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<article article-type="research-article" dtd-version="1.3" 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" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">mimmun</journal-id><journal-title-group><journal-title xml:lang="ru">Медицинская иммунология</journal-title><trans-title-group xml:lang="en"><trans-title>Medical Immunology (Russia)</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1563-0625</issn><issn pub-type="epub">2313-741X</issn><publisher><publisher-name>SPb RAACI</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.15789/1563-0625-2010-1-2-7-12</article-id><article-id custom-type="elpub" pub-id-type="custom">mimmun-26</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>ОРИГИНАЛЬНЫЕ СТАТЬИ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>ORIGINAL ARTICLES</subject></subj-group></article-categories><title-group><article-title>РОЛЬ МАКРОФАГОВ В РЕГУЛЯЦИИ ПРОЦЕССА МИГРАЦИИ ЕМОПОЭТИЧЕСКИХ СТВОЛОВЫХ КЛЕТОК В СИСТЕМЕ КОСТНЫЙ МОЗГ – ПЕРИФЕРИЧЕСКАЯ КРОВЬ</article-title><trans-title-group xml:lang="en"><trans-title>ROLE OF MACROPHAGES IN REGULATION OF HEMATOPOIETIC STEM CELL MIGRATION IN BONE MARROW PERIPHERAL BLOOD SYSTEM</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Юшков</surname><given-names>Б. Г.</given-names></name><name name-style="western" xml:lang="en"><surname>Yushkov</surname><given-names>B. G.</given-names></name></name-alternatives><email xlink:type="simple">brykina_irina@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Данилова</surname><given-names>И. Г.</given-names></name><name name-style="western" xml:lang="en"><surname>Danilova</surname><given-names>I. G.</given-names></name></name-alternatives><email xlink:type="simple">brykina_irina@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Пашнина</surname><given-names>И. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Pashnina</surname><given-names>I. A.</given-names></name></name-alternatives><email xlink:type="simple">brykina_irina@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Брыкина</surname><given-names>И. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Brykina</surname><given-names>I. A.</given-names></name></name-alternatives><email xlink:type="simple">brykina_irina@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Абидов</surname><given-names>М. Т.</given-names></name><name name-style="western" xml:lang="en"><surname>Abidov</surname><given-names>M. T.</given-names></name></name-alternatives><email xlink:type="simple">brykina_irina@mail.ru</email><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru">Институт иммунологии и физиологии УрО РАН, г. Екатеринбург<country>Россия</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru">Институт иммунопатологии, Москва<country>Россия</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2010</year></pub-date><pub-date pub-type="epub"><day>07</day><month>07</month><year>2014</year></pub-date><volume>12</volume><issue>1-2</issue><fpage>7</fpage><lpage>12</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Юшков Б.Г., Данилова И.Г., Пашнина И.А., Брыкина И.А., Абидов М.Т., 2014</copyright-statement><copyright-year>2014</copyright-year><copyright-holder xml:lang="ru">Юшков Б.Г., Данилова И.Г., Пашнина И.А., Брыкина И.А., Абидов М.Т.</copyright-holder><copyright-holder xml:lang="en">Yushkov B.G., Danilova I.G., Pashnina I.A., Brykina I.A., Abidov M.T.