<?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="other" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Genes &amp; Cells</journal-id><journal-title-group><journal-title xml:lang="en">Genes &amp; Cells</journal-title><trans-title-group xml:lang="ru"><trans-title>Гены и Клетки</trans-title></trans-title-group><trans-title-group xml:lang="zh"><trans-title>Genes and Cells</trans-title></trans-title-group></journal-title-group><issn publication-format="print">2313-1829</issn><issn publication-format="electronic">2500-2562</issn><publisher><publisher-name xml:lang="en">Human Stem Cells Institute</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">121672</article-id><article-id pub-id-type="doi">10.23868/gc121672</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>Articles</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>Статьи</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">Sinusoidal liver cells and bone marrow cells as components of the common functional systemfor regulation of recovery morphogenesis of healthy and damaged liver</article-title><trans-title-group xml:lang="ru"><trans-title>Синусоидальные клетки печени и клетки костного мозгакак компоненты единой функциональной системырегуляции восстановительного морфогенезав здоровой и поврежденной печени</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Onischenko</surname><given-names>N A</given-names></name><name xml:lang="ru"><surname>Онищенко</surname><given-names>Н А</given-names></name></name-alternatives><bio xml:lang="en"><p>V.I. Shumakov Federal Research Center for Transplantology and Artificial Organs, the Ministry of Public Healthand Social Development, Moscow</p></bio><bio xml:lang="ru"><p>ФГУ «ФНЦ Трансплантологии и искусственных органов им. акад. В.И. Шумакова»Минздравсоцразвития, Москва</p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Lyundup</surname><given-names>A V</given-names></name><name xml:lang="ru"><surname>Люндуп</surname><given-names>А В</given-names></name></name-alternatives><bio xml:lang="en"><p>V.I. Shumakov Federal Research Center for Transplantology and Artificial Organs, the Ministry of Public Healthand Social Development, Moscow</p></bio><bio xml:lang="ru"><p>ФГУ «ФНЦ Трансплантологии и искусственных органов им. акад. В.И. Шумакова»Минздравсоцразвития, Москва</p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Deev</surname><given-names>R V</given-names></name><name xml:lang="ru"><surname>Деев</surname><given-names>Р В</given-names></name></name-alternatives><bio xml:lang="en"><p>Human Stem Cells Institute, Moscow</p></bio><bio xml:lang="ru"><p>Институт cтволовых клеток человека, Москва</p></bio><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Shagidulin</surname><given-names>M Y</given-names></name><name xml:lang="ru"><surname>Шагидулин</surname><given-names>М Ю</given-names></name></name-alternatives><bio xml:lang="en"><p>V.I. Shumakov Federal Research Center for Transplantology and Artificial Organs, the Ministry of Public Healthand Social Development, Moscow</p></bio><bio xml:lang="ru"><p>ФГУ «ФНЦ Трансплантологии и искусственных органов им. акад. В.И. Шумакова»Минздравсоцразвития, Москва</p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Krasheninnikov</surname><given-names>M E</given-names></name><name xml:lang="ru"><surname>Крашенинников</surname><given-names>М Е</given-names></name></name-alternatives><bio xml:lang="en"><p>V.I. Shumakov Federal Research Center for Transplantology and Artificial Organs, the Ministry of Public Healthand Social Development, Moscow</p></bio><bio xml:lang="ru"><p>ФГУ «ФНЦ Трансплантологии и искусственных органов им. акад. В.И. Шумакова»Минздравсоцразвития, Москва</p></bio><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">V.I. Shumakov Federal Research Center for Transplantology and Artificial Organs, the Ministry of Public Healthand Social Development, Moscow</institution></aff><aff><institution xml:lang="ru">ФГУ «ФНЦ Трансплантологии и искусственных органов им. акад. В.И. Шумакова»Минздравсоцразвития, Москва</institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">Human Stem Cells Institute, Moscow</institution></aff><aff><institution xml:lang="ru">Институт cтволовых клеток человека, Москва</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2011-06-15" publication-format="electronic"><day>15</day><month>06</month><year>2011</year></pub-date><volume>6</volume><issue>2</issue><issue-title xml:lang="en">NO2 (2011)</issue-title><issue-title xml:lang="ru">№2 (2011)</issue-title><fpage>78</fpage><lpage>92</lpage><history><date date-type="received" iso-8601-date="2023-01-11"><day>11</day><month>01</month><year>2023</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2011, Eco-Vector</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2011, Эко-Вектор</copyright-statement><copyright-year>2011</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/"/></permissions><self-uri xlink:href="https://genescells.ru/2313-1829/article/view/121672">https://genescells.ru/2313-1829/article/view/121672</self-uri><abstract xml:lang="en"><p>This review presents current information about the
cooperative interaction of sinusoidal liver cells and bone marrow
cells at the processes of physiological, reparative and fibrosing
liver regeneration. It is shown that the stem / progenitor cells
of bone marrow (hematopoietic and mesenchymal stromal
cells) supplement regulatory role of liver stem cells (first
of all stellate cells - Ito cells), reduce the seriousness of
inflammation and fibrosis, and thereby normalize the recovery
process of damaged liver regeneration. It is believed that the
use of mesenchymal stromal cells of bone marrow is the most
future forward strategy. However, to form a final opinion on
the regenerative capacity of autologous and allogeneic bone
marrow cells at hepatic failure large-scale double-blind clinical
trials should be carried out.</p></abstract><trans-abstract xml:lang="ru"><p>В обзоре представлены современные сведения о коо-
перативном взаимодействии синусоидальных клеток пече-
ни и клеток костного мозга при осуществлении процессов
физиологической, репаративной и патологической (фибро-
зирующей) регенерации печени. Показано, что стволовые/
прогениторные клетки костного мозга (гемопоэтические
и мультипатентные мезенхимальные стромальные клетки
(ММСК)) восполняют регуляционную роль стволовых кле-
ток печени (прежде всего звездчатых клеток - клеток Ито),
снижают выраженность процессов воспаления и фибрози-
рования и тем самым модулируют процессы восстанови-
тельной регенерации поврежденной печени.
