<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE root>
<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="research-article" 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">629037</article-id><article-id pub-id-type="doi">10.17816/morph.629037</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>Original Study Articles</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>Оригинальные исследования</subject></subj-group><subj-group subj-group-type="article-type"><subject>Research Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">Сonnexin-43 in cells of injured rat sciatic nerve</article-title><trans-title-group xml:lang="ru"><trans-title>Коннексин-43 в клетках регенерирующего седалищного нерва крысы</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-9643-6831</contrib-id><contrib-id contrib-id-type="spin">1479-5992</contrib-id><name-alternatives><name xml:lang="en"><surname>Kolos</surname><given-names>Elena A.</given-names></name><name xml:lang="ru"><surname>Колос</surname><given-names>Елена Андреевна</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>koloselena1984@yandex.ru</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Institute of Experimental Medicine</institution></aff><aff><institution xml:lang="ru">Институт экспериментальной медицины</institution></aff></aff-alternatives><pub-date date-type="preprint" iso-8601-date="2024-04-18" publication-format="electronic"><day>18</day><month>04</month><year>2024</year></pub-date><pub-date date-type="pub" iso-8601-date="2023-07-15" publication-format="electronic"><day>15</day><month>07</month><year>2023</year></pub-date><volume>161</volume><issue>3</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>71</fpage><lpage>78</lpage><history><date date-type="received" iso-8601-date="2024-03-13"><day>13</day><month>03</month><year>2024</year></date><date date-type="accepted" iso-8601-date="2024-04-12"><day>12</day><month>04</month><year>2024</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2023, Eco-Vector</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2023, Эко-Вектор</copyright-statement><copyright-year>2023</copyright-year><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="2026-07-15"/><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/629037">https://j-morphology.com/1026-3543/article/view/629037</self-uri><abstract xml:lang="en"><p><bold>BACKGROUND:</bold> It is known that intercellular communications in the peripheral nervous system are provided by various types of intercellular contacts, in particular, gap junctions formed by connexin proteins. The literature contains data on changes in the expression of connexin-32, connexin-46 and other types of connexins during nerve injury. However, very few studies describe changes in connexin-43 expression in similar pathologies.</p> <p><bold>AIM:</bold> The purpose of this study was to study the distribution and localization of the gap junction protein connexin-43 (Cx43) in cells of intact and injured rat sciatic nerve.</p> <p><bold>MATERIALS AND METHODS:</bold> Damage to the sciatic nerves of Wistar rats of the experimental group (n=5) was carried out by nerve ligation for 40 s. Animals without damage of sciatic nerve were studied as a control group (n=5). Immunohistochemical detection of Cx43 was performed on paraffin sections.</p> <p><bold>RESULTS:</bold> It has been established that the protein is contained in the cells of the perineurium and epineurium of both the intact nerve and after the application of a ligature. In the area of the endoneurium, in the absence of nerve damage, Cx43 is detected only in the endotheliocytes of a few vessels. In the endoneurium of the injured nerve, a large number of large Cx43-immunopositive cells with processes were identified.</p> <p><bold>CONCLUSIONS:</bold> It has been established that Cx43-containing cells are identified in the endoneurium of the sciatic nerve only after damage. To clarify whether such cells belong to a specific cell type, additional studies are necessary.</p></abstract><trans-abstract xml:lang="ru"><p><bold>Обоснование.