cells in health and disease. Pleura Peritoneum. 2016;1(2):79-89. doi:10.1515/pp-2016-0009</mixed-citation><mixed-citation xml:lang="ru">151.	Dockray GJ, Varro A, Dimaline R. Gastric endocrine cells: gene expression, processing, and targeting of active products. Physiol Rev. 1996;76(3):767-798. doi:10.1152/physrev.1996.76.3.767</mixed-citation></citation-alternatives></ref><ref id="B152"><label>152.</label><citation-alternatives><mixed-citation xml:lang="en">152.	Ren J, Xiao YJ, Singh LS, et al. Lysophosphatidic acid is constitutively produced by human peritoneal mesothelial cells and enhances adhesion, migration, and invasion of ovarian cancer cells. Cancer Res. 2006;66(6):3006-3014. doi:10.1158/0008-5472.CAN-05-1292</mixed-citation><mixed-citation xml:lang="ru">152.	Yurchenco PD. Basement membranes: cell scaffoldings and signaling platforms. Cold Spring Harb Perspect Biol. 2011;3(2):a004911. doi:10.1101/cshperspect.a004911 EDN: RKJAIP</mixed-citation></citation-alternatives></ref><ref id="B153"><label>153.</label><citation-alternatives><mixed-citation xml:lang="en">153.	Silvestri R, Colucci E, Piccardi M, et al. Decoding the role of mesothelin in tumor dynamics and targeted treatment innovations. Mol Biomed. 2025;6(1):131. doi:10.1186/s43556-025-00379-z EDN: YYYJDL</mixed-citation><mixed-citation xml:lang="ru">153.	Kawanishi K. Diverse properties of the mesothelial cells in health and disease. Pleura Peritoneum. 2016;1(2):79-89. doi:10.1515/pp-2016-0009</mixed-citation></citation-alternatives></ref><ref id="B154"><label>154.</label><citation-alternatives><mixed-citation xml:lang="en">154.	Liu Y, Dong Z, Liu H, et al. Transition of mesothelial cell to fibroblast in peritoneal dialysis: EMT, stem cell or bystander?. Perit Dial Int. 2015;35(1):14-25. doi:10.3747/pdi.2014.00188</mixed-citation><mixed-citation xml:lang="ru">154.	Ren J, Xiao YJ, Singh LS, et al. Lysophosphatidic acid is constitutively produced by human peritoneal mesothelial cells and enhances adhesion, migration, and invasion of ovarian cancer cells. Cancer Res. 2006;66(6):3006-3014. doi:10.1158/0008-5472.CAN-05-1292</mixed-citation></citation-alternatives></ref><ref id="B155"><label>155.</label><citation-alternatives><mixed-citation xml:lang="en">155.	Offner FA, Feichtinger H, Stadlmann S, et al. Transforming growth factor-beta synthesis by human peritoneal mesothelial cells. Induction by interleukin-1. Am J Pathol. 1996;148(5):1679-1688.</mixed-citation><mixed-citation xml:lang="ru">155.	Silvestri R, Colucci E, Piccardi M, et al. Decoding the role of mesothelin in tumor dynamics and targeted treatment innovations. Mol Biomed. 2025;6(1):131. doi:10.1186/s43556-025-00379-z EDN: YYYJDL</mixed-citation></citation-alternatives></ref><ref id="B156"><label>156.</label><citation-alternatives><mixed-citation xml:lang="en">156.	Nielsen S, Frøkiaer J, Marples D, et al. Aquaporins in the kidney: from molecules to medicine. Physiol Rev. 2002;82(1):205-244. doi:10.1152/physrev.00024.2001 EDN: LRVRRL</mixed-citation><mixed-citation xml:lang="ru">156.	Liu Y, Dong Z, Liu H, et al. Transition of mesothelial cell to fibroblast in peritoneal dialysis: EMT, stem cell or bystander?. Perit Dial Int. 2015;35(1):14-25. doi:10.3747/pdi.2014.00188</mixed-citation></citation-alternatives></ref><ref id="B157"><label>157.</label><citation-alternatives><mixed-citation xml:lang="en">157.	