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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="research-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Russian Journal of Physiology</journal-id><journal-title-group><journal-title xml:lang="en">Russian Journal of Physiology</journal-title><trans-title-group xml:lang="ru"><trans-title>Российский физиологический журнал им. И.М. Сеченова</trans-title></trans-title-group></journal-title-group><issn publication-format="print">0869-8139</issn><issn publication-format="electronic">2658-655X</issn><publisher><publisher-name xml:lang="en">The Russian Academy of Sciences</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">691426</article-id><article-id pub-id-type="doi">10.7868/S2658655X25070017</article-id><article-id pub-id-type="edn">mvgldi</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>REVIEW</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ОБЗОРНЫЕ СТАТЬИ</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">Modern concepts of endoneurial fibroblasts</article-title><trans-title-group xml:lang="ru"><trans-title>Современные представления о фибробластах эндоневрия</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Petrova</surname><given-names>E. S.</given-names></name><name xml:lang="ru"><surname>Петрова</surname><given-names>Е. С.</given-names></name></name-alternatives><email>iempes@yandex.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Kolos</surname><given-names>E. A.</given-names></name><name xml:lang="ru"><surname>Колос</surname><given-names>Е. А.</given-names></name></name-alternatives><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="pub" iso-8601-date="2025-07-15" publication-format="electronic"><day>15</day><month>07</month><year>2025</year></pub-date><volume>111</volume><issue>7</issue><issue-title xml:lang="en">VOL 111, NO7 (2025)</issue-title><issue-title xml:lang="ru">ТОМ 111, №7 (2025)</issue-title><fpage>995</fpage><lpage>1017</lpage><history><date date-type="received" iso-8601-date="2025-09-26"><day>26</day><month>09</month><year>2025</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2025, Russian Academy of Sciences</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2025, Российская академия наук</copyright-statement><copyright-year>2025</copyright-year><copyright-holder xml:lang="en">Russian Academy of Sciences</copyright-holder><copyright-holder xml:lang="ru">Российская академия наук</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/" start_date="2025-07-23"/></permissions><self-uri xlink:href="https://journals.eco-vector.com/0869-8139/article/view/691426">https://journals.eco-vector.com/0869-8139/article/view/691426</self-uri><abstract xml:lang="en"><p>The purpose of this review was to summarize modern concepts of endoneurial fibroblasts of peripheral nerves and their role in reparative nerve regeneration. Along with Schwann cells and macrophages, fibroblasts are the main functionally significant cells of the endoneurium. There is little information in the literature on the characteristics of fibroblasts and their role in the regeneration of damaged nerves. Recent data on the morphofunctional features of endoneurial fibroblasts, their origin in ontogenesis and their functions are presented in the review. The characteristics of immunohistochemical markers used for their identification are presented. The necessity of studying the interactions of fibroblasts with other nerve cells is emphasized to clarify their role in nerve regeneration after injury.</p></abstract><trans-abstract xml:lang="ru"><p>Целью настоящего обзора явилось обобщение современных представлений о фибробластах эндоневрия периферических нервных проводников и их роли в репаративной регенерации нерва. Наряду со шванновскими клетками и макрофагами фибробласты являются основными по функциональной значимости клетками эндоневрия. В литературе имеется мало сведений об особенностях фибробластов и их роли в регенерации поврежденных нервных проводников. В обзоре представлены данные последних лет о морфофункциональных особенностях фибробластов эндоневрия, их происхождении в онтогенезе и их функциях. Дана характеристика иммуногистохимических маркеров, используемых для их идентификации. Подчеркивается необходимость исследования взаимодействий фибробластов с другими клетками нерва для выяснения их роли в регенерации нервных проводников после повреждения.