<?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">121670</article-id><article-id pub-id-type="doi">10.23868/gc121670</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">Tsirkuliruyushchie gemopoeticheskie i endotelial'nyepredshestvenniki v perifericheskoy krovi patsientovs cherepno-mozgovoy travmoy</article-title><trans-title-group xml:lang="ru"><trans-title>Циркулирующие гемопоэтические и эндотелиальныепредшественники в периферической крови пациентовс черепно-мозговой травмой</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Chernykh</surname><given-names>V A</given-names></name><name xml:lang="ru"><surname>Черных</surname><given-names>В А</given-names></name></name-alternatives><bio xml:lang="en"><p>Institute of travmatology and orthopedy, Novosibirsk</p></bio><bio xml:lang="ru"><p>НИИ травматологии и ортопедии Росмедтехнологий, Новосибирск</p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Pronkina</surname><given-names>N V</given-names></name><name xml:lang="ru"><surname>Пронкина</surname><given-names>Н В</given-names></name></name-alternatives><bio xml:lang="en"><p>Institute of clinical immunology SB RAMS, Novosibirsk</p></bio><bio xml:lang="ru"><p>Институт клинической иммунологии СО РАМН, Новосибирск</p></bio><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Stupak</surname><given-names>V V</given-names></name><name xml:lang="ru"><surname>Ступак</surname><given-names>В В</given-names></name></name-alternatives><bio xml:lang="en"><p>Institute of travmatology and orthopedy, Novosibirsk</p></bio><bio xml:lang="ru"><p>НИИ травматологии и ортопедии Росмедтехнологий, Новосибирск</p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Fonin</surname><given-names>V V</given-names></name><name xml:lang="ru"><surname>Фонин</surname><given-names>В В</given-names></name></name-alternatives><bio xml:lang="en"><p>City clinical hospital №1, Novosibirsk</p></bio><bio xml:lang="ru"><p>Городская клиническая больница №1, Новосибирск</p></bio><xref ref-type="aff" rid="aff3"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Shishlov</surname><given-names>P E</given-names></name><name xml:lang="ru"><surname>Шишлов</surname><given-names>П Е</given-names></name></name-alternatives><bio xml:lang="en"><p>City clinical hospital №1, Novosibirsk</p></bio><bio xml:lang="ru"><p>Городская клиническая больница №1, Новосибирск</p></bio><xref ref-type="aff" rid="aff3"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Shevela</surname><given-names>E Ya</given-names></name><name xml:lang="ru"><surname>Шевела</surname><given-names>Е Я</given-names></name></name-alternatives><bio xml:lang="ru"><p>Институт клинической иммунологии СО РАМН, Новосибирск</p></bio><xref ref-type="aff" rid="aff4"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Leplina</surname><given-names>O Yu</given-names></name><name xml:lang="ru"><surname>Леплина</surname><given-names>О Ю</given-names></name></name-alternatives><bio xml:lang="en"><p>Institute of clinical immunology SB RAMS, Novosibirsk</p></bio><bio xml:lang="ru"><p>Институт клинической иммунологии СО РАМН, Новосибирск</p></bio><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Chernykh</surname><given-names>E R</given-names></name><name xml:lang="ru"><surname>Черных</surname><given-names>Е Р</given-names></name></name-alternatives><bio xml:lang="en"><p>Institute of clinical immunology SB RAMS, Novosibirsk</p></bio><bio xml:lang="ru"><p>Институт клинической иммунологии СО РАМН, Новосибирск</p></bio><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Ostanin</surname><given-names>A A</given-names></name><name xml:lang="ru"><surname>Останин</surname><given-names>А А</given-names></name></name-alternatives><bio xml:lang="en"><p>Institute of clinical immunology SB RAMS, Novosibirsk</p></bio><bio xml:lang="ru"><p>Институт клинической иммунологии СО РАМН, Новосибирск</p></bio><xref ref-type="aff" rid="aff2"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Institute of travmatology and orthopedy, Novosibirsk</institution></aff><aff><institution xml:lang="ru">НИИ травматологии и ортопедии Росмедтехнологий, Новосибирск</institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">Institute of clinical immunology SB RAMS, Novosibirsk</institution></aff><aff><institution xml:lang="ru">Институт клинической иммунологии СО РАМН, Новосибирск</institution></aff></aff-alternatives><aff-alternatives id="aff3"><aff><institution xml:lang="en">City clinical hospital №1, Novosibirsk</institution></aff><aff><institution xml:lang="ru">Городская клиническая больница №1, Новосибирск</institution></aff></aff-alternatives><aff-alternatives id="aff4"><aff><institution xml:lang="en"></institution></aff><aff><institution xml:lang="ru">Институт клинической иммунологии СО РАМН, Новосибирск</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>71</fpage><lpage>77</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/121670">https://genescells.ru/2313-1829/article/view/121670</self-uri><abstract xml:lang="ru"><p>В настоящей работе исследована мобилизация ге-
мопоэтических стволовых/прогениторных клеток (ГСК)
и эндотелиальных предшественников (ЭП) у больных с
черепно-мозговой травмой (ЧМТ). В первые 24-48 ч по-
сле ЧМТ выявлено достоверное возрастание абсолютного
количества циркулирующих CD34+CD45+ГСК, а также от-
носительного и абсолютного количества CD34+CD144+ЭП.
