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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="other" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Annals of the Russian academy of medical sciences</journal-id><journal-title-group><journal-title xml:lang="en">Annals of the Russian academy of medical sciences</journal-title><trans-title-group xml:lang="ru"><trans-title>Вестник Российской академии медицинских наук</trans-title></trans-title-group></journal-title-group><issn publication-format="print">0869-6047</issn><issn publication-format="electronic">2414-3545</issn><publisher><publisher-name xml:lang="en">"Paediatrician" Publishers LLC</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">149</article-id><article-id pub-id-type="doi">10.15690/vramn.v68i9.779</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>SHORT MESSAGES</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>КРАТКИЕ СООБЩЕНИЯ</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">RECENT ADVANCES IN THE STUDY OF THE STEM CELLS MIGRATION METHODS</article-title><trans-title-group xml:lang="ru"><trans-title>СОВРЕМЕННЫЕ ДОСТИЖЕНИЯ В СОЗДАНИИ МЕТОДОВ ИЗУЧЕНИЯ МИГРАЦИИ СТВОЛОВЫХ КЛЕТОК</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Poveshchenko</surname><given-names>A. F.</given-names></name><name xml:lang="ru"><surname>Повещенко</surname><given-names>А. Ф.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>PhD, Head of the laboratory of protective system physiology of the Federal State Budgetary Institution «Scientific Research Institute of clinical and experimental lymphology» under the Siberian Branch of RAMS. Address: 2, Timakova St., Novosibirsk, 630117; tel.: (383) 333-64-09</p></bio><email>poveshchenkoa200@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Poveshchenko</surname><given-names>O. V.</given-names></name><name xml:lang="ru"><surname>Повещенко</surname><given-names>О. В.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>MD, Head of the lymphotropic therapy and lymphodiagnostic laboratory of the Federal State Budgetary Institution «Scientific Research Institute of clinical and experimental lymphology» under the Siberian Branch of RAMS. Address: 2, Timakova St., Novosibirsk, 630117; tel.: (383) 333-64-09</p></bio><email>poveshchenkoa200@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Konenkov</surname><given-names>V. I.</given-names></name><name xml:lang="ru"><surname>Коненков</surname><given-names>В. И.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>PhD, professor, member of the RAMS, director of the Federal State Budgetary Institution «Scientific Research Institute of clinical and experimental lymphology» under the Siberian Branch of RAMS. Address: 2, Timakova St., Novosibirsk, 630117; tel.: (383) 333-64-09</p></bio><email>lymphology@soramn.ru</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Scientific Institution of Clinical and Experimental Lymphology of the Siberian Branch, RAMS, Novosibirsk, Russian Federation</institution></aff><aff><institution xml:lang="ru">НИИ клинической и экспериментальной лимфологии СО РАМН, Новосибирск, Российская Федерация</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2013-09-10" publication-format="electronic"><day>10</day><month>09</month><year>2013</year></pub-date><volume>68</volume><issue>9</issue><issue-title xml:lang="en">Vestnik Rossiiskoi akademii medetsinskikh nauk / Annals of the Russian academy of medical sciences</issue-title><issue-title xml:lang="ru">Вестник Российской академии медицинских наук</issue-title><fpage>46</fpage><lpage>51</lpage><history><date date-type="received" iso-8601-date="2015-08-07"><day>07</day><month>08</month><year>2015</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 