</copyright-holder><license license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://www.mimmun.ru/mimmun/article/view/26">https://www.mimmun.ru/mimmun/article/view/26</self-uri><abstract><p>В настоящее время активно изучаются механизмы, обеспечивающие выход ГСК в циркуляцию и миграцию их к поврежденному органу. Исследуется участие макрофагов в данных процессах. В данном исследовании проведен цитофлюориметрический анализ содержания CD117+CD38+ и CD117+CD90low ГСК в периферической крови и костном мозге мышей при повреждения печени и почек на фоне стимуляции системы фагоцитирующих мононуклеаров препаратом тамерит. После частичной гепатотомии в костном мозге наблюдается увеличение содержания CD117+CD38+ ГСК, а введение тамерита стимулирует выход данных клеток в циркуляцию. При повреждении почки также отмечается возрастание уровня CD117+CD38+ ГСК в периферической крови мышей. При повреждении печени не обнаружено изменения содержания CD117+CD90low клеток ни в одной из исследуемых тканей, в то время как у нефротомированных мышей наблюдается рост уровня данных клеток в крови. Таким образом, стимуляция макрофагов оказывает разнонаправленное действие на CD117+CD38+ и CD117+CD90low популяцию ГСК. Согласно полученным данным, можно предположить, что мобилизация ГСК из костного мозга в кровь зависит в той или иной степени от системы фагоцитирующих мононуклеаров, и что стимуляция данной системы играет важную роль в регуляции процессов пролиферации и миграции различных популяций ГСК при повреждении печени и почек.</p></abstract><trans-abstract xml:lang="en"><p>Mechanisms by which HSCs mobilize into damaged organs are currently under scrutiny.Macrophage role in these processes is investigated. In this study, we performed a flow cytometry analysis ofCD117+CD38+ and CD117+CD90low HSCs quantity in murine peripheral blood and bone marrow after liverand kidney injury under stimulation of phagocyte mononuclear system by injection of tamerit. This study havedemonstrated increased levels of CD117+CD38+ HSCs in bone marrow after partial hepatectomy, along withtheir migration to peripheral blood in response to tamerit injection. We also demonstrated that peripheralblood CD117+CD38+ HSCs levels were elevated after kidney injury. After partial hepatectomy, nochangesof CD117+CD90low HSCs quantity in investigated tissues were detected. We observed increased number ofCD117+CD90low HSCs in murine blood following kidney injury. Thus, we observed different influence ofmacrophage stimulation on the quantity of CD117+CD38+ and CD117+CD90low cells. These data suggestthat HSCs mobilization from the bone marrow to peripheral blood depends, at least in part, on phagocytemononuclear system, and that macrophage stimulation is important for proliferation and migration of variousHSCs populations following liver and kidney injury.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>гемопоэтическая стволовая клетка</kwd><kwd>макрофаг</kwd><kwd>миграция</kwd><kwd>регенерация</kwd><kwd>тамерит</kwd></kwd-group><kwd-group xml:lang="en"><kwd>hematopoietic stem cell</kwd><kwd>macrophage</kwd><kwd>migration</kwd><kwd>regeneration</kwd><kwd>tamerit treatment</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Галактионов В.Г. Иммунология. – М.: Издательский центр «Академия», 2004. – 528 с.</mixed-citation><mixed-citation xml:lang="en">Галактионов В.Г. Иммунология. – М.: Издательский центр «Академия», 2004. – 528 с.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Козинец Г.И. Кровь и инфекция. – М.: Триада-Фарм, 2001. – 456 с.</mixed-citation><mixed-citation xml:lang="en">Козинец Г.И. Кровь и инфекция. – М.: Триада-Фарм, 2001. – 456 с.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Никитин И.Г. Стволовые клетки печени: современное состояние проблемы // Клинические перспективы гастроэнтерологии, гепатологии. – 2004. – № 3. – С. 10-15.</mixed-citation><mixed-citation xml:lang="en">Никитин И.Г. Стволовые клетки печени: современное состояние проблемы // Клинические перспективы гастроэнтерологии, гепатологии. – 2004. – № 3. – С. 10-15.