</bold> Известно, что межклеточные коммуникации в периферической нервной системе обеспечивают различные виды межклеточных контактов, в частности щелевые контакты, сформированные белками коннексинами. В литературе присутствуют данные об изменении экспрессии коннексина-32, коннексина-46 и других типов коннексинов при травме нерва. Однако крайне мало исследований описывают изменение экспрессии коннексина-43 при аналогичной патологии.</p> <p><bold>Цель исследования</bold> — изучить распределение и локализацию белка щелевых контактов коннексина-43 (Сх43) в клетках интактного и повреждённого седалищного нерва крысы.</p> <p><bold>Материалы и методы.</bold> Повреждение седалищных нервов крыс линии Вистар подопытной группы (<italic>n</italic>=5) было выполнено путём наложения лигатуры в течение 40 с. В качестве группы контроля (<italic>n</italic>=5) исследованы животные без повреждения седалищного нерва. На парафиновых срезах проводили иммуногистохимическое выявление Сх43.</p> <p><bold>Результаты.</bold> Установлено, что Сх43 содержится в клетках периневрия и эпиневрия как интактного нерва, так и нерва после наложения лигатуры. В области эндоневрия при отсутствии повреждения нерва Сх43 выявляется лишь в эндотелиоцитах немногочисленных сосудов. В эндоневрии повреждённого нерва идентифицируется большое количество крупных отростчатых Cx43-иммунопозитивных клеток.</p> <p><bold>Заключение.</bold> Установлено, что Cx43-содержащие клетки идентифицируются в эндоневрии седалищного нерва только после повреждения. Для уточнения принадлежности таких клеток эндоневрия к определённому клеточному типу необходимы дополнительные исследования.</p></trans-abstract><kwd-group xml:lang="en"><kwd>connexin-43</kwd><kwd>Cx43</kwd><kwd>sciatic nerve</kwd><kwd>immunohistochemistry</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>коннексин-43</kwd><kwd>Cx43</kwd><kwd>седалищный нерв</kwd><kwd>иммуногистохимия</kwd></kwd-group><funding-group><award-group><funding-source><institution-wrap><institution xml:lang="ru">Российский научный фонд</institution></institution-wrap><institution-wrap><institution xml:lang="en">Russian Science Foundation</institution></institution-wrap></funding-source><award-id>23-25-10003</award-id></award-group><award-group><funding-source><institution-wrap><institution xml:lang="ru">Санкт-Петербургский научный фонд</institution></institution-wrap><institution-wrap><institution xml:lang="en">Saint Petersburg Science Foundation</institution></institution-wrap></funding-source><award-id>23-25-10003</award-id></award-group></funding-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><citation-alternatives><mixed-citation xml:lang="en">Lavorato A, Aruta G, De Marco R, et al. Traumatic peripheral nerve injuries: a classification proposal. J Orthop Traumatol. 2023;24(1):20. doi: 10.1186/s10195-023-00695-6</mixed-citation><mixed-citation xml:lang="ru">Lavorato A., Aruta G., De Marco R., et al. Traumatic peripheral nerve injuries: a classification proposal // J Orthop Traumatol. 2023. Vol. 24, N 1. P. 20. doi: 10.1186/s10195-023-00695-6</mixed-citation></citation-alternatives></ref><ref id="B2"><label>2.</label><citation-alternatives><mixed-citation xml:lang="en">Menorca RM, Fussell TS, Elfar JC. Nerve physiology: mechanisms of injury and recovery. Hand Clin. 2013;29(3):317–330. doi: 10.1016/j.hcl.2013.04.002</mixed-citation><mixed-citation xml:lang="ru">Menorca R.M., Fussell T.S., Elfar J.C. Nerve physiology: mechanisms of injury and recovery // Hand Clin. 2013. Vol. 29, N 3. P. 317–330. doi: 10.1016/j.hcl.2013.04.002</mixed-citation></citation-alternatives></ref><ref id="B3"><label>3.</label><citation-alternatives><mixed-citation xml:lang="en">Chandross KJ, Kessler JA, Cohen RI, et al. Altered connexin expression after peripheral nerve injury. Mol Cell Neurosci. 1996;7(6):501–518. doi: 10.1006/mcne.1996.0036</mixed-citation><mixed-citation xml:lang="ru">Chandross K.J., Kessler J.A., Cohen R.I., et al. Altered connexin expression after peripheral nerve injury // Mol Cell Neurosci. 1996. Vol. 7, N 6. P. 501–518. doi: 10.1006/mcne.1996.0036</mixed-citation></citation-alternatives></ref><ref id="B4"><label>4.</label><citation-alternatives><mixed-citation xml:lang="en">Yoshimura T, Satake M, Kobayashi T. Connexin43 is another gap junction protein in the peripheral nervous system. J Neurochem. 