Полагают, что применение ММСК костного мозга яв-
ляется наиболее перспективной стратегией. Однако для
окончательного суждения о регенераторных возможностях
аутологичных и аллогенных клеток костного мозга при пе-
ченочной недостаточности необходимо проводить широко-
масштабные двойные слепые клинические исследования.</p></trans-abstract></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Gennero L., Roos M.A., Sperber K. et al. Pluripotent plasticity of stem cells and liver repopulation. Cell Biochem. Funct. 2010; 28: 178-89.</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Шумаков В.И., Онищенко Н.А. Биологические резервы клеток костного мозга и коррекция органных дисфункций. М.: Лавр; 2009.</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>Маянский Д.Н. Роль стромы печени в патогенезе гепатитов. Вестник АМН СССР 1988; 5: 81-8.</mixed-citation></ref><ref id="B4"><label>4.</label><mixed-citation>Geerts A. History, heterogeneity, developmental biology, and functions of quiescent hepatic stellate cells. Semin. Liver Dis. 2001; 21: 311-35.</mixed-citation></ref><ref id="B5"><label>5.</label><mixed-citation>Щеглев А.И., Мишнев О.Д. Структурно-метаболическая ха- рактеристика синусоидальных клеток печени. Успехи совр. Биол. 1991; 3(1): 73-82.</mixed-citation></ref><ref id="B6"><label>6.</label><mixed-citation>Секамова С.М., Бекетова Т.П. Функциональная морфология печени. В: Серов В.В., Лапиш К.М., редакторы. Морфологическая диагностика заболеваний печени. М.: Медицина 1989;8-36.</mixed-citation></ref><ref id="B7"><label>7.</label><mixed-citation>Friedman S.L. Molecular regulation of hepatic fibrosis, an integrated cellular response to tissue injury. J. Biol. Chem. 2000; 275: 2247-50.</mixed-citation></ref><ref id="B8"><label>8.</label><mixed-citation>Schuppan D., Ruehl M., Somasundaram R. et al. Matrix as modulator of stellate cell and hepatic fibrogenesis. Semin. Liver Dis. 2001; 21: 351-72.</mixed-citation></ref><ref id="B9"><label>9.</label><mixed-citation>Шерлок Ш., Дули Д. Заболевания печени и желчных путей. М.: ГЭОТАР-Медиа; 2002</mixed-citation></ref><ref id="B10"><label>10.</label><mixed-citation>Yurchenco V., Analysis of basement membrane self-assembly and cellular interactions with native and recombinant glycoproteins. Methods Cell Biol. 2002; 69: 111-44.</mixed-citation></ref><ref id="B11"><label>11.</label><mixed-citation>Онищенко Н.А. Регуляция восстановительных процессов в пе- чени в норме и при патологии. В: Шумакова В.И., Онищенко Н.А., редакторы. Лечение печеночной недостаточности методами трансплантации и экстракорпорального подключения печени и других тканей. М.: ВИНИТИ 1994; 76-141.</mixed-citation></ref><ref id="B12"><label>12.</label><mixed-citation>Kim T.H., Mars W.M., Stolz D.B. et al. Extracellular matrix remodeling at the early stages of liver regeneration in the rat. J. Hepatol. 1997; 26: 896-904.</mixed-citation></ref><ref id="B13"><label>13.</label><mixed-citation>Friedman S.L. Hepatic stellate cells: protean, multifunctional and enigmatic cells of liver. Physiol. Rev. 2008; 88: 125-72.</mixed-citation></ref><ref id="B14"><label>14.</label><mixed-citation>Cassiman D., Libbrecht L., Desmet V. et al. Hepatic stellate cell/myofibroblast subpopulations in fibrotic human and rat livers. J. Hepatol. 2002; 36: 200-09.</mixed-citation></ref><ref id="B15"><label>15.</label><mixed-citation>Corpechot C., Barbu V., Wendum D. et al. Hypoxia-induced VEGF and collagen I expressions are associated with angiogenesis and fibrogenesis in experimental cirrhosis. Hepatology 2002; 35: 1010-21</mixed-citation></ref><ref id="B16"><label>16.</label><mixed-citation>Rockey D.C. Vascular mediators in the injured liver. Hepatology 2003; 37: 4-12.</mixed-citation></ref><ref id="B17"><label>17.</label><mixed-citation>Гумерова А.А., Киясов А.П. Могут ли перисинусоидальные клетки быть региональными стволовыми клетками (прогениторны- ми) клетками печени? Клеточная трансплантология и тканевая ин- женерия 2010;5(1): 33-40.</mixed-citation></ref><ref id="B18"><label>18.</label><mixed-citation>Панин Л.Е., Соколова М.В., Усынин И.Я. Роль мононукле- арной фагоцитирующей системы в регуляции биосинтеза белка в переживающих срезах печени и гепатоцитах белых крыс. Бюлл. экс- пер. биол. мед. 1991; 1: 108-9.</mixed-citation></ref><ref id="B19"><label>19.</label><mixed-citation>Косых А.А., Бесараб И.Ю., Рощина Н.М. Роль соединитель- ной ткани в репаративной регенерации нормальной и цирротически измененной печени. В кн.: Солопаев Б.П. Регенерация, адаптация, гомеостаз. Горький. 1990; 21-30.</mixed-citation></ref><ref id="B20"><label>20.</label><mixed-citation>Michalopoulos G.K, De Frances M.C. Liver regeneration. Science 1997; 276(5309): 60-6</mixed-citation></ref><ref id="B21"><label>21.</label><mixed-citation>Плющ И.В., Цырендоржиев Д.Д., Зубахин А.А. и др. Фило- генная и гемопоэзстимулирующая активности макрофагов печени и легких при регенерации печени. Бюлл. экспер. биол. мед. 1996; 11: 494-8.</mixed-citation></ref><ref id="B22"><label>22.