</p></trans-abstract><kwd-group xml:lang="en"><kwd>nerve</kwd><kwd>endoneurium</kwd><kwd>fibroblasts</kwd><kwd>regeneration</kwd><kwd>immunohistochemistry</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>нерв</kwd><kwd>эндоневрий</kwd><kwd>фибробласты</kwd><kwd>регенерация</kwd><kwd>иммуногистохимия</kwd></kwd-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Zochodne DW (2008) Neurobiology of peripheral nerveregeneration. Cambridge, New York, Melbourne, Madrid, Cape Town, Singapore, Sao Paulo: Cambridge Univer Press.</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Одинак ММ, Живолупов СА (2009) Заболевания и травмы периферической нервной системы (обобщение клинического и экспериментального опыта): руководство для врачей. СПб. СпецЛит. [Odinak MM, Zhivolupov SA (2009) Diseases and injuries of the peripheral nervous system (summary of clinical and experimental experience): a guide for doctors. St. Petersburg: SpetsLit. (In Russ)].</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>Wang ML, Rivlin M, Graham JG, Beredjiklian PK (2019) Peripheral nerve injury, scarring, and recovery. Connective Tissue Res 60(1): 3–9. https://doi.org/10.1080/03008207.2018.1489381</mixed-citation></ref><ref id="B4"><label>4.</label><mixed-citation>Madduri S, Gander B (2010) Schwann cell delivery of neurotrophic factors for peripheral nerve regeneration. J Peripher Nerv Syst 15(2): 93–103. https://doi.org/10.1111/j.1529-8027.2010.00257.x</mixed-citation></ref><ref id="B5"><label>5.</label><mixed-citation>Raginov IS, Chelyshev YA (2001) Sensory neurons and Schwann cells during pharmacological stimulation of a regenerating nerve. Neurosci Behav Physiol 31(6): 629–633. https://doi.org/10.1023/a:1012329429655</mixed-citation></ref><ref id="B6"><label>6.</label><mixed-citation>Gomez-Sanchez JA, Carty L, Iruarrizaga-Lejarreta M, Palomo-Irigoyen M, Varela-Rey M, Griffith M, Hantke J, Macias-Camara N, Azkargorta M, Aurrekoetxea I, De Juan VG, Jefferies HB, Aspichueta P, Elortza F, Aransay AM, Martínez-Chantar ML, Baas F, Mato JM, Mirsky R, Woodhoo A, Jessen KR (2015) Schwann cell autophagy, myelinophagy, initiates myelin clearance from injured nerves. J Cell Biol 210(1): 153–168. https://doi.org/10.1083/jcb.201503019</mixed-citation></ref><ref id="B7"><label>7.</label><mixed-citation>Carr MJ, Johnston AP (2017) Schwann cells as drivers of tissue repair and regeneration. Curr Opin Neurobiol 47: 52–57. https://doi.org/10.1016/j.conb.2017.09.003.gomes</mixed-citation></ref><ref id="B8"><label>8.</label><mixed-citation>Petrova ES (2019) Current views on Schwann cells: devel-opment, plasticity, functions. J Evol Biochem Phys 55: 433–447. https://doi.org/10.1134/S0022093019060012</mixed-citation></ref><ref id="B9"><label>9.</label><mixed-citation>Qu WR, Zhu Z, Liu J, Song DB, Tian H, Chen BP, Li R, Deng LX (2021) Interaction between Schwann cells and other cells during repair of peripheral nerve injury. Neural Regen Res 16(1): 93–98. https://doi.org/10.4103/1673-5374.286956</mixed-citation></ref><ref id="B10"><label>10.</label><mixed-citation>Челышев ЮА, Сайткулов КИ (2000) Развитие, фенотипическая характеристика и коммуникации шванновских клеток. Успехи физиол наук 31(3): 54–69. [Chelyshev YuA, Saitkulov KI (2000) Development, pheno-typic characteristics and communication of Schwanncells. Uspekhi fiziol nauk 31(3): 54–69. (In Russ)].</mixed-citation></ref><ref id="B11"><label>11.</label><mixed-citation>Mirsky R, Jessen KR, Brennan A, Parkinson D, Dong Z, Meier C, Parmantier E, Lawson D (2002) Schwann cells as regulators of nerve development. J Physiol Paris 96(1-2): 17–24. https://doi.org/10.1016/s0928-4257(01)00076-6</mixed-citation></ref><ref id="B12"><label>12.</label><mixed-citation>Bhatheja K, Field J (2006) Schwann cells: origins and role in axonal maintenance and regeneration. Int J Biochem Cell Biol 38: 1995–1999. https://doi.org/10.1016/j.biocel.2006.05.007</mixed-citation></ref><ref id="B13"><label>13.</label><mixed-citation>Griffin JW, Thompson WJ (2008) Biology and pathology of nonmyelinating Schwann cells. Glia 56(14): 1518–1531. https://doi.org/10.1002/glia.20778</mixed-citation></ref><ref id="B14"><label>14.</label><mixed-citation>Kastriti ME, Adameyko I (2017) Specification, plasticity and evolutionary origin of peripheral glial cells. Curr Opin Neurobiol 47: 196–202. https://doi.org/10.1016/j.conb.2017.11.004</mixed-citation></ref><ref id="B15"><label>15.