Wolf MTF, Zhang J, Nie M. Uromodulin in mineral metabolism. Curr Opin Nephrol Hypertens. 2019;28(5):481-489. doi:10.1097/MNH.0000000000000522</mixed-citation><mixed-citation xml:lang="ru">157.	Offner FA, Feichtinger H, Stadlmann S, et al. Transforming growth factor-beta synthesis by human peritoneal mesothelial cells. Induction by interleukin-1. Am J Pathol. 1996;148(5):1679-1688.</mixed-citation></citation-alternatives></ref><ref id="B158"><label>158.</label><citation-alternatives><mixed-citation xml:lang="en">158.	Rotondi S, Pasquali M, Tartaglione L, et al. Soluble α -Klotho Serum Levels in Chronic Kidney Disease. Int J Endocrinol. 2015;2015:872193. doi:10.1155/2015/872193</mixed-citation><mixed-citation xml:lang="ru">158.	Nielsen S, Frøkiaer J, Marples D, et al. Aquaporins in the kidney: from molecules to medicine. Physiol Rev. 2002;82(1):205-244. doi:10.1152/physrev.00024.2001 EDN: LRVRRL</mixed-citation></citation-alternatives></ref><ref id="B159"><label>159.</label><citation-alternatives><mixed-citation xml:lang="en">159.	Young K, Beggs MR, Grimbly C, Alexander RT. Regulation of 1 and 24 hydroxylation of vitamin D metabolites in the proximal tubule. Exp Biol Med (Maywood). 2022;247(13):1103-1111. doi:10.1177/15353702221091982 EDN: CDNEIJ</mixed-citation><mixed-citation xml:lang="ru">159.	Wolf MTF, Zhang J, Nie M. Uromodulin in mineral metabolism. Curr Opin Nephrol Hypertens. 2019;28(5):481-489. doi:10.1097/MNH.0000000000000522</mixed-citation></citation-alternatives></ref><ref id="B160"><label>160.</label><citation-alternatives><mixed-citation xml:lang="en">160.	Wilson JL, Miranda CA, Knepper MA. Vasopressin and the regulation of aquaporin-2. Clin Exp Nephrol. 2013;17(6):751-764. doi:10.1007/s10157-013-0789-5 EDN: SSSTUL</mixed-citation><mixed-citation xml:lang="ru">160.	Rotondi S, Pasquali M, Tartaglione L, et al. Soluble α -Klotho Serum Levels in Chronic Kidney Disease. Int J Endocrinol. 2015;2015:872193. doi:10.1155/2015/872193</mixed-citation></citation-alternatives></ref><ref id="B161"><label>161.</label><citation-alternatives><mixed-citation xml:lang="en">161.	Katz AI. Renal Na-K-ATPase: its role in tubular sodium and potassium transport. Am J Physiol. 1982;242(3):F207-F219. doi:10.1152/ajprenal.1982.242.3.F207</mixed-citation><mixed-citation xml:lang="ru">161.	Young K, Beggs MR, Grimbly C, Alexander RT. Regulation of 1 and 24 hydroxylation of vitamin D metabolites in the proximal tubule. Exp Biol Med (Maywood). 2022;247(13):1103-1111. doi:10.1177/15353702221091982 EDN: CDNEIJ</mixed-citation></citation-alternatives></ref><ref id="B162"><label>162.</label><citation-alternatives><mixed-citation xml:lang="en">162.	Neubauer K, Zieger B. Endothelial cells and coagulation. Cell Tissue Res. 2022;387(3):391-398. doi:10.1007/s00441-021-03471-2 EDN: DEKJGJ</mixed-citation><mixed-citation xml:lang="ru">162.	Wilson JL, Miranda CA, Knepper MA. Vasopressin and the regulation of aquaporin-2. Clin Exp Nephrol. 2013;17(6):751-764. doi:10.1007/s10157-013-0789-5 EDN: SSSTUL</mixed-citation></citation-alternatives></ref><ref id="B163"><label>163.</label><citation-alternatives><mixed-citation xml:lang="en">163.	McEver RP. Selectins: initiators of leucocyte adhesion and signalling at the vascular wall. Cardiovasc Res. 2015;107(3):331-339. doi:10.1093/cvr/cvv154</mixed-citation><mixed-citation xml:lang="ru">163.	