</label><mixed-citation>Masumoto A., Yamamoto N. Cell characterization of a hepatocyte growth factor derived from nonparenchymal liver cells. Struct. Funct. 1993; 18(2): 87-94.</mixed-citation></ref><ref id="B23"><label>23.</label><mixed-citation>Gaca M.D., Pickering J.A., Arthur M.J. et al. Human and rat hepatic stellate cells produce stem cell factor: a possible mechanism for mast cell recruitment in liver fibrosis. J. Hepatol. 1999; 30(5): 850-8.</mixed-citation></ref><ref id="B24"><label>24.</label><mixed-citation>Tsukamoto H. Redox regulation of cytokine expression in Kupffer cells. Antioxid Redox Signal 2002; 4: 741-8.</mixed-citation></ref><ref id="B25"><label>25.</label><mixed-citation>Han Y.P., Zhou L., Wang J. et al. Essential role of matrix metalloproteinases in interleukin-1-induced myofibroblastic activation of hepatic stellate cell in collagen. J. Biol. Chem. 2004; 279: 4820-8.</mixed-citation></ref><ref id="B26"><label>26.</label><mixed-citation>Friedman S., Rockey D. Montgomery B. Hepatic fibrosis 2006: report of the third AASLD single topic conference. Hepatology 2006; 45: 242-9.</mixed-citation></ref><ref id="B27"><label>27.</label><mixed-citation>Schirmacher P., Geerts A., Pietrangelo A. et al. Hepatocyte growth factor/hepatopoietin a is expressed in fat-storing cells from rat liver but not myofibroblast-like cells derived from fat-storing cells. Hepatology 1992; 15: 5-11.</mixed-citation></ref><ref id="B28"><label>28.</label><mixed-citation>Maher J.J. Cell-specific expression of hepatocyte growth factor in liver. upregulation in sinusoidal endothelial cells after carbon tetrachloride. J. Clin. Invest. 1993; 91: 2244-52.</mixed-citation></ref><ref id="B29"><label>29.</label><mixed-citation>Fujio K., Evarts R.P., Hu Z. et al. Expression of stem cell factor and its receptor, c-kit, during liver regeneration from putative stem cells in adult rat. Lab. Invest. 1994; 70: 511-6.</mixed-citation></ref><ref id="B30"><label>30.</label><mixed-citation>Yoshino R., Miura K., Segawa D. et al. Epimorphin expression and stellate cell status in mouse liver injury. Hepatol. Res. 2006, 34: 238-49.</mixed-citation></ref><ref id="B31"><label>31.</label><mixed-citation>Asahina K., Sato H., Yamasaki C. et al. Pleiotrophin/heparinbinding growth-assosiated molecule as a mitogen of rat hepatocytes and its role in regeneration and development of liver. Am. J. Pathol. 2002; 160: 2191-205.</mixed-citation></ref><ref id="B32"><label>32.</label><mixed-citation>Sawitza I., Kordes C., Hausinger D. The niche of stellate cells within rat liver. J. Hepatol. 2009; 50(5): 1617-24.</mixed-citation></ref><ref id="B33"><label>33.</label><mixed-citation>Arenson D.M., Friedman S., Bissel M. Formation of extracellular matrix in normal rat liver: lipocytes as a mayor source of proteoglycan. Gastroenterology 1998; 95: 441-7.</mixed-citation></ref><ref id="B34"><label>34.</label><mixed-citation>Arthur M.J., Friedman S.L., Roll F.J. et al. Lipocytes from normal rat liver release a neutral metalloproteinase that degrades basement membrane (type IV) collagen. J. Clin. Invest. 1989; 84(4): 1076-85.</mixed-citation></ref><ref id="B35"><label>35.</label><mixed-citation>Arthur M.J. Degradation of matrix proteins in liver fibrosis. Pathol. Res. Pract. 1994; 190(9-10): 825-33.</mixed-citation></ref><ref id="B36"><label>36.</label><mixed-citation>Ben S., Li X., Xu F. et al. Treatment with anti-CC chemokine receptor 3 monoclonal antibody or dexamethasone inhibits the migration and differentiation of bone marrow CD34 progenitor cells in an allergic mouse model. Allergy 2008; 63(9): 1164-76.</mixed-citation></ref><ref id="B37"><label>37.</label><mixed-citation>Чалисова Н.И., Князькин И.В., Кветной И.М. Нейроиммуно- эндокринные механизмы действия пептидов и аминокислот в ткане- вых культурах. СПб: Деан; 2005.</mixed-citation></ref><ref id="B38"><label>38.</label><mixed-citation>Ярыгин К.Н. Роль резидентных и циркулирующих стволовых клеток в физиологической и репаративной регенерации печени. Па- тол. Физиол. Экспер. Терапия. 2008; 1: 2-7.</mixed-citation></ref><ref id="B39"><label>39.</label><mixed-citation>Fausto N. Hepatocyte differentiation and liver progenitor cells. Curr. Opin. Cell Biol.1990; 2: 1036-42.</mixed-citation></ref><ref id="B40"><label>40.</label><mixed-citation>Sell S. Is there a liver stem cell? Cancer Res. 1990; 50(13): 3811-5.</mixed-citation></ref><ref id="B41"><label>41.</label><mixed-citation>Sigal S.H., Brill S., Fiorino A.S. et al. The liver as a stem cell and lineage system. Am. J. Physiol. 1992; 263(2 Pt 1): 139-48.</mixed-citation></ref><ref id="B42"><label>42.</label><mixed-citation>Grompe M. The role of bone marrow stem cells in liver regeneration. Semin. Liver Dis. 2003; 23(4): 363-72.</mixed-citation></ref><ref id="B43"><label>43.</label><mixed-citation>Petersen B.E., Grossbard B., Hatch H. et al. Mouse A-6- positive hepatic oval cells also express several hematopoietic stem cell markers. Hepatology 2003; 37: 632-40.</mixed-citation></ref><ref id="B44"><label>44.