</label><mixed-citation>Bosch-Queralt M, Fledrich R, Stassart RM (2023) Schwann cell functions in peripheral nerve development and repair. Neurobiol Dis 176: 105952. https://doi.org/10.1016/j.nbd.2022.105952</mixed-citation></ref><ref id="B16"><label>16.</label><mixed-citation>Stassart RM, Gomez-Sanchez JA, Lloyd AC (2014) Schwann cells as orchestrators of nerve repair: implications for tissue regeneration and pathologies. Cold Spring Harb Perspect Biol 16(6): a041363. https://doi.org/10.1101/cshperspect.a041363</mixed-citation></ref><ref id="B17"><label>17.</label><mixed-citation>Pinã-Oviedo S, Ortiz-Hidalgo C (2008) The normal and neoplastic perineurium. A review. Adv Anat Pathol 15: 147–164. https://doi.org/10.1097/PAP.0b013e31816f8519</mixed-citation></ref><ref id="B18"><label>18.</label><mixed-citation>Piña AR, Martínez MM, de Almeida OP (2015) Glut-1, best immunohistochemical marker for perineurial cells. Head Neck Pathol 9(1): 104–106. https://doi.org/10.1007/s12105-014-0544-6</mixed-citation></ref><ref id="B19"><label>19.</label><mixed-citation>Petrova ES, Kolos EA (2022) Current views on perineurial cells: unique origin, structure, functions. J Evol Biochem Physiol 58(1): 1–23. https://doi.org/10.1134/S002209302201001X</mixed-citation></ref><ref id="B20"><label>20.</label><mixed-citation>Mueller M, Wacker K, Ringelstein EB, Hickey WF, Imai Y, Kiefer R (2001) Rapid response of identified resident endoneurial macrophages to nerve injury. Am J Pathol 159(6): 2187–2197. https://doi.org/10.1016/S0002-9440(10)63070-2</mixed-citation></ref><ref id="B21"><label>21.</label><mixed-citation>Griffin JW, George R, Ho T (1993) Macrophage systems in peripheral nerves. A review. J Neuropathol Exp Neurol 52(6): 553–560. https://doi.org/10.1097/00005072-199311000-00001</mixed-citation></ref><ref id="B22"><label>22.</label><mixed-citation>Петрова ЕС, Колос ЕА (2024) Изучение резидентных макрофагов эндоневрия седалищного нерва крысы. Матер VI Нац конгр регенерат мед СПб. Эко-Вектор. 764–765. [Petrova ES, Kolos EA (2024) Study of resident macrophages in the endoneurium of the rat sciatic nerve. Mater VI Nac Kongr Regenerat Med SPb. Eko-Vektor. 764–765. (In Russ)]. https://doi.org/10.17816/morph.konf2024</mixed-citation></ref><ref id="B23"><label>23.</label><mixed-citation>Richard L, Topilko P, Magy L, Decouvelaere AV, Charnay P, Funalot B, Vallat JM (2012) Endoneurial fibroblast-like cells. J Neuropathol Exp Neurol 71: 938–947. https://doi.org/10.1097/NEN.0b013e318270a941</mixed-citation></ref><ref id="B24"><label>24.</label><mixed-citation>Ноздрачев АД, Чумасов ЕИ (1999) Периферическая нервная система. СПб. Наука. [Nozdrachev AD, Chumasov EI (1999) Peripheral nervous system. SPb. Nauka. (In Russ)].</mixed-citation></ref><ref id="B25"><label>25.</label><mixed-citation>Kucenas S (2015) Perineurial glia. Cold Spring Harb Perspect Biol 7(6): a020511. https://doi.org/10.1101/cshperspect.a020511</mixed-citation></ref><ref id="B26"><label>26.</label><mixed-citation>Ren Z, Tan Y, Zhao L (2024) Cell heterogeneity and variability in peripheral nerve after injury. Int J Mol Sci 25: 3511. https://doi.org/10.3390/ijms25063511</mixed-citation></ref><ref id="B27"><label>27.</label><mixed-citation>Yim AKY, Wang PL, Bermingham JR Jr, Hackett A, Strickland A, Miller TM, Ly C, Mitra RD, Milbrandt J (2022) Disentangling glial diversity in peripheral nerves at single-nuclei resolution. Nat Neurosci 25: 238–251. https://doi.org/10.1038/s41593-021-01005-1</mixed-citation></ref><ref id="B28"><label>28.</label><mixed-citation>Carr MJ, Toma JS, Johnston APW, Steadman PE, Yuzwa SA, Mahmud N, Frankland PW, Kaplan DR, Miller FD (2019) Mesenchymal precursor cells in adult nerves contribute to mammalian tissue repair and regeneration. Cell Stem Cell 24: 240–256.e9. https://doi.org/10.1016/j.stem.2018.10.024</mixed-citation></ref><ref id="B29"><label>29.</label><mixed-citation>Chen B, Banton MC, Singh L, Parkinson DB, Dun XP (2021) Single cell transcriptome data analysis defines the heterogeneity of peripheral nerve cells in homeostasis and regeneration. Front Cell Neurosci 15: 624826. https://doi.org/10.3389/fncel.2021.624826</mixed-citation></ref><ref id="B30"><label>30.</label><mixed-citation>Zotter B, Dagan O, Brady J, Baloui H, Samanta J, Salzer JL (2022) Gli1 regulates the postnatal acquisition of peripheral nerve architecture. J Neurosci 42(2): 183–201. https://doi.org/10.1523/JNEUROSCI.3096-20.2021</mixed-citation></ref><ref id="B31"><label>31.