Katz AI. Renal Na-K-ATPase: its role in tubular sodium and potassium transport. Am J Physiol. 1982;242(3):F207-F219. doi:10.1152/ajprenal.1982.242.3.F207</mixed-citation></citation-alternatives></ref><ref id="B164"><label>164.</label><citation-alternatives><mixed-citation xml:lang="en">164.	Lowenstein CJ, Morrell CN, Yamakuchi M. Regulation of Weibel-Palade body exocytosis. Trends Cardiovasc Med. 2005;15(8):302-308. doi:10.1016/j.tcm.2005.09.005</mixed-citation><mixed-citation xml:lang="ru">164.	Neubauer K, Zieger B. Endothelial cells and coagulation. Cell Tissue Res. 2022;387(3):391-398. doi:10.1007/s00441-021-03471-2 EDN: DEKJGJ</mixed-citation></citation-alternatives></ref><ref id="B165"><label>165.</label><citation-alternatives><mixed-citation xml:lang="en">165.	Maroney SA, Mast AE. New insights into the biology of tissue factor pathway inhibitor. J Thromb Haemost. 2015;13 Suppl 1(0 1):S200-S207. doi:10.1111/jth.12897</mixed-citation><mixed-citation xml:lang="ru">165.	McEver RP. Selectins: initiators of leucocyte adhesion and signalling at the vascular wall. Cardiovasc Res. 2015;107(3):331-339. doi:10.1093/cvr/cvv154</mixed-citation></citation-alternatives></ref><ref id="B166"><label>166.</label><citation-alternatives><mixed-citation xml:lang="en">166.	Lupu C, Poulsen E, Roquefeuil S, et al. Cellular effects of heparin on the production and release of tissue factor pathway inhibitor in human endothelial cells in culture. Arterioscler Thromb Vasc Biol. 1999;19(9):2251-2262. doi:10.1161/01.atv.19.9.2251</mixed-citation><mixed-citation xml:lang="ru">166.	Lowenstein CJ, Morrell CN, Yamakuchi M. Regulation of Weibel-Palade body exocytosis. Trends Cardiovasc Med. 2005;15(8):302-308. doi:10.1016/j.tcm.2005.09.005</mixed-citation></citation-alternatives></ref><ref id="B167"><label>167.</label><citation-alternatives><mixed-citation xml:lang="en">167.	Reitsma S, Slaaf DW, Vink H, et al. The endothelial glycocalyx: composition, functions, and visualization. Pflugers Arch. 2007;454(3):345-359. doi:10.1007/s00424-007-0212-8 EDN: BWZRUW</mixed-citation><mixed-citation xml:lang="ru">167.	Maroney SA, Mast AE. New insights into the biology of tissue factor pathway inhibitor. J Thromb Haemost. 2015;13 Suppl 1(0 1):S200-S207. doi:10.1111/jth.12897</mixed-citation></citation-alternatives></ref><ref id="B168"><label>168.</label><citation-alternatives><mixed-citation xml:lang="en">168.	Tousoulis D, Kampoli AM, Tentolouris C, et al. The role of nitric oxide on endothelial function. Curr Vasc Pharmacol. 2012;10(1):4-18. doi:10.2174/157016112798829760</mixed-citation><mixed-citation xml:lang="ru">168.	Lupu C, Poulsen E, Roquefeuil S, et al. Cellular effects of heparin on the production and release of tissue factor pathway inhibitor in human endothelial cells in culture. Arterioscler Thromb Vasc Biol. 1999;19(9):2251-2262. doi:10.1161/01.atv.19.9.2251</mixed-citation></citation-alternatives></ref><ref id="B169"><label>169.</label><citation-alternatives><mixed-citation xml:lang="en">169.	Marin V, Montero-Julian FA, Grès S, et al. The IL-6-soluble IL-6Ralpha autocrine loop of endothelial activation as an intermediate between acute and chronic inflammation: an experimental model involving thrombin. J Immunol. 2001;167(6):3435-3442. doi:10.4049/jimmunol.167.6.3435</mixed-citation><mixed-citation xml:lang="ru">169.	