</label><mixed-citation>Schwartz R.E., Reyes M., Koodie J. et al. Multipotent adult progenitor cells from bone marrow differentiate into functional hepatocyte-like cells. J. Clin. Ivest. 2002: 109: 1291-302.</mixed-citation></ref><ref id="B45"><label>45.</label><mixed-citation>Черных Е.Р., Останин А.А., Пальцев А.И. Стволовые клетки в регенерации печени: новые подходы к лечению печеночной недо- статочности. Гепатология 2004; 5: 24-33.</mixed-citation></ref><ref id="B46"><label>46.</label><mixed-citation>Terada N., Hamazaki T., Oka M. et al. Bone marrow cells adopt the phenotype of other cells by spontaneous cell fusion. Nature 2002;416: 542-5.</mixed-citation></ref><ref id="B47"><label>47.</label><mixed-citation>Гумерова А.А., Киясов А.П., Калигин М.С. и др. Участие клеток Ито в гистогенезе и регенерации печени. Клеточная транс- плантология и тканевая инженерия 2007; 2(4): 39-46.</mixed-citation></ref><ref id="B48"><label>48.</label><mixed-citation>Kiassov A.P., Van Euken P., Van Pelt J.F. et al. Desmin expressing nonhematopoietic liver cells during rat liver development: an immunohistochemical and morphometric study. Differentiation 1995; 59: 253-8.</mixed-citation></ref><ref id="B49"><label>49.</label><mixed-citation>Paku S., Schur J., Nagy P. et al. Origin and structural evolution of the early proliferating oval cells in rat liver. Am. J. Hepatol. 2001; 158: 1313-23.</mixed-citation></ref><ref id="B50"><label>50.</label><mixed-citation>Киясов А.П., Гумерова А.А., Титова М.А. Овальные клетки - предполагаемые стволовые клетки печени или гепатобласты? Клету- точная трансплантология и тканевая инженерия 2006; 2(4): 55-8.</mixed-citation></ref><ref id="B51"><label>51.</label><mixed-citation>Suskind D.L., Muench M.O. Searching for common stem cells of the hepatic and hematopoietic systems in the human fetal liver: CD34+ cytokeratin 7/8+ cells express markers for stellate cells. J. Hepatol. 2004; 40: 261-8.</mixed-citation></ref><ref id="B52"><label>52.</label><mixed-citation>Kordes C., Sawitzal J., Miller-Marbach A. et al. CD34 hepatic stellate cells are progenitor cells. Biochem., Biophys. Res. Commun. 2007, 352(2): 410-7.</mixed-citation></ref><ref id="B53"><label>53.</label><mixed-citation>Yang L., Jung Y., Omenetti A. et al. Fate-mapping evidence that hepatic stellate cells are epithelial progenitors in adult mouse livers. Stem Cells 2008; 26(8): 2104-13.</mixed-citation></ref><ref id="B54"><label>54.</label><mixed-citation>Wang P., Liu T., Cong M. et al. Expression of extracellular matrix genes in cultured hepatic oval cells: an origin of hepatic stellate cells through transforming growth factor beta? Liver Int. 2009; 29(4): 575-84.</mixed-citation></ref><ref id="B55"><label>55.</label><mixed-citation>Han Y.P., Yan C., Zhou L. et al. A matrix metalloproteinase-9 activation cascade by hepatic stellate cells in trans-differentiation in the three-dimensional extracellular matrix. J. Biol. Chem. 2007; 282(17): 12928-39.</mixed-citation></ref><ref id="B56"><label>56.</label><mixed-citation>Arthur M.J., Stanley A., Iredale J.P. et al. Secretion of 72 kDa type IV collagenase/gelatinase by cultured human lipocytes. Analysis of gene expression, protein synthesis and proteinase activity. J. Biochem. 1992; 287 (3): 701-7.</mixed-citation></ref><ref id="B57"><label>57.</label><mixed-citation>Schaefer B., Rivas-Estilla A.M., Meraz-Cruz N. et al. Reciprocal modulation of matrix metalloproteinase-13 and type I collagen genes in rat hepatic stellate cells. Am. J. Pathol. 2003; 162(6): 1771-80.</mixed-citation></ref><ref id="B58"><label>58.</label><mixed-citation>Petersen B.E., Bowen W.C., Patrene K.D. et al. Bone marrow as a potential source of hepatic oval cells. Science 1999; 284(5417): 1168-70.</mixed-citation></ref><ref id="B59"><label>59.</label><mixed-citation>Sato Y., Araki H., Kato J. et al. Human mesenchymal stem cells xenografted directly to rat liver are differentiated into human hepatocytes without fusion. Blood 2005; 106(2): 756-63.</mixed-citation></ref><ref id="B60"><label>60.</label><mixed-citation>Taléns-Visconti R., Bonora A., Jover R. et al. Hepatogenic differentiation of human mesenchymal stem cells from adipose tissue in comparison with bone marrow mesenchymal stem cells. World J. Gastroenterol. 2006; 12(36): 5834-45.</mixed-citation></ref><ref id="B61"><label>61.</label><mixed-citation>Taléns-Visconti R., Bonora A., Jover R. et al. Human mesenchymal stem cells from adipose tissue: Differentiation into hepatic lineage. Toxicol. In Vitro. 2007; 21(2): 324-9.</mixed-citation></ref><ref id="B62"><label>62.</label><mixed-citation>Lange C., Bruns H., Kluth D. et al. Hepatocytic differentiation of mesenchymal stem cells in cocultures with fetal liver cells. World J. Gastroenterol. 2006; 12(15): 2394-7.</mixed-citation></ref><ref id="B63"><label>63.</label><mixed-citation>Киясов A.П., Исламов Р.Р., Ризванов А.