</label><mixed-citation>Richard L, Védrenne N, Vallat JM, Funalot B (2014) Characterization of endoneurial fibroblast-like cells from human and rat peripheral nerves. J Histochem Cytochem 62(6): 424–435. https://doi.org/10.1369/0022155414530994</mixed-citation></ref><ref id="B32"><label>32.</label><mixed-citation>Ramon y Cahal S (1928) Degeneration and regeneration of the nervous system. V 1–2. L. Oxf. H. Milford.</mixed-citation></ref><ref id="B33"><label>33.</label><mixed-citation>Nageotte J, Guyon L (1930) Reticulin. Am J Pathol 6(6): 631–654.5.</mixed-citation></ref><ref id="B34"><label>34.</label><mixed-citation>Sorrell JM, Caplan AI (2009) Fibroblasts-a diverse population at the center of it all. Int Rev Cell Mol Biol 276: 161–214. https://doi.org/10.1016/S1937-6448(09)76004-6</mixed-citation></ref><ref id="B35"><label>35.</label><mixed-citation>Laidlaw GF (1930) Silver Staining of the Endoneurial Fibers of the Cerebrospinal Nerves. Am J Pathol 6(4): 435–444.3.</mixed-citation></ref><ref id="B36"><label>36.</label><mixed-citation>Joseph NM, Mukouyama YS, Mosher JT, Jaegle M, Crone SA, Dormand EL, Lee KF, Meijer D, Anderson DJ, Morrison SJ (2004) Neural crest stem cells undergo multilineage differentiation in developing peripheral nerves to generate endoneurial fibroblasts in addition to Schwann cells. Development 131: 5599–5612. https://doi.org/10.1242/dev.01429</mixed-citation></ref><ref id="B37"><label>37.</label><mixed-citation>Le Lièvre CS, Le Douarin NM (1975) Mesenchymal derivatives of the neural crest: analysis of chimaeric quail and chick embryos. J Embryol Exp Morphol 34(1): 125–154.</mixed-citation></ref><ref id="B38"><label>38.</label><mixed-citation>Le Douarin NM, Dupin E (2018) The "beginnings" of the neural crest. Dev Biol 444(1): 3–13. https://doi.org/10.1016/j.ydbio.2018.07.019</mixed-citation></ref><ref id="B39"><label>39.</label><mixed-citation>Пахомова НЮ, Строкова ЕЛ, Корыткин АА, Кожевников ВВ, Гусев АФ, Зайдман АМ (2023) История изучения нервного гребня (обзор). Сибирск научн мед журн 43(1): 13–29. [Pakhomova NY, Strokova EL, Korytkin AA, Kozhevnikov VV, Gusev AF, Zaidman AM (2023) The History of the Study of the Neural Crest (Overview). Sibirsk nauchn med zhurn 43(1): 13–29. (In Russ)]. https://doi.org/10.18699/SSMJ20230102</mixed-citation></ref><ref id="B40"><label>40.</label><mixed-citation>Woodhoo A, Sommer L (2008) Development of the Schwann cell lineage: From the neural crest to the myelinated nerve. Glia 56: 1481–1490. https://doi.org/10.1002/glia.20723</mixed-citation></ref><ref id="B41"><label>41.</label><mixed-citation>Furlan A, Adameyko I (2018) Schwann cell precursor: a neural crest cell in disguise? Dev Biol 444(1): 25–35. https://doi.org/10.1016/j.ydbio.2018.02.008</mixed-citation></ref><ref id="B42"><label>42.</label><mixed-citation>Kastriti ME, Faure L, von Ahsen D, Bouderlique TG, Bostrom J, Solovieva T, Jackson C, Bronner M, Meijer D, Hadjab S, Lallemend F, Erickson A, Kaucka M, Dyachuk V, Perlmann T, Lahti L, Krivanek J, Brunet J, Fried K, Adameyko I (2022) Schwann cell precursors represent a neural crest-like state with biased multipotency. EMBO J 41(17): e108780. https://doi.org / 10.15252/embj.2021108780</mixed-citation></ref><ref id="B43"><label>43.</label><mixed-citation>Mirancea N (2016) Telocyte – a particular cell phenotype. Infrastructure, relationships and putative functions. Rom J Morphol Embryol 57(1): 7–21.</mixed-citation></ref><ref id="B44"><label>44.</label><mixed-citation>Mirancea N, Mirancea GV, Moroşanu AM (2022) Telocytes inside of the peripheral nervous system – a 3D endoneurial network and putative role in cell communication. Rom J Morphol Embryol 63(2): 335–347. https://doi.org/10.47162/RJME.63.2.05</mixed-citation></ref><ref id="B45"><label>45.</label><mixed-citation>Díaz-Flores L, Gutiérrez R, García MP, Gayoso S, Gutiérrez E, Díaz-Flores L Jr, Carrasco JL (2020) Telocytes in the Normal and Pathological Peripheral Nervous System. Int J Mol Sci 21(12): 4320. https://doi.org/10.3390/ijms21124320</mixed-citation></ref><ref id="B46"><label>46.</label><mixed-citation>Popescu LM, Faussone-Pellegrini MS (2010) Telocytes – a case of serendipity: the winding way from interstitial cells of Cajal (ICC), via Interstitial Cajal-Like Cells (ICLC) to telocytes. J Cell Mol Med 14(4): 729–740. https://doi.org/10.1111/j.1582-4934.2010.01059.x</mixed-citation></ref><ref id="B47"><label>47.</label><mixed-citation>Faussone Pellegrini MS, Popescu LM (2011) Telocytes. Biomol Concepts 2(6): 481–489. https://doi.org/10.1515/BMC.2011.039</mixed-citation></ref><ref id="B48"><label>48.