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Новое в учении о регенерации / Под ред. Л.Д. Лиознера. – М.: Медицина, 1977. – 358 с.</mixed-citation><mixed-citation xml:lang="en">Новое в учении о регенерации / Под ред. Л.Д. Лиознера. – М.: Медицина, 1977. – 358 с.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Осипенко А.В., Черешнев В.А. Иммунобиологические механизмы регенерации тканей. – Екатеринбург: УрО РАН, 1997. – 130 с.</mixed-citation><mixed-citation xml:lang="en">Осипенко А.В., Черешнев В.А. Иммунобиологические механизмы регенерации тканей. – Екатеринбург: УрО РАН, 1997. – 130 с.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Регистр лекарственных средств России. Энциклопедия лекарств. Ежегодный сборник. Выпуск 9 / Под ред. Г.Л. Вышковского. – М.: ООО «РЛС», 2002. – 1504 с.</mixed-citation><mixed-citation xml:lang="en">Регистр лекарственных средств России. Энциклопедия лекарств. Ежегодный сборник. Выпуск 9 / Под ред. Г.Л. Вышковского. – М.: ООО «РЛС», 2002. – 1504 с.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Ройт А., Бростофф Дж., Мейл Д. Иммунология. – М.: Мир, 2000. – 592 с.</mixed-citation><mixed-citation xml:lang="en">Ройт А., Бростофф Дж., Мейл Д. Иммунология. – М.: Мир, 2000. – 592 с.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Хаитов Р.М. Физиология иммунной системы. – М., 2001. – 223 с.</mixed-citation><mixed-citation xml:lang="en">Хаитов Р.М. Физиология иммунной системы. – М., 2001. – 223 с.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Alison M.R., Poulsom R., Jeffery R.,Dhillon A.P., Quaglia A., Jacob J., Novelli M.,Prentice G., Williamson J., Writght N.A. Hepatocytes from non-hepatic adult stem cells // Nature. – 2000. – Vol. 406. – P. 257-260.</mixed-citation><mixed-citation xml:lang="en">Alison M.R., Poulsom R., Jeffery R.,Dhillon A.P., Quaglia A., Jacob J., Novelli M.,Prentice G., Williamson J., Writght N.A. Hepatocytes from non-hepatic adult stem cells // Nature. – 2000. – Vol. 406. – P. 257-260.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Dalakas E., Newsome P., Harrison D., Plevris J. Hematopoietic stem cell trafficking in liver injury // FASEB J. – 2005. – Vol. 19. – P. 1225-1231.</mixed-citation><mixed-citation xml:lang="en">Dalakas E., Newsome P., Harrison D., Plevris J. Hematopoietic stem cell trafficking in liver injury // FASEB J. – 2005. – Vol. 19. – P. 1225-1231.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Dawn B., Guo Y., Rezazadeh A. Postinfarct cytokine therapy regenerates cardiac tissue and improves left ventricular function // Circulation research. – 2006. – Vol. 98. – P. 1098-1105.</mixed-citation><mixed-citation xml:lang="en">Dawn B., Guo Y., Rezazadeh A. Postinfarct cytokine therapy regenerates cardiac tissue and improves left ventricular function // Circulation research. – 2006. – Vol. 98. – P. 1098-1105.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Ferrari G., Gusella-De Angelis G., Coletta M., Paolucci E., Stornaiuolo A., Cossu G., Mavilio F. Muscle regeneration by bone marrowderived myogenic progenitors // Science. – 1998. – Vol. 279. – P. 1528-1530.</mixed-citation><mixed-citation xml:lang="en">Ferrari G., Gusella-De Angelis G., Coletta M., Paolucci E., Stornaiuolo A., Cossu G., Mavilio F. Muscle regeneration by bone marrowderived myogenic progenitors // Science. – 1998. – Vol. 279. – P. 1528-1530.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Filip S., English D., Mokry J. Issues in stem cell plasticity // J. Cell. Mol. Med. – 2004. – Vol. 8 – P. 572-577.</mixed-citation><mixed-citation xml:lang="en">Filip S., English D., Mokry J. Issues in stem cell plasticity // J. Cell. Mol. Med. – 2004. – Vol. 8 – P. 572-577.