А. и др. Клеточная терапия генетически модифицированными стволовыми клетками пуповинной крови трансгенных G93A мышей, экспрессирующих фенотип бокового амиотрофического склероза. Итоговая конфе- ренция по результатам выполнения мероприятий за 2007 год в рамках приоритетного направления «Живые системы» ФЦП «Ис- следования и разработки по приоритетным направлениям развития научно-технологического комплекса России на 2007-2012 годы». Москва: 2007; 65-6.</mixed-citation></ref><ref id="B64"><label>64.</label><mixed-citation>Baba S., Fujii H., Hirose T. et al. Commitment of bone marrow cells to hepatic stellate cells in mouse. J. Hepatol. 2004; 40: 255-60.</mixed-citation></ref><ref id="B65"><label>65.</label><mixed-citation>Hoppo T., Fujii H., Hirose T. et al. Thy1-positive mesenchymal cells promote the maturation of CD49f-positive hepatic progenitor cells in the mouse fetal liver. Hepatology 2004; 39(5): 1362-70.</mixed-citation></ref><ref id="B66"><label>66.</label><mixed-citation>Dezso K., Jelnes P., László V. et al. Thy-1 is expressed in hepatic myofibroblasts and not oval cells in stem cell-mediated liver regeneration. Am. J. Pathol. 2007; 171(5): 1529-37.</mixed-citation></ref><ref id="B67"><label>67.</label><mixed-citation>Tocci A., Parolini I., Gabbianelli M. et al. Dual action of retinoic acid on human embryonic/fetal hematopoiesis: blockade of primitive progenitor proliferation and shift from multipotent/erythroid/monocytic to granulocytic differentiation program. Blood 1996; 88(8): 2878-88.</mixed-citation></ref><ref id="B68"><label>68.</label><mixed-citation>Watt F.M., Hogan B.L. Out of Eden: stem cells and their niches. Science 2000; 287(5457): 1427-30.</mixed-citation></ref><ref id="B69"><label>69.</label><mixed-citation>Колпащикова И.Ф. Общие и местные изменения в организ- ме при экспериментальном повреждении печени и ее регенерации (диссертация). Казань 1982.</mixed-citation></ref><ref id="B70"><label>70.</label><mixed-citation>Marra F., Efsen E., Romanelli R.G. et al. Ligands of peroxisome proliferator-activated receptor gamma modulate profibrogenic and proinflammatory actions in hepatic stellate cells. Gastroenterology 2000; 119: 466-78.</mixed-citation></ref><ref id="B71"><label>71.</label><mixed-citation>Canbay A., Taimr P., Torok N. et al. Apoptotic body engulfment by a human stellate cell line is profibrogenic. Lab. Invest. 2003; 83: 655-63.</mixed-citation></ref><ref id="B72"><label>72.</label><mixed-citation>Safadi R., Ohta M., Alvarez C.E. et al. Immune stimulation of hepatic fibrogenesis by CD8 cells and attenuation by transgenic interleukin-10 from hepatocytes. Gastroenterology 2004; 127(3): 870-82.</mixed-citation></ref><ref id="B73"><label>73.</label><mixed-citation>Viñas O., Bataller R., Sancho-Bru P. et al. Human hepatic stellate cells show features of antigen-presenting cells and stimulate lymphocyte proliferation. Hepatology 2003; 38: 919-29.</mixed-citation></ref><ref id="B74"><label>74.</label><mixed-citation>Wynn, T.A. Cellular and molecular mechanisms of fibrosis. J. Pathol. 2008; 214: 199-210.</mixed-citation></ref><ref id="B75"><label>75.</label><mixed-citation>Dai L.J, Li H.Y. The therapeutic potential of bone marrowderived mesenchymal stem cells on hepatic cirrhosis. Stem Cell Res. 2009; 2(1): 16-25.</mixed-citation></ref><ref id="B76"><label>76.</label><mixed-citation>Pinzani M. PDGF and signal transduction in hepatic stellate cells. Front. Biosci. 2002; 7: 1720-6.</mixed-citation></ref><ref id="B77"><label>77.</label><mixed-citation>Gressner A.M., Weiskirchen R., Breitkopf K. et al. Roles of TGF-beta in hepatic fibrosis. Front. Biosci. 2002; 17: 793-807.</mixed-citation></ref><ref id="B78"><label>78.</label><mixed-citation>Wells R.G., Kruglov E., Dranoff J.A. Autocrine release of TGFbeta by portal fibroblasts regulates cell growth. FEBS Lett. 2004; 559(1-3): 107-10.</mixed-citation></ref><ref id="B79"><label>79.</label><mixed-citation>Arthur M.J. Reversibility of liver fibrosis and cirrhosis following treatment for hepatitis C. Gastroenterology 2002; 122: 1525-8.</mixed-citation></ref><ref id="B80"><label>80.</label><mixed-citation>Issa R., Zhou X., Constandinou C.M. et al. Spontaneous recovery from micronodular cirrhosis: evidence for incomplete resolution associated with matrix cross-linking. Gastroenterology 2004; 126: 1795-808.</mixed-citation></ref><ref id="B81"><label>81.</label><mixed-citation>Friedman S.L. Reversibility of hepatic fibrosis and cirrhosis - is it all hype? Nat. Clin. Pract. Gastroenterol. Hepatol. 2007; 4: 236-7.</mixed-citation></ref><ref id="B82"><label>82.</label><mixed-citation>Parekkadan B., Poll D., Suganuma K. et al.. Mesenchymal stem cell-derived molecules reverse fulmimant hepatic failure. PLoS One 2007; 2(9): e941.</mixed-citation></ref><ref id="B83"><label>83.</label><mixed-citation>Parekkadan B., Poll D., Megeed Z. et al.. Immunomodulation of hepatic stellate cells by mesenchymal stem cells. Biochem. Biophys. Res. Commu. 2007, 363; 247-52.</mixed-citation></ref><ref id="B84"><label>84.</label><mixed-citation>Poll D., Parekkadan B., Cho C.H. et al. Mesenchymal stem cellderived molecules directly modulate hepatocellular death and regeneration in vitro and in vivo. Hepatology 2008; 47: 1634-43.