Эффективность мобилизации ГСК была достоверно выше
в группе больных до 40 лет, и относительное содержание
CD45+CD34+ клеток находилось в обратной зависимости
от возраста пациентов (r = -0,54, р = 0,039). Возрас-
тание CD45+CD34+ГСК и CD34+CD144+ЭП регистриро-
валось как у больных с легкой, так и среднетяжелой/тя-
желой ЧМТ и не зависело от уровня сознания по шкале
комы Глазго (ШКГ). Однако у больных с отсутствием воз-
растания CD45+CD34+ клеток частота неблагоприятных
исходов (1-3 балла по шкале исходов Глазго; ШИГ) была
достоверно выше, чем в подгруппе больных с повышенным
количеством ГСК (p = 0,047). Выявлена также значимая
взаимосвязь ранних ЭП, не экспрессирующих VE-кадгерин
(CD3-CD34+CD144-ЭП), с тяжестью/исходом ЧМТ (r = 0,6;
p = 0,017 и r = 0,53; p = 0,035, соответственно). Таким
образом, интенсивность мобилизации ГСК и ЭП у больных
ЧМТ может быть использована в качестве прогностического
фактора, свидетельствующего о репаративном потенциале
костномозговых предшественников.</p></abstract></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Masuda H., Asahara T. Post-natal endothelial progenitor cells for neovascularization in tissue regeneration. Cardiovasc. Res. 2003; 58: 390-8.</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Schatteman G.C., Dunnwald M., Jiao C. Biology of bone marrowderived endothelial cell precursors. Am. J. Physiol. Heart. Circ. Physiol. 2007; 292: 1-18</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>Asahara T, Masuda H, Takahashi T et al. Bone marrow origin of endothelial progenitor cells responsible for postnatal vasculogenesis in physiological and pathological neovascularization. Circ. Res. 1999; 85: 221-8.</mixed-citation></ref><ref id="B4"><label>4.</label><mixed-citation>Rookmaaker M.B., Verhaar M.C., Loomans C.J. et al. CD34+ cells home, proliferate, and participate in capillary formation, and in combination with CD34-cells enhance tube formation in a 3-dimensional matrix. Arterio. Thromb. Vasc. Biol. 2005; 25; 1-8.</mixed-citation></ref><ref id="B5"><label>5.</label><mixed-citation>Zhang Z.G., Zhang L., Jiang Q. et al Bone marrow-derived endothelial progenitor cells participate in cerebral neovascularization after focal cerebral ischemia in the adult mouse. Circ. Res. 2002; 90: 284-8.</mixed-citation></ref><ref id="B6"><label>6.</label><mixed-citation>Fujita Y., Ihara M., Ushiki T. et al. Early protective effect of bone marrow mononuclear cells against ischemic white matter damage through augmentation of cerebral blood flow. Stroke 2010; 41: 2938-43.</mixed-citation></ref><ref id="B7"><label>7.</label><mixed-citation>Taguchi A., Soma T., Tanaka H. et al. Administration of CD34+ cells after stroke enhances neurogenesis via angiogenesis in a mouse model. J. Clin. Invest. 2004; 114: 330-8.</mixed-citation></ref><ref id="B8"><label>8.</label><mixed-citation>Majka M., Janowska-Wieczorek A., Ratajczak J. et al. Numerous growth factors, cytokines, and chemokines are secreted by human CD34+ cells, myeloblasts, erythroblasts, and megakaryoblasts and regulate normal hematopoiesis in an autocrine/paracrine manner. Blood 2001; 97: 3075-85.</mixed-citation></ref><ref id="B9"><label>9.</label><mixed-citation>Ohab J.J., Fleming S., Blesch A. et al. Neurovascular niche for neurogenesis after stroke. J. Neurosci. 2006; 26: 13007-16.</mixed-citation></ref><ref id="B10"><label>10.</label><mixed-citation>Paczkowska E., Larysz B., Rzeuski R. et al. Human hematopoietic stem/progenitor-enriched CD34+ cells are mobilized into peripheral blood during stress related to ischemic stroke or acute myocardial infarction. Eur. J. Haematol. 2005; 75: 461-7.</mixed-citation></ref><ref id="B11"><label>11.</label><mixed-citation>Shintani S, Murohara T, Ikeda H et al. Mobilization of endothelial progenitor cells in patients with acute myocardial infarction. Circulation 2001; 103: 2776-9.</mixed-citation></ref><ref id="B12"><label>12.</label><mixed-citation>Machalinski B., Paczkowska E., Koziarska D. et al. Mobilization of human hematopoietic stem/progenitor-enriched CD34+ ells into peripheral blood during stress related to ischemic stroke. Folia Histochem. Cytobiol. 2006; 44: 97-101.</mixed-citation></ref><ref id="B13"><label>13.