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Hattori K., Heissig B., Tashiro K. Plasma elevation of stromal cell-derived factor-1 induces mobilization of mature and immature haematopoietic progenitors and stem cells // Blood. – 2001. –Vol. 97. – P. 3354-3360.</mixed-citation><mixed-citation xml:lang="en">Hattori K., Heissig B., Tashiro K. Plasma elevation of stromal cell-derived factor-1 induces mobilization of mature and immature haematopoietic progenitors and stem cells // Blood. – 2001. –Vol. 97. – P. 3354-3360.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Higgins G.M., Anderson R.M. Experimental pathology of the liver. I. Restoration of the liver following partial surgical removal // Arch. Path. – 1931. – Vol. 272. – P. 186-202.</mixed-citation><mixed-citation xml:lang="en">Higgins G.M., Anderson R.M. Experimental pathology of the liver. I. Restoration of the liver following partial surgical removal // Arch. Path. – 1931. – Vol. 272. – P. 186-202.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Kent D., Copley M., Benz C., Dykstra B., Bowie M., Eaves C. Regulation of hematopoietic stem cells by the steel factor / KIT signaling pathway // Clin. Cancer Res. – 2008. – Vol. 14 – P. 1926-1930.</mixed-citation><mixed-citation xml:lang="en">Kent D., Copley M., Benz C., Dykstra B., Bowie M., Eaves C. Regulation of hematopoietic stem cells by the steel factor / KIT signaling pathway // Clin. Cancer Res. – 2008. – Vol. 14 – P. 1926-1930.</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Krause D., Cantley L.G. Bone marrow plasticity revisited: protection or differentiation in the kidney tubule? // J. Clin. Invest. – 2005. – Vol. 115. – P. 1705-1708.</mixed-citation><mixed-citation xml:lang="en">Krause D., Cantley L.G. Bone marrow plasticity revisited: protection or differentiation in the kidney tubule? // J. Clin. Invest. – 2005. – Vol. 115. – P. 1705-1708.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Ogawa M., Matsuzaki Y., Nishikawa S.,Hayashi S., Kunisada T., Sudo T., Kina T.,Nakauchi H., Nishikawa S. Expression and function of c-kit in hemopoietic progenitor cells // J. Exp. Med. – 1991. – Vol. 174 – P. 63-71.</mixed-citation><mixed-citation xml:lang="en">Ogawa M., Matsuzaki Y., Nishikawa S.,Hayashi S., Kunisada T., Sudo T., Kina T.,Nakauchi H., Nishikawa S. Expression and function of c-kit in hemopoietic progenitor cells // J. Exp. Med. – 1991. – Vol. 174 – P. 63-71.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Petersen B.E., Bowen W.C., Patrene K.D., Mars W.M., Sullivan A.K., Murase N., Boggs S.S., Greenberger J.S., Goff J.P. Bone marrow as a potential source of hepatic oval cells // Science. –1999. – Vol. 284. – P. 1168-1170.</mixed-citation><mixed-citation xml:lang="en">Petersen B.E., Bowen W.C., Patrene K.D., Mars W.M., Sullivan A.K., Murase N., Boggs S.S., Greenberger J.S., Goff J.P. Bone marrow as a potential source of hepatic oval cells // Science. –1999. – Vol. 284. – P. 1168-1170.</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Poulsom R., Alison MR., Cook T., Jeffery R., Ryan E., Forbes S.J., Hunt T., Wyles S., Wright N.A. Bone marrow stem cells contribute to healing of the kidney // J. Am. Soc. Nephrol. – 2003. – Vol. 14. – P. 48-54.</mixed-citation><mixed-citation xml:lang="en">Poulsom R., Alison MR., Cook T., Jeffery R., Ryan E., Forbes S.J., Hunt T., Wyles S., Wright N.A. Bone marrow stem cells contribute to healing of the kidney // J. Am. Soc. Nephrol. – 2003. – Vol. 14. – P. 48-54.</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Randall T.D., Lund F.E., Howard M.C., Weissman I.L. Expression of murine CD38 defines a population of long-term reconstituting hematopoietic stem cells // Blood. – 1996. – Vol. 87 – P. 4057-4067.