</mixed-citation></ref><ref id="B85"><label>85.</label><mixed-citation>Sakaida I. et al. Cell therapy with bone marrow cell for liver cirrhosis. Electrophoresis 2006; 50: 7-12.</mixed-citation></ref><ref id="B86"><label>86.</label><mixed-citation>Sakaida I., Terai S., Yamamoto N. et al. Transplantation of bone marrow cells reduces CCl4-induced liver fibrosis in mice. Hepatology 2004; 40: 1304-11.</mixed-citation></ref><ref id="B87"><label>87.</label><mixed-citation>Terai S., Sakaida I., Yamamoto N. et al. An in vivo model for monitoring transdifferentiation of bone marrow cells into functional hepatocytes. J. Biochem. 2003; 134: 551-8.</mixed-citation></ref><ref id="B88"><label>88.</label><mixed-citation>Terai S., Ishikawa T., Omori K. et al. Improved liver function in patients with liver cirrhosis after autologous bone marrow cell infusion therapy. Stem Cells 2006; 24(10): 2292-8.</mixed-citation></ref><ref id="B89"><label>89.</label><mixed-citation>Kuo T.K., Hung S. et al. Stem cell therapy for liver disease: parameters governing the success for using bone marrow mesenchymal stem cells. Gastroenterology 2008; 134: 2111-21.</mixed-citation></ref><ref id="B90"><label>90.</label><mixed-citation>Yu Y., Yao A.H., Chen N., et al. Mesenchymal stem cells overexpressing hepatocyte growth factor improve small-for-size liver grafts regeneration. Mol. Ther. 2007; 15:1382-9.</mixed-citation></ref><ref id="B91"><label>91.</label><mixed-citation>Yagi K., Kojima M., Oyagi S. et al. Application of mesenchymal stem cells to liver regenerative medicine. Yakugaku Zasshi. 2008; 128: 3-9.</mixed-citation></ref><ref id="B92"><label>92.</label><mixed-citation>Киясов А.П.,. Одинцова А.Х, Гумерова А.А. и др. Транс- плантация аутогенных гемопоэтических стволовых клеток больным хроническими гепатитами. Клеточная трансплантология и тканевая инженерия 2008; 3(1): 70-5.</mixed-citation></ref><ref id="B93"><label>93.</label><mixed-citation>Pulavendran S., Vignesh J., Rose C. Differential antiinflammatory and anti-fibrotic activity of transplanted mesenchymal vs. hematopoietic stem cells in carbon tetrachloride-induced liver injury in mice. Int. Immunopharmacol. 2010; 10(4): 513-9.</mixed-citation></ref><ref id="B94"><label>94.</label><mixed-citation>Theise N.D., Nimmakayalu M., Gardner R. et al. Liver from bone marrow in humans. Hepatology 2000; 32: 11-6.</mixed-citation></ref><ref id="B95"><label>95.</label><mixed-citation>Alison M.R., Poulsom R., Jeffery R. et al. Hepatocytes from non-hepatic adult stem cells. Nature 2000; 406: 257.</mixed-citation></ref><ref id="B96"><label>96.</label><mixed-citation>Kakinuma S., Tanaka Y., Chinzei R. et al. Human umbilical stem cell cord blood as a source of transplantable hepatic progenitor cells. Stem cells 2003; 21: 217-27.</mixed-citation></ref><ref id="B97"><label>97.</label><mixed-citation>Wang X., Willenbring H., Akkary Y. et al. Cell fusion is the principal source of bone marrow-derived hepatocytes. Nature 2003; 422: 897-901.</mixed-citation></ref><ref id="B98"><label>98.</label><mixed-citation>Korbling M., Katz R.L., Khanna A. et al. Hepatocytes and epithelial cells of donor origin in recipients of peripheral blood stem cells. N. Engl. J. Med. 2002; 346(10): 738-46.</mixed-citation></ref><ref id="B99"><label>99.</label><mixed-citation>Zhang Z.X., Guan L.X., Zhang K. et al. A combined procedure to deliver autologous mesenchymal stromal cells to patients with traumatic brain injury. Cytotherapy 2008; 10: 134-9.</mixed-citation></ref><ref id="B100"><label>100.</label><mixed-citation>Xiang G.A., Zhang G.Q., Fang C.H. et al. A preliminary study of the homing capacity of allograft mesenchymal stem cells to rat liver. Di Yi Junyi Daxue Xuebao 2005; 25: 994-7.</mixed-citation></ref><ref id="B101"><label>101.</label><mixed-citation>Petersen B.E. Hepatic stem cells: coming full circle. Blood cells mol. Dis. 2001; 27(3): 590-600.</mixed-citation></ref><ref id="B102"><label>102.</label><mixed-citation>Fox J.M., Chamberlain G., Ashton B.A. et al. Recent advances into the understanding of mesenchymal stem cell trafficking. Br. J. Haematol. 2007; 137: 491-502.</mixed-citation></ref><ref id="B103"><label>103.</label><mixed-citation>Dalakas E., Newsome P.N., Harrison D.J. et al. Hematopoietic stem cell trafficking in liver injury. FASEB 2005; 19(10): 1225-31.</mixed-citation></ref><ref id="B104"><label>104.</label><mixed-citation>Avital J., Inderbitzin D., Aoki T. et al. Isolation, characterization and transplantation of bone marrow-derived hepatocyte stem cells. Bioch., Biophys. Res. Communic. 2001; 288: 156-64.</mixed-citation></ref><ref id="B105"><label>105.</label><mixed-citation>Fiegel H.C., Lioznov M.V. et al. Liver-specific gene expression in cultured human hematopoietic stem cells. Stem cells 2003; 21(1): 98-104.</mixed-citation></ref><ref id="B106"><label>106.</label><mixed-citation>Zhao Y., Glesne D., Huberman E. A human peripheral blood monocyte-derived subset acts as pluripotent stem cells. PNAS USA 2003; 100: 2426-31.</mixed-citation></ref><ref id="B107"><label>107.