</label><mixed-citation>Sobrino T., Hurtado O., Moro M. A. et al. The increase of circulating endothelial progenitor cells after acute ischemic stroke is associated with good outcome. Stroke 2007; 38: 2759-64.</mixed-citation></ref><ref id="B14"><label>14.</label><mixed-citation>Dunac A., Frelin C., Popolo-Blondeau M. et al. Neurological and functional recovery in human stroke are associated with peripheral blood CD34+ cell mobilization. Neurology 2007; 254: 327-32.</mixed-citation></ref><ref id="B15"><label>15.</label><mixed-citation>Xiong Y., Lu D., Qu C. et al. Effects of erythropoietin on reducing brain damage and improving functional outcome after traumatic brain injury in mice. J. Neurosurg. 2008; 109: 510-21.</mixed-citation></ref><ref id="B16"><label>16.</label><mixed-citation>Richardson R.M., Sun D., Bullock M.R. Neurogenesis after traumatic brain injury. Neurosurg. Clin. N. Am. 2007; 18: 169-81.</mixed-citation></ref><ref id="B17"><label>17.</label><mixed-citation>Morgan R., Kreipke C.W., Roberts G. et al. Neovascularization following traumatic brain injury: possible evidence for both angiogenesis and vasculogenesis. Neurol. Res. 2007; 29: 375-81.</mixed-citation></ref><ref id="B18"><label>18.</label><mixed-citation>Xiong Y., Mahmood A., Chopp M. Angiogenesis, neurogenesis and brain recovery of function following injury. Curr. Opin. Investig. Drugs 2010; 11: 298-308.</mixed-citation></ref><ref id="B19"><label>19.</label><mixed-citation>Liu L., Liu H., Jiao J. et al. Changes in circulating human endothelial progenitor cells after brain injury. Neurotrauma 2007; 24(6): 936-43.</mixed-citation></ref><ref id="B20"><label>20.</label><mixed-citation>Scheubel R.J., Zorn H., Silber R-E. et al. Age-dependent depression in circulating endothelial progenitor cells inpatients undergoing coronary artery bypass grafting. J. Am. Coll. Cardiol. 2003; 42: 2073-80.</mixed-citation></ref><ref id="B21"><label>21.</label><mixed-citation>Redondo S., Hristov M., Gordillo-Moscoso A.A. et al. High-reproducible flow cytometric endothelial progenitor cell determination in human peripheral blood as CD34+/CD144+/CD3- lymphocyte subpopulation. J. Immunol. Methods. 2008; 335: 21-7.</mixed-citation></ref><ref id="B22"><label>22.</label><mixed-citation>Guo X., Liu L., Zhang M. et al. Correlation of CD34+ cells with tissue angiogenesis after traumatic brain injury in a rat model. Neurotrauma 2009; 26: 1337-44.</mixed-citation></ref><ref id="B23"><label>23.</label><mixed-citation>Thau-Zuchman O., Shohami E., Alexandrovich A.G. et al. Vascular endothelial growth factor increases neurogenesis after traumatic brain injury. J. Cereb. Blood Flow Metabol. 2010; 30: 1008-16.</mixed-citation></ref><ref id="B24"><label>24.</label><mixed-citation>Padfield G.J., Tura O., Haeck M.L. et al. Circulating endothelial progenitor cells are not affected by acute systemic inflammation. Am. J. Physiol. Heart Circ. Physiol. 2010; 298: 2054-61.</mixed-citation></ref><ref id="B25"><label>25.</label><mixed-citation>Chen J., Sanberg P.R., Li Y. et al. Intravenous administration of human umbilical cord blood reduces behavioral deficits after stroke in rats. Stroke 2001. 32: 2682-8.</mixed-citation></ref><ref id="B26"><label>26.</label><mixed-citation>Taguchi A., Soma T., Tanaka H. et al. Administration of CD34+ cells after stroke enhances neurogenesis via angiogenesis in a mouse model. J. Clin. Invest. 2004; 114: 330-8.</mixed-citation></ref><ref id="B27"><label>27.</label><mixed-citation>Nan Z., Grande A., Sanberg C.D. et al. Infusion of human umbilical cord blood ameliorates neurologic deficits in rats with hemorrhagic brain injury. Ann. NY Acad. Sci. 2005; 1049: 84-96.</mixed-citation></ref><ref id="B28"><label>28.</label><mixed-citation>Bogoslovsky T., Chaudhry A., Latour L. et al. Endothelial progenitor cells correlate with lesion volume and growth in acute stroke. Neurology 2010; 75: 2059-62.</mixed-citation></ref><ref id="B29"><label>29.</label><mixed-citation>Taguchi A., Matsuyama T., Moriwaki H. et al. Circulating CD34- positive cells provide an index of cerebrovascular function. Circulation 2004; 109: 2972-5.</mixed-citation></ref></ref-list></back></article>