</mixed-citation><mixed-citation xml:lang="en">Randall T.D., Lund F.E., Howard M.C., Weissman I.L. Expression of murine CD38 defines a population of long-term reconstituting hematopoietic stem cells // Blood. – 1996. – Vol. 87 – P. 4057-4067.</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Randall T.D., Weissman I.L. Characterization of a population of cells in the bone marrow that phenotypically mimics hematopoietic stem cells: resting stem cells or mystery population? // Stem Cells. – 1998. – Vol. 16 – P. 38-48.</mixed-citation><mixed-citation xml:lang="en">Randall T.D., Weissman I.L. Characterization of a population of cells in the bone marrow that phenotypically mimics hematopoietic stem cells: resting stem cells or mystery population? // Stem Cells. – 1998. – Vol. 16 – P. 38-48.</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Ren X., Hu B., Colletti L. Stem cell factor and its receptor, c-kit, are important for hepatocyte proliferation in wild-type and tumor necrosis factor receptor-1 knockout mice after 70% hepatectomy // Surgery. – 2008. – Vol. 143. – P. 790-802.</mixed-citation><mixed-citation xml:lang="en">Ren X., Hu B., Colletti L. Stem cell factor and its receptor, c-kit, are important for hepatocyte proliferation in wild-type and tumor necrosis factor receptor-1 knockout mice after 70% hepatectomy // Surgery. – 2008. – Vol. 143. – P. 790-802.</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Reya T. Regulation of hematopoietic stem cell self-renewal // Recent. Prog. Horm. Res. – 2003. – Vol. 58 – P. 283-295.</mixed-citation><mixed-citation xml:lang="en">Reya T. Regulation of hematopoietic stem cell self-renewal // Recent. Prog. Horm. Res. – 2003. – Vol. 58 – P. 283-295.</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Serafini M., Dylla S.J., Oki M., Heremans Y., Tolar J., Jiang Y., Buckley S.M., Pelacho B., Burns T.C., Frommer S., Rossi D.J., Bryder D., Panoskaltsis-Mortari A., O’Shaughnessy M.J., Nelson-Holte M., Fine G.C., Weissman I.L., Blazar B.R., Verfaillie C.M. Hematopoietic reconstitution by multipotent adult progenitor cells: precursors to long-term hematopoietic stem cells // J. Exp. Med. – 2007. – Vol. 204. – P. 129-139.</mixed-citation><mixed-citation xml:lang="en">Serafini M., Dylla S.J., Oki M., Heremans Y., Tolar J., Jiang Y., Buckley S.M., Pelacho B., Burns T.C., Frommer S., Rossi D.J., Bryder D., Panoskaltsis-Mortari A., O’Shaughnessy M.J., Nelson-Holte M., Fine G.C., Weissman I.L., Blazar B.R., Verfaillie C.M. Hematopoietic reconstitution by multipotent adult progenitor cells: precursors to long-term hematopoietic stem cells // J. Exp. Med. – 2007. – Vol. 204. – P. 129-139.</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Stroo I., Stokman G., Teske G., Florquin S., Leemans J. Haematopoietic stem cell migration to the ischemic damaged kidney is not altered by manipulating the SDF-1/CXCR4-axis // Nephrol. Dial. Transplant. – 2009. – Vol. 24. – P. 2082-2088.</mixed-citation><mixed-citation xml:lang="en">Stroo I., Stokman G., Teske G., Florquin S., Leemans J. Haematopoietic stem cell migration to the ischemic damaged kidney is not altered by manipulating the SDF-1/CXCR4-axis // Nephrol. Dial. Transplant. – 2009. – Vol. 24. – P. 2082-2088.</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Uchida N., Weissman I.L. Searching for hematopoietic stem cells: evidence that Thy-l.1 low Lin- Sсa-1 + cells are the only stem cells in C57BL / Ka-Thy-l.1 bone marrow // J. Exp. Med. – 1992. – Vol. 175 – P. 175-184.</mixed-citation><mixed-citation xml:lang="en">Uchida N., Weissman I.L. Searching for hematopoietic stem cells: evidence that Thy-l.1 low Lin- Sсa-1 + cells are the only stem cells in C57BL / Ka-Thy-l.1 bone marrow // J. Exp. Med. – 1992. – Vol. 175 – P. 175-184.</mixed-citation></citation-alternatives></ref></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