Reitsma S, Slaaf DW, Vink H, et al. The endothelial glycocalyx: composition, functions, and visualization. Pflugers Arch. 2007;454(3):345-359. doi:10.1007/s00424-007-0212-8 EDN: BWZRUW</mixed-citation></citation-alternatives></ref><ref id="B170"><label>170.</label><citation-alternatives><mixed-citation xml:lang="en">170.	Li Y, Chi L, Stechschulte DJ, Dileepan KN. Histamine-induced production of interleukin-6 and interleukin-8 by human coronary artery endothelial cells is enhanced by endotoxin and tumor necrosis factor-alpha. Microvasc Res. 2001;61(3):253-262. doi:10.1006/mvre.2001.2304</mixed-citation><mixed-citation xml:lang="ru">170.	Tousoulis D, Kampoli AM, Tentolouris C, et al. The role of nitric oxide on endothelial function. Curr Vasc Pharmacol. 2012;10(1):4-18. doi:10.2174/157016112798829760</mixed-citation></citation-alternatives></ref><ref id="B171"><label>171.</label><citation-alternatives><mixed-citation xml:lang="en">171.	Witjas FMR, van den Berg BM, van den Berg CW, et al. Concise Review: The Endothelial Cell Extracellular Matrix Regulates Tissue Homeostasis and Repair. Stem Cells Transl Med. 2019;8(4):375-382. doi:10.1002/sctm.18-0155</mixed-citation><mixed-citation xml:lang="ru">171.	Marin V, Montero-Julian FA, Grès S, et al. The IL-6-soluble IL-6Ralpha autocrine loop of endothelial activation as an intermediate between acute and chronic inflammation: an experimental model involving thrombin. J Immunol. 2001;167(6):3435-3442. doi:10.4049/jimmunol.167.6.3435</mixed-citation></citation-alternatives></ref><ref id="B172"><label>172.</label><citation-alternatives><mixed-citation xml:lang="en">172.	Xu L, Nirwane A, Yao Y. Basement membrane and blood-brain barrier. Stroke Vasc Neurol. 2018;4(2):78-82. doi:10.1136/svn-2018-000198</mixed-citation><mixed-citation xml:lang="ru">172.	Li Y, Chi L, Stechschulte DJ, Dileepan KN. Histamine-induced production of interleukin-6 and interleukin-8 by human coronary artery endothelial cells is enhanced by endotoxin and tumor necrosis factor-alpha. Microvasc Res. 2001;61(3):253-262. doi:10.1006/mvre.2001.2304</mixed-citation></citation-alternatives></ref><ref id="B173"><label>173.</label><citation-alternatives><mixed-citation xml:lang="en">173.	Deev RV. Pathomorphogenesis of some diseases and conditions with an ischemic component and clinical and morphological analysis of gene-induced angiogenesis used for their correction. In: Collection of scientific papers of the All-Russian conference with international participation "Modern approaches to clinical and morphological diagnostics of human diseases", VII scientific readings dedicated to the 100th anniversary of Corresponding Member of the Russian Academy of Medical Sciences, Honored Scientist of the Russian Federation, Professor Oleg Konstantinovich Khmelnitsky. February 12, 2021. St. Petersburg, 47-54. (In Russ.)</mixed-citation><mixed-citation xml:lang="ru">173.	Witjas FMR, van den Berg BM, van den Berg CW, et al. Concise Review: The Endothelial Cell Extracellular Matrix Regulates Tissue Homeostasis and Repair. Stem Cells Transl Med. 2019;8(4):375-382. doi:10.1002/sctm.18-0155</mixed-citation></citation-alternatives></ref><ref id="B174"><label>174.</label><citation-alternatives><mixed-citation xml:lang="en">174.	Santillán-Cortez D, Vera-Gómez E, Hernández-Patricio A, et al. Endothelial Progenitor Cells May Be Related to Major Amputation after Angioplasty in Patients with Critical Limb Ischemia. Cells. 