</label><mixed-citation>Jiang Y., Jahagirdar B.N., Reinhardt R.L. et al. Pluripotency of mesenchimal stem cells derived from adult marrow. Nature 2002; 418: 41-9.</mixed-citation></ref><ref id="B108"><label>108.</label><mixed-citation>Lee K.D., Kuo T.K., Whang-Peng Y et al. In vitro hepatic differentiation of human mesenchymal stem cells. Hepatology 2004; 40: 1256-9.</mixed-citation></ref><ref id="B109"><label>109.</label><mixed-citation>Lange C., Bassler P., Lioznov M.V. Liver-specific gene expression in mesenchymal stem cells is induced by liver cells. World J. Gastroenterol. 2005; 11: 4497-504.</mixed-citation></ref><ref id="B110"><label>110.</label><mixed-citation>Ong S.Y., Dai H., Leong K.W. Inducing hepatic differentiation of human mesenchymal stem cells in pellet culture. Biomaterials 2006; 27: 4087-97.</mixed-citation></ref><ref id="B111"><label>111.</label><mixed-citation>Lagasse E., Connors H., Al-Dhalimy M. et al. Purified hematopoietic stem cells can differentiate into hepatocytes in vivo. Nat. Med. 2000; 6: 1229-34.</mixed-citation></ref><ref id="B112"><label>112.</label><mixed-citation>Miyazaki M., Akiyama I., Sacaguchi M. et al. Improved conditions to induce hepatocytes from rat bone marrow cells in culture. Biochem. Biophys. Res. Commun. 2002; 298: 24-30.</mixed-citation></ref><ref id="B113"><label>113.</label><mixed-citation>Fontanellas A., Mazurier F., Landry M. et al. Reversion of hepatobilary alterations by bone marrow transplantation in a murine model of erythropoietic protoporphyria. Hepatology 2000; 32: 73-81.</mixed-citation></ref><ref id="B114"><label>114.</label><mixed-citation>Chamberlain J., Yamagami T., Colletti E. et al. Efficient generation of human hepatocytes by the intrahepatic delivery of clonal human mesenchymal stem cells in fetal sheep. Hepatology 2007; 46: 1935-45.</mixed-citation></ref><ref id="B115"><label>115.</label><mixed-citation>Camargo F.D., Finegold M., Goodell M.A. Hematopoietic myelomonocytic cells are the major source of hepatocyte fusion partners. J. Clin. Invest. 2004; 113: 1266-70.</mixed-citation></ref><ref id="B116"><label>116.</label><mixed-citation>Willenbring H., Bailey A.S., Foster M. et al., Myelomonocytic cells are sufficient for therapeutic cell fusion in liver. Nat. Med. 2004; 10: 774-48.</mixed-citation></ref><ref id="B117"><label>117.</label><mixed-citation>Russo F.P., Alison M.R., Bigger B.W. et al. The bone marrow functionally contributes to liver fibrosis. Gastroenterology 2006; 130: 1807-21.</mixed-citation></ref><ref id="B118"><label>118.</label><mixed-citation>Fausto N., Webber E.M. Liver regeneration. 2 Role of growth factors and cytokines in hepatic regeneration. FASEB 1995; 9: 1527-36.</mixed-citation></ref><ref id="B119"><label>119.</label><mixed-citation>Galun E., Axelrod J.H. The role of cytokines in liver failure and regeneration: potential new molecular therapies. Biochym. Biophys Acta. 2002; 1592: 345-58.</mixed-citation></ref><ref id="B120"><label>120.</label><mixed-citation>Kinnard T., Stabile E., Burnett M.S. et al. Marrow-derived stromal cells express genes encoding a broad spectrum of arterigenic cytokines and promote in vitro and in vivo arteriogenesis though paracrine mechanisms. Circul. Res., 2004; 94: 678-82.</mixed-citation></ref><ref id="B121"><label>121.</label><mixed-citation>Liu C.H., Hwang S.M. Cytokine interactions in mesenchymal stem cells from cord blood. Cytokine 2005; 32: 270-9.</mixed-citation></ref><ref id="B122"><label>122.</label><mixed-citation>Linker R.A., Kruse N., Israel S. et al. Leukemia inhibitory factor deficiency modulates the immune response and limits autoimmune demyelination: a new role for neutrophic cytokines in neuroinflammation. J. Immunol. 2008; 180: 2204-13.</mixed-citation></ref><ref id="B123"><label>123.</label><mixed-citation>Chen X., Li Y., Wang L. et al.. Ischemic rat brain extracts induce human marrow stromal cell growth factor production. Neuropathol. 2002; 22: 275-9.</mixed-citation></ref><ref id="B124"><label>124.</label><mixed-citation>Ren X., Colletti L. et al. Stem cell factor restores hepatocyte proliferation in IL-6 knockout mice following 70% hepatectomy. J. Clin. Invest. 2003; 112: 1407-18.</mixed-citation></ref><ref id="B125"><label>125.</label><mixed-citation>Langer D.A., Das A., Semela D. et al. Nitricoxide promotes caspase-independent hepatic stellate cell apoptosis through the generation of reactive oxygen species. Hepatology 2008; 47: 1983-93</mixed-citation></ref><ref id="B126"><label>126.</label><mixed-citation>Marubashi S., Sakon M., Nagano H. et al. Effect of portal hemodynamics on liver regeneration studied in a novel portohepatic shunt rat model. Surgery 2004; 136: 1028-37.</mixed-citation></ref><ref id="B127"><label>127.</label><mixed-citation>Fausto N., Riehle K.J. Mechanisms of liver regeneration and their clinical implications. J. Hepatobiliary Pancreat. Surg. 2005; 12: 181-9.</mixed-citation></ref><ref id="B128"><label>128.