1970, "Paediatrician" Publishers LLC</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 1970, Издательство "Педиатръ"</copyright-statement><copyright-year>1970</copyright-year><copyright-holder xml:lang="en">"Paediatrician" Publishers LLC</copyright-holder><copyright-holder xml:lang="ru">Издательство "Педиатръ"</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://vestnikramn.spr-journal.ru/jour/about/submissions</ali:license_ref></license></permissions><self-uri xlink:href="https://vestnikramn.spr-journal.ru/jour/article/view/149">https://vestnikramn.spr-journal.ru/jour/article/view/149</self-uri><abstract xml:lang="en"><p><italic>Review is devoted to</italic><italic> a comparative analysis of stem cells migration methods for studying in experimental conditions and clinics, assessing their strengths and weaknesses. It is impossible to single out any one preferred method for studying the migration of stem cells. Each method has its own set of advantages and disadvantages. X-ray methods " suffer" from non-specific binding of contrast marks, followed by rapid degradation and the release of the body. If it is necessary to study the migration of the transplanted stem cells for a long time interval, the visualization of the reporter gene is the best available techniques, since it can provide a non-invasive real time monitoring of the location in the tissue and stem cells isolated help assess their viability and proliferation. The most attractive of the agents for monitoring - endogenous, i.e. natural constituents stem cells, for example, genetic markers. Criteria for the application of methods to study migration in clinical and experimental results have significant differences. The main criteria for the methods of the study of cell migration in clinical settings, it must be biocompatible, safe, non-toxic, non-invasive. Accordingly, the main criteria for the experimental methods for studying the migration will be accuracy, the ability to quantify the long-term migration of cells and stability of the "label".</italic><italic/></p></abstract><trans-abstract xml:lang="ru"><p><italic>Обзор посвящен сравнительному анализу методов исследования миграции стволовых клеток в условиях эксперимента и клиники, оценке их преимуществ и недостатков. </italic><italic>Невозможно выделить какой-то один преимущественный метод исследования миграции стволовых клеток, идеальный во всех аспектах. Каждый из методов имеет свой набор достоинств и недостатков. Рентгенологические методы «страдают» неспецифическим связыванием контрастной метки с последующей быстрой деградацией и выделением из организма. Если необходимо изучить миграцию трансплантированных стволовых клеток в течение длительного временного интервала, то визуализация гена-репортера является наилучшим из имеющихся методов, поскольку она может обеспечить неинвазивный мониторинг в реальном времени расположения в тканях организма единичных стволовых клеток и помочь оценить их жизнеспособность и пролиферацию. Наиболее привлекательны из агентов для отслеживания — эндогенные, т.е. природные составляющие стволовых клеток, например, генетические маркеры. Критерии для применения методов изучения миграции в условиях клиники и эксперимента имеют существенные различия. Главными критериями для методов исследования миграции клеток в клинических условиях, очевидно, должны быть биосовместимость, безопасность, нетоксичность, неинвазивность. Соответственно, основными критериями для экспериментальных методов изучения миграции будут точность, возможность длительной количественной оценки миграции клеток и стабильность «метки».</italic></p><p> </p></trans-abstract><kwd-group xml:lang="en"><kwd>stem cells</kwd><kwd>migration</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>стволовые клетки</kwd><kwd>миграция</kwd></kwd-group><funding-group/></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>1.	