1996;7(6):501–518. doi: 10.1046/j.1471-4159.1996.67031252.x</mixed-citation><mixed-citation xml:lang="ru">Yoshimura T., Satake M., Kobayashi T. Connexin43 is another gap junction protein in the peripheral nervous system // J Neurochem. 1996. Vol. 67, N 3. P. 1252–1258. doi: 10.1046/j.1471-4159.1996.67031252.x</mixed-citation></citation-alternatives></ref><ref id="B5"><label>5.</label><citation-alternatives><mixed-citation xml:lang="en">Altevogt BM, Kleopa KA, Postma FR, et al. Connexin29 is uniquely distributed within myelinating glial cells of the central and peripheral nervous systems. J Neurosci. 2002;22(15):6458–6470. doi: 10.1523/JNEUROSCI.22-15-06458.2002</mixed-citation><mixed-citation xml:lang="ru">Altevogt B.M., Kleopa K.A., Postma F.R., et al. Connexin29 is uniquely distributed within myelinating glial cells of the central and peripheral nervous systems // J Neurosci. 2002. Vol. 22, N 15. Р. 6458–6470. doi: 10.1523/JNEUROSCI.22-15-06458.2002</mixed-citation></citation-alternatives></ref><ref id="B6"><label>6.</label><citation-alternatives><mixed-citation xml:lang="en">Lin SH, Lu CY, Muhammad R, et al. Induction of connexin 37 expression in a rat model of neuropathic pain. Brain Res Mol Brain Res. 2002;99(2):134–140. doi: 10.1016/s0169-328x(02)00112-2</mixed-citation><mixed-citation xml:lang="ru">Lin S.H., Lu C.Y., Muhammad R., et al. Induction of connexin 37 expression in a rat model of neuropathic pain // Brain Res Mol Brain Res. 2002. Vol. 99, N 2. P. 134–140. doi: 10.1016/s0169-328x(02)00112-2</mixed-citation></citation-alternatives></ref><ref id="B7"><label>7.</label><citation-alternatives><mixed-citation xml:lang="en">Kolos EA, Korzhevsky DE. Gap junction protein connexin-43 in a rat dorsal root ganglion. Cell and Tissue Biology. 2024;18(2):189–198. doi: 10.1134/S1990519X23700049</mixed-citation><mixed-citation xml:lang="ru">Kolos E.A., Korzhevsky D.E. Gap junction protein connexin-43 in a rat dorsal root ganglion // Cell and Tissue Biology. 2024. Vol. 18, N 2. Р. 189–198. doi: 10.1134/S1990519X23700049</mixed-citation></citation-alternatives></ref><ref id="B8"><label>8.</label><citation-alternatives><mixed-citation xml:lang="en">Zhu Y. Gap junction-dependent and -independent functions of connexin43 in biology. Biology (Basel). 2022;11(2):283. doi: 10.3390/biology11020283</mixed-citation><mixed-citation xml:lang="ru">Zhu Y. Gap junction-dependent and -independent functions of connexin43 in biology // Biology (Basel). 2022. Vol. 11, N 2. P. 283. doi: 10.3390/biology11020283</mixed-citation></citation-alternatives></ref><ref id="B9"><label>9.</label><citation-alternatives><mixed-citation xml:lang="en">Dosch M, Zindel J, Jebbawi F, et al. Connexin-43-dependent ATP release mediates macrophage activation during sepsis. Elife. 2019;8:e42670. doi: 10.7554/eLife.42670</mixed-citation><mixed-citation xml:lang="ru">Dosch M., Zindel J., Jebbawi F., et al. Connexin-43-dependent ATP release mediates macrophage activation during sepsis // Elife. 2019. Vol. 8. P. e42670. doi: 10.7554/eLife.42670</mixed-citation></citation-alternatives></ref><ref id="B10"><label>10.</label><citation-alternatives><mixed-citation xml:lang="en">Kameritsch P, Pogoda K, Pohl U. Channel-independent influence of connexin 43 on cell migration. Biochim Biophys Acta. 2012;1818(8):1993–2001. doi: 10.1016/j.bbamem.2011.11.016</mixed-citation><mixed-citation xml:lang="ru">Kameritsch P., Pogoda K., Pohl U. Channel-independent influence of connexin 43 on cell migration // Biochim Biophys Acta. 2012. Vol. 1818, N 8. P. 1993–2001. doi: 10.1016/j.bbamem.2011.11.016</mixed-citation></citation-alternatives></ref><ref id="B11"><label>11.</label><citation-alternatives><mixed-citation xml:lang="en">Xie HY, Cui Y, Deng F, Feng JC. Connexin: a potential novel target for protecting the central nervous system? Neural Regen Res. 2015;10(4):659–666. doi: 10.4103/1673-5374.155444</mixed-citation><mixed-citation xml:lang="ru">Xie H.Y., Cui Y., Deng F., Feng J.C. Connexin: a potential novel target for protecting the central nervous system? // Neural Regen Res. 2015. Vol. 10, N 4. P. 659–666. doi: 10.4103/1673-5374.155444</mixed-citation></citation-alternatives></ref><ref id="B12"><label>12.