</label><mixed-citation>Низяева НВ, Марей МВ, Сухих ГТ, Щёголев АИ (2014) Интерстициальные пейсмейкерные клетки. Вестн Рос акад мед наук 69(7-8): 17–24. [Nizyaeva NV, Marej MV, Sukhikh GT, Shchyogolev AI (2014) Interstitial pacemaker cells. Vestn Ross akad med nauk 69(7-8): 17–24. (In Russ)]. https://doi.org/10.15690/vramn.v69i7-8.1105</mixed-citation></ref><ref id="B49"><label>49.</label><mixed-citation>Одинцова ИА, Слуцкая ДР, Березовская ТИ (2022) Телоциты: локализация, структура, функции и значение в патологии. Гены и Клетки 17(1): 6–12. [Odincova IA, Sluckaya DR, Berezovskaya TI (2022) Telocytes: localization, structure, functions and significance in pathology. Geny i Kletki 17(1): 6–12. (In Russ)]. https://doi.org/10.23868/202205001</mixed-citation></ref><ref id="B50"><label>50.</label><mixed-citation>Chen T, Li Y, Ni W, Wei Y, Li J, Yu J, Zhang L, Gao J, Zhou J, Zhang W, Xu H, Hu J (2020) Neural stem cell-conditioned medium inhibits inflammation in macrophages via Sirt-1 signaling pathway in vitro and promotes sciatic nerve injury recovery. Stem Cells and Develop https://doi.org/10.1089/scd.2020.0020</mixed-citation></ref><ref id="B51"><label>51.</label><mixed-citation>Petrova ES, Kolos EA (2023) Immunohistochemical Study of Macrophages of Sciatic Rat Nerve after Damage and Subperineural Injection of Mesenchymal Stem Cells. Russ Physiol J 109(4): 466–476 (In Russ). https://doi.org/10.31857/S0869813923040076</mixed-citation></ref><ref id="B52"><label>52.</label><mixed-citation>Трусов ГА, Чапленко АА, Семенова ИС, Мельникова ЕВ, Олефир ЮВ (2018) Применение проточной цитометрии для оценки качества биомедицинских клеточных продуктов. БИОпрепараты. Профилактика, диагностика, лечение 18(1): 16–24. [Trusov GA, Chaplenko AA, Semenova IS, Mel'nikova EV, Olefir YuV (2018) Application of flow cytometry for quality assessment of biomedical cell products. BIOpreparaty. Profilaktika, diagnostika, lechenie 18(1): 16–24. (In Russ)]. https://doi.org/10.30895/2221-996KH-2018-18-1-16-24</mixed-citation></ref><ref id="B53"><label>53.</label><mixed-citation>Lupatov AY, Vdovin AS, Vakhrushev IV, Poltavtseva RA, Yarygin KN (2015) Comparative analysis of the expression of surface markers on fibroblasts and fibroblast-like cells isolated from different human tissues. Bull Exp Biol Med 158(4): 537–543. https://doi.org/10.1007/s10517-015-2803-2</mixed-citation></ref><ref id="B54"><label>54.</label><mixed-citation>Hill R (2009). Extracellular matrix remodelling in human diabetic neuropathy. J Anat 214: 219–225. https://doi.org/10.1111/j.1469-7580.2008.01026.x</mixed-citation></ref><ref id="B55"><label>55.</label><mixed-citation>Yamamoto M, Okui N, Tatebe M, Shinohara T, Hirata H (2011) Regeneration of the perineurium after microsurgical resection examined with immunolabeling for tenascin-C and alpha smooth muscle actin. J Anat 218: 413–425. https://doi.org/10.1111/j.1469-7580.2011.01341.x</mixed-citation></ref><ref id="B56"><label>56.</label><mixed-citation>Rotshenker S (2011) Wallerian degeneration: the innate-immune response to traumatic nerve injury. J Neuroinflammat 8: 109. https://doi.org/10.1186/1742-2094-8-109</mixed-citation></ref><ref id="B57"><label>57.</label><mixed-citation>Колос ЕА (2023) Коннексин-43 в клетках регенерирующего седалищного нерва крысы. Морфология 161(3): 71–78. [Kolos EA (2023) Connexin-43 in regenerating rat sciatic nerve cells. Morfologiya 161(3): 71–78. (In Russ)]. https://doi.org/10.17816/morph.629037</mixed-citation></ref><ref id="B58"><label>58.</label><mixed-citation>Civin CI, Almeida-Porada G, Lee MJ, Olweus J, Terstappen LW, Zanjani ED (1996) Sustained, retransplantable, multilineage engraftment of highly purified adult human bone marrow stem cells in vivo. Blood 88(11): 4102–4109. https://doi.org/10.1182/blood.V88.11.4102.4102</mixed-citation></ref><ref id="B59"><label>59.</label><mixed-citation>Smeland EB, Funderud S, Kvalheim G, Gaudernack G, Rasmussen AM, Rusten L, Wang MW, Tindle RW, Blomhoff HK, Egeland T (1992) Isolation and characterization of human hematopoietic progenitor cells: an effective method for positive selection of CD34+ cells. Leukemia 6(8): 845–852.</mixed-citation></ref><ref id="B60"><label>60.</label><mixed-citation>He Q, Yu F, Li Y, Sun J, Ding F (2020) Purification of fibroblasts and schwann cells from sensory and motor nerves in vitro. J Vis Exp 159: e60952. https://doi.org/10.3791/60952</mixed-citation></ref><ref id="B61"><label>61.