Till J.E., McCulloch E.A. A direct measurement of the radiation sensitivity of normal mouse bone marrow cells. Radist. Res. 1961; 14 (2):213–222.</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>2.	Petrov R.V., Khaitov R.M. Migration of stem cells from the bone marrow shielded with uneven exposure. Radiobiologiya = Radiobiology. 1972; 12(1): 69–76.</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>3.	Frangioni J.V., Hajjar R.J. In vivo tracking of stem cells for clinical trials in cardiovascular disease. Circulation. 2004; 110: 3378–3384.</mixed-citation></ref><ref id="B4"><label>4.</label><mixed-citation>4.	Torrente, Y., Gavina, M., Belicchi, M., Fiori F, Komlev V., Bresolin N., Rustichelli F. X-ray microtomography for three-dimensional visualization of human stem cell muscle homing. FEBS Lett. 2006; 580(24): 5759–5764.</mixed-citation></ref><ref id="B5"><label>5.</label><mixed-citation>5.	Detante, O., Moisan A., Dimastromatteo J.,Richard M.J., Riou L., Grillon E., Barbier E., Desruet M.D., DeFraipont F, Segebarth C., Jaillard A., Hommel M., Ghezzi C., Remy C. Intravenous administration of 99mTc-HMPAO-labeled human mesenchymal stem cells after stroke: in vivo imaging and biodistribution. Cell Transplant. 2009; 18 (12): 1369–1379.</mixed-citation></ref><ref id="B6"><label>6.</label><mixed-citation>6.	Gholamrezanezhad, A., Mirpour S., Bagheri M., Mohamadnejad M., Alimoghaddam K., Abdolahzadeh L., Saghari M., Malekzadeh R. .In vivo tracking of 111In-oxine labeled mesenchymal stem cells following infusion in patients with advanced cirrhosis. Nucl. Med. &amp; Biol. 2011; 38 (7): 961–967.</mixed-citation></ref><ref id="B7"><label>7.</label><mixed-citation>7.	Kang W.J., Kang H.J., Kim H.S.,Chung J.K.,Lee M.C., Lee D.S. Tissue distribution of 18F-FDG-labeled peripheral hematopoietic stem cells after intracoronary administration in patients with myocardial infarction. J. Nucl. Med. 2006; 47 (8): 1295–1301.</mixed-citation></ref><ref id="B8"><label>8.</label><mixed-citation>8.	Ramot Y., Steiner M., Morad V., Leibovitch S., Amouyal N., Cesta M.F., Nyska A. et al. Pulmonary thrombosis in the mouse following intravenous administration of quantum dot-labeled mesenchymal cells. Nanotoxicology. 2010; 4(1): 98–105.</mixed-citation></ref><ref id="B9"><label>9.</label><mixed-citation>9.	Michalet X., Pinaud F.F., Bentolila L.A., Tsay JM, Doose S, Li JJ, Sundaresan G, Wu AM, Gambhir SS, Weiss S. Quantum dots for live cells, in vivo imaging, and diagnostics. Science. 2005; 307(5709): 538–544.</mixed-citation></ref><ref id="B10"><label>10.</label><mixed-citation>10.	Shah B.S. Clark P.A. Moioli, E.K., Stroscio MA, Mao JJ. Labeling of mesenchymal stem cells by bioconjugated quantum dots. Nano Lett. 2007; 7(10): 3071–3079.</mixed-citation></ref><ref id="B11"><label>11.</label><mixed-citation>11.	Slotkin J.R., Chakrabarti, L., Dai, H.N. Carney RS, Hirata T, Bregman BS, Gallicano GI, Corbin JG, Haydar TF.. In vivo quantum dot labeling of mammalian stem and progenitor cells. Dev. Dyn. 2007; 236(12): 3393–3401.</mixed-citation></ref><ref id="B12"><label>12.</label><mixed-citation>12.	Gera A., Steinberg G.K., Guzman R. In vivo neural stem cell imaging: current modalities and future directions. Regenerative Medicine. 2010; 5 (1): 73–86.</mixed-citation></ref><ref id="B13"><label>13.</label><mixed-citation>13.	Villa C., Erratico S., Razini P., Fiori F., Rustichelli F., Torrente Y., Belicchi M. Stem cell tracking by nanotechnologies. Int. J. Mol. Sci. 2010; 11(3): 1070–1081.</mixed-citation></ref><ref id="B14"><label>14.</label><mixed-citation>14.	