</label><citation-alternatives><mixed-citation xml:lang="en">Ozawa H, Mutai H, Matsunaga T, et al. Promoted cell proliferation by connexin 30 gene transfection to head-and-neck cancer cell line. Anticancer Res. 2009;29(6):1981–1985.</mixed-citation><mixed-citation xml:lang="ru">Ozawa H., Mutai H., Matsunaga T., et al. Promoted cell proliferation by connexin 30 gene transfection to head-and-neck cancer cell line // Anticancer Res. 2009. Vol. 29, N 6. P. 1981–1985.</mixed-citation></citation-alternatives></ref><ref id="B13"><label>13.</label><citation-alternatives><mixed-citation xml:lang="en">Kutova OM, Pospelov AD, Balalaeva IV. The multifaceted role of connexins in tumor microenvironment initiation and maintenance. Biology (Basel). 2023;12(2):204. doi: 10.3390/biology12020204</mixed-citation><mixed-citation xml:lang="ru">Kutova O.M., Pospelov A.D., Balalaeva I.V. The multifaceted role of connexins in tumor microenvironment initiation and maintenance // Biology (Basel). 2023. Vol. 12, N 2. P. 204. doi: 10.3390/biology12020204</mixed-citation></citation-alternatives></ref><ref id="B14"><label>14.</label><citation-alternatives><mixed-citation xml:lang="en">Rodjakovic D, Salm L, Beldi G. Function of connexin-43 in macrophages. Int J Mol Sci. 2021;22(3):1412. doi: 10.3390/ijms22031412</mixed-citation><mixed-citation xml:lang="ru">Rodjakovic D., Salm L., Beldi G. Function of connexin-43 in macrophages // Int J Mol Sci. 2021. Vol. 22, N 3. P. 1412. doi: 10.3390/ijms22031412</mixed-citation></citation-alternatives></ref><ref id="B15"><label>15.</label><citation-alternatives><mixed-citation xml:lang="en">Cristovao B, Rodrigues L, Catarino S, et al. Cx43-mediated hyphal folding counteracts phagosome integrity loss during fungal infection. Microbiol Spectr. 2023;11(5):e0123823. doi: 10.1128/spectrum.01238-23</mixed-citation><mixed-citation xml:lang="ru">Cristovao B., Rodrigues L., Catarino S., et al. Cx43-mediated hyphal folding counteracts phagosome integrity loss during fungal infection // Microbiol Spectr. 2023. Vol. 11, N 5. P. e0123823. doi: 10.1128/spectrum.01238-23</mixed-citation></citation-alternatives></ref><ref id="B16"><label>16.</label><citation-alternatives><mixed-citation xml:lang="en">Li J, Habbes HW, Eiberger J, et al. Analysis of connexin expression during mouse Schwann cell development identifies connexin29 as a novel marker for the transition of neural crest to precursor cells. Glia. 2007;55(1):93–103. doi: 10.1002/glia.20427</mixed-citation><mixed-citation xml:lang="ru">Li J., Habbes H.W., Eiberger J., et al. Analysis of connexin expression during mouse Schwann cell development identifies connexin29 as a novel marker for the transition of neural crest to precursor cells // Glia. 2007. Vol. 55, N 1. P. 93–103. doi: 10.1002/glia.20427</mixed-citation></citation-alternatives></ref><ref id="B17"><label>17.</label><citation-alternatives><mixed-citation xml:lang="en">Zhao S, Spray DC. Localization of Cx26, Cx32, and Cx43 in myelinating Schwann cells of mouse sciatic nerve during postnatal development. In: Werner R, editor. Gap junctions. Amsterdam: IOS Press; 1997. Р. 198–202.</mixed-citation><mixed-citation xml:lang="ru">Zhao S., Spray D.C. Localization of Cx26, Cx32, and Cx43 in myelinating Schwann cells of mouse sciatic nerve during postnatal development. In: Werner R., editor. Gap junctions. Amsterdam: IOS Press, 1997. Р. 198–202.</mixed-citation></citation-alternatives></ref><ref id="B18"><label>18.</label><citation-alternatives><mixed-citation xml:lang="en">Mambetisaeva ET, Gire V, Evans WH. Multiple connexin expression in peripheral nerve, Schwann cells, and Schwannoma cells. J Neurosci Res. 1999;57(2):166–175. doi: 10.1002/(SICI)1097-4547(19990715)57:2&lt;166::AID-JNR2&gt;3.0.CO;2-Y</mixed-citation><mixed-citation xml:lang="ru">Mambetisaeva E.T., Gire V., Evans W.H. Multiple connexin expression in peripheral nerve, Schwann cells, and Schwannoma cells // J Neurosci Res. 1999. Vol. 57, N 2. P. 166–175. doi: 10.1002/(SICI)1097-4547(19990715)57:2&lt;166::AID-JNR2&gt;3.0.CO;2-Y</mixed-citation></citation-alternatives></ref></ref-list></back></article>