2023; 12(4):584. doi: 10.3390/cells12040584 EDN: DFYSJQ</mixed-citation><mixed-citation xml:lang="ru">174.	Xu L, Nirwane A, Yao Y. Basement membrane and blood-brain barrier. Stroke Vasc Neurol. 2018;4(2):78-82. doi:10.1136/svn-2018-000198</mixed-citation></citation-alternatives></ref><ref id="B175"><label>175.</label><citation-alternatives><mixed-citation xml:lang="en">175.	Balaji S, King A, Crombleholme TM, Keswani SG. The Role of Endothelial Progenitor Cells in Postnatal Vasculogenesis: Implications for Therapeutic Neovascularization and Wound Healing. Adv Wound Care (New Rochelle). 2013;2(6):283-295. doi:10.1089/wound.2012.0398</mixed-citation><mixed-citation xml:lang="ru">175.	Deev RV. Pathomorphogenesis of some diseases and conditions with an ischemic component and clinical and morphological analysis of gene-induced angiogenesis used for their correction. In: Collection of scientific papers of the All-Russian conference with international participation "Modern approaches to clinical and morphological diagnostics of human diseases", VII scientific readings dedicated to the 100th anniversary of Corresponding Member of the Russian Academy of Medical Sciences, Honored Scientist of the Russian Federation, Professor Oleg Konstantinovich Khmelnitsky. February 12, 2021. St. Petersburg, 47-54. (In Russ.)</mixed-citation></citation-alternatives></ref><ref id="B176"><label>176.</label><citation-alternatives><mixed-citation xml:lang="en">176.	Vinci MC, Carulli E, Rurali E, et al. The Long Telling Story of "Endothelial Progenitor Cells": Where Are We at Now?. Cells. 2022;12(1):112. doi:10.3390/cells12010112</mixed-citation><mixed-citation xml:lang="ru">176.	Santillán-Cortez D, Vera-Gómez E, Hernández-Patricio A, et al. Endothelial Progenitor Cells May Be Related to Major Amputation after Angioplasty in Patients with Critical Limb Ischemia. Cells. 2023; 12(4):584. doi: 10.3390/cells12040584 EDN: DFYSJQ</mixed-citation></citation-alternatives></ref><ref id="B177"><label>177.</label><citation-alternatives><mixed-citation xml:lang="en">177.	Parham KA, Pitson SM, Bonder CS. Regulation of EPCs: The Gateway to Blood Vessel Formation, New Journal of Science, 2014;972043(16). doi:10.1155/2014/972043</mixed-citation><mixed-citation xml:lang="ru">177.	Balaji S, King A, Crombleholme TM, Keswani SG. The Role of Endothelial Progenitor Cells in Postnatal Vasculogenesis: Implications for Therapeutic Neovascularization and Wound Healing. Adv Wound Care (New Rochelle). 2013;2(6):283-295. doi:10.1089/wound.2012.0398</mixed-citation></citation-alternatives></ref><ref id="B178"><label>178.</label><citation-alternatives><mixed-citation xml:lang="en">178.	Carmeliet P. Angiogenesis in life, disease and medicine. Nature 2005; 438: 932-6.</mixed-citation><mixed-citation xml:lang="ru">178.	Vinci MC, Carulli E, Rurali E, et al. The Long Telling Story of "Endothelial Progenitor Cells": Where Are We at Now?. Cells. 2022;12(1):112. doi:10.3390/cells12010112</mixed-citation></citation-alternatives></ref><ref id="B179"><label>179.</label><citation-alternatives><mixed-citation xml:lang="en">179.	Pugh CW, Ratcliffe PJ. Regulation of angiogenesis by hipoxia: HIF system. Nat Medicine. 2003; 9:677-684.</mixed-citation><mixed-citation xml:lang="ru">179.	