</label><mixed-citation>Levine JM, Nishiyama A (1996) The NG2 chondroitin sulfate proteoglycan: a multifunctional proteoglycan associated with immature cells. Perspect Dev Neurobiol 3(4): 245–259.</mixed-citation></ref><ref id="B62"><label>62.</label><mixed-citation>Levine JM (1994) Increased expression of the NG2 chondroitin-sulfate proteoglycan after brain injury. J Neurosci 14(8): 4716–4730. https://doi.org/10.1523/JNEUROSCI.14-08-04716.1994</mixed-citation></ref><ref id="B63"><label>63.</label><mixed-citation>Chiquet-Ehrismann R (2004) Tenascins. Int J Biochem Cell Biol 36(6): 986–990. https://doi.org/10.1016/j.biocel.2003.12.002</mixed-citation></ref><ref id="B64"><label>64.</label><mixed-citation>Peng K, Sant D, Andersen N, Silvera R, Camarena V, Piñero G, Graham R, Khan A, Xu XM, Wang G, Monje PV (2020) Magnetic separation of peripheral nerve-resident cells underscores key molecular features of human Schwann cells and fibroblasts: an immunochemical and transcriptomics approach. Sci Rep 10(1): 18433. https://doi.org/10.1038/s41598-020-74128-3</mixed-citation></ref><ref id="B65"><label>65.</label><mixed-citation>Fertala J, Rivlin M, Wang ML, Beredjiklian PK, Steplewski A, Fertala A (2020) Collagen-rich deposit formation in the sciatic nerve after injury and surgical repair: A study of collagen-producing cells in a rabbit model. Brain Behav 10(10): e01802. https://doi.org/10.1002/brb3.1802</mixed-citation></ref><ref id="B66"><label>66.</label><mixed-citation>Du H, Chen D, Zhou Y, Han Z, Che G (2014) Fibroblast phenotypes in different lung diseases. J Cardiothorac Surg 9: 147. https://doi.org/10.1186/s13019-014-0147-z</mixed-citation></ref><ref id="B67"><label>67.</label><mixed-citation>Лунина НА, Сафина ДР, Костровa СВ (2023) Ассоциированные с опухолью фибробласты: гетерогенность и бимодальность в онкогенезе. Мол биол 57(5): 739–770. [Lunina NA, Safina DR, Kostrov SV (2023) Cancer-Associated Fibroblasts: Heterogeneity and Bimodality in Oncogenesis. Mol Biol 57(5): 739–770. (In Russ)]. https://doi.org/10.31857/S0026898423050105</mixed-citation></ref><ref id="B68"><label>68.</label><mixed-citation>Kolarcik CL, Catt K, Rost E, Albrecht IN, Bourbeau D, Du Z, Kozai TD, Luo X, Weber DJ, Cui XT (2015) Evaluation of poly(3,4-ethylenedioxythiophene)/carbon nanotube neural electrode coatings for stimulation in the dorsal root ganglion. J Neural Eng 12(1): 016008. https://doi.org/10.1088/1741-2560/12/1/016008</mixed-citation></ref><ref id="B69"><label>69.</label><mixed-citation>Kolarcik CL, Castro CA, Lesniak A, Demetris AJ, Fisher LE, Gaunt RA, Weber DJ, Cui XT (2020) Host tissue response to floating microelectrode arrays chronically implanted in the feline spinal nerve. J Neural Eng 17(4): 046012. https://doi.org/10.1088/1741-2552/ab94d7</mixed-citation></ref><ref id="B70"><label>70.</label><mixed-citation>Nissi R, Autio-Harmainen H, Marttila P, Sormunen R, Kivirikko KI (2001) Prolyl 4-hydroxylase isoenzymes I and II have different expression patterns in several human tissues. J Histochem Cytochem 49(9): 1143–1153. https://doi.org/10.1177/002215540104900908</mixed-citation></ref><ref id="B71"><label>71.</label><mixed-citation>Sato H, Ishii Y, Yamamoto S, Azuma E, Takahashi Y, Hamashima T, Umezawa A, Mori H, Kuroda S, Endo S, Sasahara M (2016) PDGFR-β plays a key role in the ectopic migration of neuroblasts in cerebral stroke. Stem Cells 34(3): 685–698. https://doi.org/10.1002/stem.2212</mixed-citation></ref><ref id="B72"><label>72.</label><mixed-citation>Zhou C, Liu B, Huang Y, Zeng X, You H, Li J, Zhang Y (2017) The effect of four types of artificial nerve graft structures on the repair of 10-mm rat sciatic nerve gap. J Biomed Mater Res A 105(11): 3077–3085. https://doi.org/10.1002/jbm.a.36172</mixed-citation></ref><ref id="B73"><label>73.</label><mixed-citation>Hamidi H, Ivaska J (2017) Vascular morphogenesis: an integrin and fibronectin highway. Curr Biol 27(4): R158–R161. https://doi.org/10.1016/j.cub.2016.12.036</mixed-citation></ref><ref id="B74"><label>74.</label><mixed-citation>Zent J, Guo LW (2018) Signaling mechanisms of myofibroblastic activation: outside-in and inside-out. Cell Physiol Biochem 49(3): 848–868. https://doi.org/10.1159/000493217</mixed-citation></ref><ref id="B75"><label>75.</label><mixed-citation>Mohammadizadeh F, Heydari S (2020) Intracellular fibronectin expression in invasive breast carcinoma: is it related to significant clinicopathological hrognostic factors? Iran Red Crescent Med J 22(4): e98676. https://doi.org/10.5812/ircmj.98676</mixed-citation></ref><ref id="B76"><label>76.