</label><mixed-citation>Ren G., Zhang L., Zhao X. et al.. Mesenchymal stem cell-mediated immunosuppression occurs via concerted action of chemokines and nitric oxide. Cell Stem Cell 2008; 2: 141-50.</mixed-citation></ref><ref id="B129"><label>129.</label><mixed-citation>Mohamadnejad M., Namiri M., Bagheri M. et al. Phase 1 human trial of autologous bone marrow-hematopoietic stem cell transplantation in patients with decompensated cirrhosis. World J.Gastroenterol. 2007; 13: 3359-63.</mixed-citation></ref><ref id="B130"><label>130.</label><mixed-citation>Yagi H., Soto-Gutierrez A., Navarro-Alvarez N. et al. Reactive bone marrow stromal cells attenuate systemic inflammation via sTNFR1. Mol. Ther. 2010; 18(10): 1857-64.</mixed-citation></ref><ref id="B131"><label>131.</label><mixed-citation>Honczarenko M., Le Y., Swierkowski M. et al. Human bone marrow stromal cells express a distinct set of biologically functional chemokine receptors. Stem Cells, 2006, 24, 1030-1041.</mixed-citation></ref><ref id="B132"><label>132.</label><mixed-citation>Lee M.J., Jung J., Na K.H. et al. Anti-fibrotic effect of chorionic plate-derived mesenchymal stem cells isolated from human placenta in a rat model of CCl(4)-injured liver: potential application to the treatment of hepatic diseases. J. Cell Biochem. 2010; 111(6): 1453-63.</mixed-citation></ref><ref id="B133"><label>133.</label><mixed-citation>Gasbarrini A., Rapaccini G.L., Rutella S et al. Rescue therapy by portal infusion of autologous stem cells in a case of drug-induced hepatitis. Dig. Liver Dis. 2007; 39: 878-82.</mixed-citation></ref><ref id="B134"><label>134.</label><mixed-citation>Knoefel W.T., Klein M. et al. Portal application of autologous CD133+ bone marrow cells to the liver: a novel concept to support hepatic regeneration. Stem Cells 2005; 23: 463-70.</mixed-citation></ref><ref id="B135"><label>135.</label><mixed-citation>Kallis Y.N., Alison M.R., Forbes S.J. Bone marrow stem cells and liver disease. Gut 2007; 56: 716-24.</mixed-citation></ref><ref id="B136"><label>136.</label><mixed-citation>Mohamadnejad M., Alimoghaddam K., Mohyeddin-Bonab M. et al. Phase 1 trial of autologous bone marrow mesenchymal stem cell transplantation in patients with decompensated liver cirrhosis. Arch. Iran Med. 2007; 10: 459-66.</mixed-citation></ref><ref id="B137"><label>137.</label><mixed-citation>Carvalho A.B., Quintannilha L.F., Dias et al. Bone marrow multipotent mesenchymal stem cells do not reduce fibrosis or improve function in a rat model of severe chronic liver injury. Stem Cells 2008; 26: 1307-14.</mixed-citation></ref><ref id="B138"><label>138.</label><mixed-citation>Peng L., Li H., Gu L. et al. Comparison of biological characteristics of marrow mesenchymal stem cells in hepatitis B patients and normal adults. World J. Gastroenterol. 2007; 13:1743-6.</mixed-citation></ref><ref id="B139"><label>139.</label><mixed-citation>Fox I.J., Strom S.C. To be or not to be: generation of hepatocytes from cells outside the liver. Gastroenterology 2008; 134: 878-81.</mixed-citation></ref><ref id="B140"><label>140.</label><mixed-citation>Zhang Z.X., Guan L.X., Zhang K. et al. Cytogenetic analysis of human bone marrow-derived mesenchymal stem cells passaged in vitro. Cell Biol. Int. 2007; 31: 645-8.</mixed-citation></ref><ref id="B141"><label>141.</label><mixed-citation>Dugast A., Vanhove B. Immune regulation by non-lymphoid cells in transplantation. Clin. Exp. Immunol. 2009; 156(1): 25-34.</mixed-citation></ref><ref id="B142"><label>142.</label><mixed-citation>Aziz M.T., Atta H.M., Mahfouz S. et al. Therapeutic potential of bone marrow-derived mesenchymal stem cells on experimental liver fibrosis. Clin. Biochem. 2007; 40: 893-9.</mixed-citation></ref><ref id="B143"><label>143.</label><mixed-citation>Zhao D.C., Lei J.X., Chen R. et al. Bone marrow-derived mesenchymal stem cells protect against experimental liver fibrosis in rat. World J. Gastroentrol. 2005; 14: 3431-40</mixed-citation></ref><ref id="B144"><label>144.</label><mixed-citation>Fang B., Shi M., Liao L. et al. Systemic infusion of FLK1+ mesenchymal stem cells ameliorate carbon tetrachloride-induced liver fibrosis in mice. Transplant. 2004; 78: 83-8.</mixed-citation></ref><ref id="B145"><label>145.</label><mixed-citation>Murphy F.R., Issa R., Zhou X. et al. Inhibition of apoptosis of activated hepatic stellate cells by tissue inhibitor of metalloproteinase-1 is mediated via effects on matrix metalloproteinase inhibition. J. Biol. Chem. 2002; 277: 11069-76.</mixed-citation></ref><ref id="B146"><label>146.</label><mixed-citation>Higashiyama R., Inagaki Y., Hong Y.Y. et al. Bone marrowderived cells express matrix metalloproteinases and contribute to regression of liver fibrosis in mice. Hepatology 2007; 45: 213-22.</mixed-citation></ref><ref id="B147"><label>147.</label><mixed-citation>Bonzo L.V., Ferrero I., Cravanzola C. et al. Human mesenchymal stem cells as a two-edged sword in hepatic regenerative medicine: engraftment and hepatocyte differentiation versus profibrogenic potential. Gut 2008; 57: 223-31.</mixed-citation></ref></ref-list></back></article>