Kustermann E., Roell W., Breitbach M., Wecker S, Wiedermann D., Buehrle C., Welz A., Hescheler J., Fleischmann BK, Hoehn M. Stem cell implantation in ischemic mouse heart: a high-resolution magnetic resonance imaging investigation. NMR Biomed. 2005; 18(6): 362–370.</mixed-citation></ref><ref id="B15"><label>15.</label><mixed-citation>15.	Walczak P., Zhang J., Gilad A.A., Kedziorek D.A., Ruiz-Cabello J., Young R.G., Pittenger M.F., van Zijl P.C., Huang J., Bulte J.W. Dual-modality monitoring of targeted intraarterial delivery of mesenchymal stem cells after transient ischemia. Stroke. 2008; 39(5): 1569–1574.</mixed-citation></ref><ref id="B16"><label>16.</label><mixed-citation>16.	Himmelreich U., Hoehn M. Stem cell labeling for magnetic resonance imaging. Minim. Invasive Ther. Allied Technol. 2008; 17: 132–142.</mixed-citation></ref><ref id="B17"><label>17.</label><mixed-citation>17.	Kraitchman D.L., Bulte J.W. In vivo imaging of stem cells and Beta cells using direct cell labeling and reporter gene methods. Arterioscler. Thromb. Vasc. Biol. 2009; 29 (7): 1025–1030.</mixed-citation></ref><ref id="B18"><label>18.</label><mixed-citation>18.	Modo M., Cash, D., Mellodew K. Williams SC, Fraser SE, Meade TJ, Price J, Hodges H. Tracking transplanted stem cell migration using bifunctional, contrast agent-enhanced, magnetic resonance imaging. Neuroimage. 2002; 17(2): 803–811.</mixed-citation></ref><ref id="B19"><label>19.</label><mixed-citation>19.	Higuchi T., Anton M., Dumler K., Seidl S, Pelisek J, Saraste A, Welling A, Hofmann F, Oostendorp RA, Gansbacher B, Nekolla SG, Bengel FM, Botnar RM, Schwaiger M. Combined reporter gene PET and iron oxide MRI for monitoring survival and localization of transplanted cells in the rat heart. J. Nucl. Med. 2009; 50 (7): 1088–1094.</mixed-citation></ref><ref id="B20"><label>20.</label><mixed-citation>20.	Kasinskaya N.V., Stepanova O.I., Karkishchenko N.N., Karkishchenko V.N., Semenov Kh.Kh., Beskova T.B., Kapanadze G.D., Revyakin A.O., Dengina S.E. Green protein gene as a marker in the transplantation of stem and progenitor cells in the bone marrow. Biomeditsina = Biomedicine. 2011; 2: 30–34.</mixed-citation></ref><ref id="B21"><label>21.</label><mixed-citation>21.	Reumers V., Deroose C.M., Krylyshkina O., Nuyts J, Geraerts M, Mortelmans L, Gijsbers R, Van den Haute C, Debyser Z, Baekelandt V.Noninvasive and quantitative monitoring of adult neuronal stem cell migration in mouse brain using bioluminescence imaging. Stem Cells. 2008; 26 (9): 2382–2390.</mixed-citation></ref><ref id="B22"><label>22.</label><mixed-citation>22.	Zhang H.L., Qiao H., Bakken A., Gao F, Huang B, Liu YY, El-Deiry W, Ferrari VA, Zhou R. Utility of dual-modality bioluminescence and MRI in monitoring stem cell survival and impact on post myocardial infarct. Remodeling Acad. Radiol. 2011; 18 (1): 3–12.</mixed-citation></ref><ref id="B23"><label>23.</label><mixed-citation>23.	Zhang S.J., Wu J.C. Comparison of imaging techniques for tracking cardiac stem cell therapy. J. Nucl. Med. 2007; 48 (12): 1916–1919.</mixed-citation></ref><ref id="B24"><label>24.</label><mixed-citation>24.	Polzer H., Haaster F.S., Prall W.C., Saller MM, Volkmer E, Drosse I, Mutschler W, Schieker M. Quantification of fluorescence intensity of labeled human mesenchymal stem cells and cell counting of unlabeled cells in phase-contrast imaging: An open-source-based algorithm. Tis. Engineering Part C Meth. 2010; 16 (6); 1277–1285.</mixed-citation></ref><ref id="B25"><label>25.</label><mixed-citation>25.	Sung C.K., Hong K.A., Lin S. Lee Y, Cha J, Lee JK, Hong CP, Han BS, Jung SI, Kim SH, Yoon KS. Dual-modal nanoprobes for imaging of mesenchymal stem cell transplant by MRI and fluorescence imaging. Korean J. Radiol. 2009; 10 (6): 613–622.</mixed-citation></ref></ref-list></back></article>