Parham KA, Pitson SM, Bonder CS. Regulation of EPCs: The Gateway to Blood Vessel Formation, New Journal of Science, 2014;972043(16). doi:10.1155/2014/972043</mixed-citation></citation-alternatives></ref><ref id="B180"><label>180.</label><citation-alternatives><mixed-citation xml:lang="en">180.	Duran CL, Howell DW, Dave JM et al. Molecular Regulation of Sprouting Angiogenesis. Compr Physiol. 2017; 8(1):153-235. doi: 10.1002/cphy.c160048</mixed-citation><mixed-citation xml:lang="ru">180.	Carmeliet P. Angiogenesis in life, disease and medicine. Nature 2005; 438: 932-6.</mixed-citation></citation-alternatives></ref><ref id="B181"><label>181.</label><citation-alternatives><mixed-citation xml:lang="en">181.	Makanya AN, Hlushchuk R, Djonov VG. Intussusceptive angiogenesis and its role in vascular morphogenesis, patterning, and remodeling. Angiogenesis 2009; 12(2): 113-23. DOI: 10.1007/s10456-009-9129-5 EDN: LUNNBP</mixed-citation><mixed-citation xml:lang="ru">181.	Pugh CW, Ratcliffe PJ. Regulation of angiogenesis by hipoxia: HIF system. Nat Medicine. 2003; 9:677-684.</mixed-citation></citation-alternatives></ref><ref id="B182"><label>182.</label><citation-alternatives><mixed-citation xml:lang="en">182.	Isner JM, Feldman LJ. Gene therapy for arterial disease. Lancet 1994; 344(8938): 1653-4. DOI: 10.1016/s0140-6736(94)90454-5 EDN: BVRIDJ</mixed-citation><mixed-citation xml:lang="ru">182.	Duran CL, Howell DW, Dave JM et al. Molecular Regulation of Sprouting Angiogenesis. Compr Physiol. 2017; 8(1):153-235. doi: 10.1002/cphy.c160048</mixed-citation></citation-alternatives></ref><ref id="B183"><label>183.</label><citation-alternatives><mixed-citation xml:lang="en">183.	Urbich C, Dimmeler S. Endothelial progenitor cells: characterization and role in vascular biology. Circ. Res. 2004; 95(4): 343-53. DOI: 10.1161/01.RES.0000137877.89448.78</mixed-citation><mixed-citation xml:lang="ru">183.	Makanya AN, Hlushchuk R, Djonov VG. Intussusceptive angiogenesis and its role in vascular morphogenesis, patterning, and remodeling. Angiogenesis 2009; 12(2): 113-23. DOI: 10.1007/s10456-009-9129-5 EDN: LUNNBP</mixed-citation></citation-alternatives></ref><ref id="B184"><label>184.</label><citation-alternatives><mixed-citation xml:lang="en">184.	Rizov M, Andreeva P, Dimova I. Molecular regulation and role of angiogenesis in reproduction. Taiwan J Obstet Gynecol. 2017; 56(2):127-132. doi: 10.1016/j.tjog.2016.06.019</mixed-citation><mixed-citation xml:lang="ru">184.	Isner JM, Feldman LJ. Gene therapy for arterial disease. Lancet 1994; 344(8938): 1653-4. DOI: 10.1016/s0140-6736(94)90454-5 EDN: BVRIDJ</mixed-citation></citation-alternatives></ref><ref id="B185"><label>185.</label><citation-alternatives><mixed-citation xml:lang="en">185.	Aicher A., Heeschen C., Mildner-Rihm C. et al. Essential role of endothelial nitric oxide synthase for mobilization of stem and progenitor cells. Nat. Med. 2003; 9: 1370-6. doi: 10.1038/nm948</mixed-citation><mixed-citation xml:lang="ru">185.	Urbich C, Dimmeler S. Endothelial progenitor cells: characterization and role in vascular biology. Circ. Res. 2004; 95(4): 343-53. DOI: 10.1161/01.RES.0000137877.89448.78</mixed-citation></citation-alternatives></ref><ref id="B186"><label>186.</label><citation-alternatives><mixed-citation xml:lang="en">186.	