</label><mixed-citation>Darby IA, Hewitson TD (2007) Fibroblast differentiation in wound healing and fibrosis. Int Rev Cytol 257: 143–179. https://doi.org/10.1016/S0074-7696(07)57004-X</mixed-citation></ref><ref id="B77"><label>77.</label><mixed-citation>Хлопин НГ (1946) Общебиологические и экспериментальные основы гистологии. М. Изд-во Акад наук СССР. [Hlopin NG (1946) General biological and experimental principles of histology. M. Izd-vo Akad nauk SSSR. (In Russ)].</mixed-citation></ref><ref id="B78"><label>78.</label><mixed-citation>Михайлов ВП (1972) Классификация тканей и явления метоплазии в свете принципа тканевой детерминации. Архив анатом гистол эмбриол 63(6): 12–33. [Mihajlov VP (1972) Classification of tissues and phenomena of metaplasia in terms of the principle of tissue determination. Arhiv anatom gistol embriol 63(6): 12–33. (In Russ)].</mixed-citation></ref><ref id="B79"><label>79.</label><mixed-citation>Raff MC, Fields KL, Hakomori SI, Mirsky R, Pruss RM, Winter J (1979) Cell-type-specific markers for distinguishing and studying neurons and the major classes of glial cells in culture. Brain Res 174(2): 283–308. https://doi.org/10.1016/0006-8993(79)90851-5</mixed-citation></ref><ref id="B80"><label>80.</label><mixed-citation>Faniku C, Kong W, He L, Zhang M, Lilly G, Pepper JP (2021) Hedgehog signaling promotes endoneurial fibroblast migration and Vegf-A expression following facial nerve injury. Brain Res 1751: 147204. https://doi.org/10.1016/j.brainres.2020.147204</mixed-citation></ref><ref id="B81"><label>81.</label><mixed-citation>Tricaud N, Park HT (2017) Wallerian demyelination: chronicle of a cellular cataclysm. Cell Mol Life Sci 74 (22): 4049–4057. https://doi.org/10.1007/s00018-017-2565-2</mixed-citation></ref><ref id="B82"><label>82.</label><mixed-citation>Zigmond RE, Echevarria FD (2019) Macrophage biology in the peripheral nervous system after injury. Prog Neurobiol 173: 102–121. https://doi.org/10.1016/j.pneurobio.2018.12.001</mixed-citation></ref><ref id="B83"><label>83.</label><mixed-citation>Kolter J, Kierdorf K, Henneke P (2020) Origin and Differentiation of Nerve-Associated Macrophages. J Immunol 204(2): 271–279. https://doi.org/10.4049/jimmunol.1901077</mixed-citation></ref><ref id="B84"><label>84.</label><mixed-citation>Zhang Z, Yu B, Gu Y, Zhou S, Qian T, Wang Y, Ding G, Ding F, Gu X (2016) Fibroblast-derived tenascin-C promotes Schwann cell migration through beta1-integrin dependent pathway during peripheral nerve regeneration. Glia 64(3): 374–385. https://doi.org/10.1002/glia.22934</mixed-citation></ref><ref id="B85"><label>85.</label><mixed-citation>Dun XP, Parkinson DB (2020) Classic axon guidance molecules control correct nerve bridge tissue formation and precise axon regeneration. Neural Regen Res 15(1): 6–9. https://doi.org/10.4103/1673-5374.264441</mixed-citation></ref><ref id="B86"><label>86.</label><mixed-citation>McDonald D, Cheng C, Chen Y, Zochodne D (2006) Early events of peripheral nerve regeneration. Neuron Glia Biol 2: 139–147. https://doi.org/10.1017/S1740925X05000347</mixed-citation></ref><ref id="B87"><label>87.</label><mixed-citation>Lemke G (2006) Neuregulin-1 and myelination. Sci STKE 325: pe11. https://doi.org/10.1126/stke.3252006pe11</mixed-citation></ref><ref id="B88"><label>88.</label><mixed-citation>Fornasari BE, El Soury M, Nato G, Fucini A, Carta G, Ronchi G, Crosio A, Perroteau I, Geuna S, Raimondo S, Gambarotta G (2020) Fibroblasts colonizing nerve conduits express high levels of soluble neuregulin1, a factor promoting Schwann cell dedifferentiation. Cells 9(6): 1366. https://doi.org/10.3390/cells9061366</mixed-citation></ref><ref id="B89"><label>89.</label><mixed-citation>Saada A, Dunaevsky-Hutt A, Aamar A, Reichert F, Rotshenker S (1995) Fibroblasts that reside in mouse and frog injured peripheral nerves produce apolipoproteins. J Neurochem 64: 1996–2003. https://doi.org/10.1046/j.1471-4159.1995.64051996.x</mixed-citation></ref><ref id="B90"><label>90.</label><mixed-citation>Ельчанинов АВ, Фатхудинов ТХ (2023) Макрофаги. Москва. ГЭОТАР-Медиа. [El`chaninov AV, Fatxudinov TX (2023) Macrophages. Moskva. GE`OTAR-Media. (In Russ)]. https://doi.org/10.33029/9704-7780-9-EAM-2023-1-208)</mixed-citation></ref><ref id="B91"><label>91.