De Falco E., Porcelli D., Torella A.R. et al. SDF-1 involvement in endothelial phenotype and ischemia-induced recruitment of bone marrow progenitor cells. Blood 2004; 104: 3472-82. doi: 10.1182/blood-2003-12-4423</mixed-citation><mixed-citation xml:lang="ru">186.	Rizov M, Andreeva P, Dimova I. Molecular regulation and role of angiogenesis in reproduction. Taiwan J Obstet Gynecol. 2017; 56(2):127-132. doi: 10.1016/j.tjog.2016.06.019</mixed-citation></citation-alternatives></ref><ref id="B187"><label>187.</label><citation-alternatives><mixed-citation xml:lang="en">187.	Bozo I. Ya., Deev R. V., Pinaev G. P. "Fibroblast" - a specialized cell or a functional state of cells of mesenchymal origin? Tsitologiya 2010; 52(2): 99-109. (In Russ.) EDN: OJRWGB</mixed-citation><mixed-citation xml:lang="ru">187.	Aicher A., Heeschen C., Mildner-Rihm C. et al. Essential role of endothelial nitric oxide synthase for mobilization of stem and progenitor cells. Nat. Med. 2003; 9: 1370-6. doi: 10.1038/nm948</mixed-citation></citation-alternatives></ref><ref id="B188"><label>188.</label><citation-alternatives><mixed-citation xml:lang="en">188. Iruela-Arispe ML, Davis GE. Cellular and molecular mechanisms of vascular lumen formation. Dev Cell. 2009; 16(2):222-31. doi: 10.1016/j.devcel.2009.01.013.</mixed-citation><mixed-citation xml:lang="ru">188.	De Falco E., Porcelli D., Torella A.R. et al. SDF-1 involvement in endothelial phenotype and ischemia-induced recruitment of bone marrow progenitor cells. Blood 2004; 104: 3472-82. doi: 10.1182/blood-2003-12-4423</mixed-citation></citation-alternatives></ref><ref id="B189"><label>189.</label><citation-alternatives><mixed-citation xml:lang="en">189.	Lammert E, Axnick J. Vascular lumen formation.</mixed-citation><mixed-citation xml:lang="ru">189.	Bozo I. Ya., Deev R. V., Pinaev G. P. "Fibroblast" - a specialized cell or a functional state of cells of mesenchymal origin? Tsitologiya 2010; 52(2): 99-109. (In Russ.) EDN: OJRWGB</mixed-citation></citation-alternatives></ref><ref id="B190"><label>190.</label><citation-alternatives><mixed-citation xml:lang="en">Cold Spring Harb Perspect Med. 2012; 2(4):a006619. DOI: 10.1101/cshperspect.a006619</mixed-citation><mixed-citation xml:lang="ru">190. Iruela-Arispe ML, Davis GE. Cellular and molecular mechanisms of vascular lumen formation. Dev Cell. 2009; 16(2):222-31. doi: 10.1016/j.devcel.2009.01.013.</mixed-citation></citation-alternatives></ref><ref id="B191"><label>191.</label><citation-alternatives><mixed-citation xml:lang="en">190.	Cherednichenko VR, Khovantseva US, Kuzmin VV, et al. Modeling the processes of transendothelial transport of LDL and macrophage migration. Russ J Immunol. 2024; 27(3): 499-504. (In Russ.) https://doi.org/10.46235/1028-7221-16678-MTP EDN: AHKHYA</mixed-citation><mixed-citation xml:lang="ru">191.	Lammert E, Axnick J. Vascular lumen formation.</mixed-citation></citation-alternatives></ref><ref id="B192"><label>192.</label><mixed-citation>Cold Spring Harb Perspect Med. 2012; 2(4):a006619. DOI: 10.1101/cshperspect.a006619</mixed-citation></ref><ref id="B193"><label>193.</label><mixed-citation>192.	Cherednichenko VR, Khovantseva US, Kuzmin VV, et al. Modeling the processes of transendothelial transport of LDL and macrophage migration. Russ J Immunol. 2024; 27(3): 499-504. (In Russ.) https://doi.org/10.46235/1028-7221-16678-MTP EDN: AHKHYA</mixed-citation></ref></ref-list></back></article>