</label><mixed-citation>Chen P, Piao X, Bonaldo P (2015) Role of macrophages in Wallerian degeneration and axonal regeneration after peripheral nerve injury. Acta Neuropathol 130(5): 605–618. https://doi.org/10.1007/s00401-015-1482-4</mixed-citation></ref><ref id="B92"><label>92.</label><mixed-citation>Heumann R, Korsching S, Bandtlow C, Thoenen H (1987) Changes of nerve growth factor synthesis in nonneuronal cells in response to sciatic nerve transection. J Cell Biol 104: 1623–1631. https://doi.org/10.1083/jcb.104.6.1623</mixed-citation></ref><ref id="B93"><label>93.</label><mixed-citation>Зорина АИ, Бозо ИЯ, Зорин ВЛ, Черкасов ВР, Деев РВ (2011) Фибробласты дермы: особенности цитогенеза, цитофизиологии и возможности клинического применения. Клеточн трансплантол тканев инженер 6(2): 15–26. [Zorina AI, Bozo IYa, Zorin VL, Cherkasov VR, Deev RV (2011) Dermal fibroblasts: features of cytogenesis, cytophysiology and possibilities of clinical application. Kletochn transplantol tkanev inzhener 6(2): 15–26. (In Russ)].</mixed-citation></ref><ref id="B94"><label>94.</label><mixed-citation>Zhao Y, Liang Y, Xu Z, Liu J, Liu X, Ma J, Sun C, Yang Y (2022) Exosomal miR-673-5p from fibroblasts promotes Schwann cell-mediated peripheral neuron myelination by targeting the TSC2/mTORC1/SREBP2 axis. J Biol Chem 298(3): 101718. https://doi.org/10.1016/j.jbc.2022.101718</mixed-citation></ref><ref id="B95"><label>95.</label><mixed-citation>Bunge MB, Wood PM, Tynan LB, Bates ML, Sanes JR (1989) Perineurium originates from fibroblasts: demonstration in vitro with a retroviral marker. Science 243(4888): 229–231. https://doi.org/10.1126/science.2492115</mixed-citation></ref><ref id="B96"><label>96.</label><mixed-citation>Hou H, Zhang L, Ye Z, Li J, Lian Z, Chen C, He R, Peng B, Xu Q, Zhang G, Gan W, Tang P (2016) Chitooligosaccharide inhibits scar formation and enhances functional recovery in a mouse model of sciatic nerve injury. Mol Neurobiol 53(4): 2249–2257. https://doi.org/10.1007/s12035-015-9196-0</mixed-citation></ref><ref id="B97"><label>97.</label><mixed-citation>Ngeow WC (2010) Scar less: a review of methods of scar reduction at sites of peripheral nerve repair. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 109(3): 357–366. https://doi.org/10.1016/j.tripleo.2009.06.030</mixed-citation></ref><ref id="B98"><label>98.</label><mixed-citation>Порсева ВВ, Преображенский НД, Маслюков ПМ (2023) Экспрессия парвальбумина в ГАД67-иммунореактивных нейронах промежуточной зоны грудного спинного мозга у мышей C57BL/6 в условиях сенсорной денервации. Рос журн боли 21(1): 13–18. [Porseva VV, Preobrazhensky ND, Maslyukov PM (2023) Expression of parvalbumin in GAD67-immunoreactive neurons of the intermediate zone of the thoracic spinal cord in C57BL/6 mice under conditions of sensory denervation. Ross zhurn boli 21(1): 13–18. (In Russ)]. https://doi.org/10.17116/pain20232101113</mixed-citation></ref><ref id="B99"><label>99.</label><mixed-citation>Antunes SLG, Jardim MR, Vital RT, Pascarelli BMO, Nery JADC, Amadeu TP, Sales AM, da Costa EAF, Sarno EN (2019) Fibrosis: a distinguishing feature in the pathology of neural leprosy. Mem Inst Oswaldo Cruz 114: e190056. https://doi.org/10.1590/0074-02760190056</mixed-citation></ref><ref id="B100"><label>100.</label><mixed-citation>Pradat PF, Delanian S (2013) Late radiation injury to peripheral nerves. Handb Clin Neurol 115: 743–758. https://doi.org/10.1016/B978-0-444-52902-2.00043-6</mixed-citation></ref><ref id="B101"><label>101.</label><mixed-citation>Bisceglia M, Vigilante E, Ben-Dor D (2007) Neural lipofibromatous hamartoma: a report of two cases and review of the literature. Adv Anat Pathol 14(1): 46–52. https://doi.org/10.1097/PAP.0b013e31802f04b7</mixed-citation></ref><ref id="B102"><label>102.</label><mixed-citation>Seddon HJ (1942) Classification of Nerve Injuries. Br Med J 2(4260): 237–239. https://doi.org/10.1136/bmj.2.4260.237</mixed-citation></ref><ref id="B103"><label>103.</label><mixed-citation>Sunderland S (1951) A classification of peripheral nerve injuries producing loss of function. Brain. 74(4): 491–516. https://doi.org/10.1093/brain/74.4.491</mixed-citation></ref><ref id="B104"><label>104.</label><mixed-citation>Aman M, Mayrhofer-Schmid M, Schwarz D, Bendszus M, Daeschler SC, Klemm T, Kneser U, Harhaus L, Boecker AH (2023) Avoiding scar tissue formation of peripheral nerves with the help of an acellular collagen matrix. PLoS One 18(8): e0289677. https://doi.org/10.1371/journal.pone.0289677</mixed-citation></ref></ref-list></back></article>
