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									<identifier>oai:www.peertechzpublications.org:10.17352/sscrt.000006</identifier>
									<datestamp>2016-11-29</datestamp>
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									<oai_dc:dc xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:mml="http://www.w3.org/1998/Math/MathML" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
										<dc:title>
										Cytokine Production by Circulating Endothelial Progenitor Cells before and after G-CSF Mobilization
										</dc:title><dc:creator>Alexander Lykov</dc:creator><dc:creator> Olga  Poveschenko</dc:creator><dc:creator> Natalia  Bondarenko</dc:creator><dc:creator> Alexander  Poveschenko</dc:creator><dc:creator> Irina Kim</dc:creator><dc:creator> Eugenie  Pokushalov</dc:creator><dc:creator> Alexander Romanov </dc:creator><dc:creator>Vladimir Konenkov</dc:creator><dc:description>&lt;p&gt;&lt;strong&gt;Objective: &lt;/strong&gt;Bone marrow-derived circulating endothelial cells (EPCs) may migrate in ischemia zone, to stimulate resident progenitor cells to proliferation, differentiation and migration in a damage zone, and reduce an ischemia zone through formation of new vessels. Granulocyte colony stimulating factor (G- &amp;nbsp; CSF) is well established to mobilize hematopoietic stem cells and might, thereby, also increase the pool of endogenously circulating EPCs. EPCs secrete pro-angiogenic factors. Therefore, we investigated the effects of G-CSF administration on mobilization and functional activities of bloodderived EPC in patients with chronic ischemic heart disease (CIHD).&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Methods and Results: &lt;/strong&gt;Ten patients with CIHD receive 300 μg per day subcutaneous G-CSF injection for 5 days. The number of EPCs, colony-forming capacity, tube formation and cytokine release were analyzed before and after G-CSF therapy. At day 5 of G-CSF treatment, the number of circulating CD34+CD45- and CD34+CD133+ and CD34+KDR+ cells significantly increased in patients with CIHD. Also, G-CSF therapy augmented the colony-forming capacity and tube formation by EPCs. Likewise, G-CSF treatment augmented cytokine production by circulating EPCs. Early EPCs and late EPCs produced a wide range of cytokines, which dependent the culture condition (gelatin-loaded or fibronectin-loaded surface of culture flask) and the days of cultivation (on day 8 or on day 16). &lt;br&gt;&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Conclusion:&lt;/strong&gt; G-CSF treatment effectively mobilizes EPCs, which through paracrine factors production may influence at the resident progenitor cells in ischemic zone of heart to stimulate the repair of myocardium through neoangiogenesis.&lt;/p&gt;</dc:description>
										<dc:publisher>Studies on Stem Cells Research and Therapy - Peertechz Publications</dc:publisher>
										<dc:date>2016-11-29</dc:date>
										<dc:type>Research Article</dc:type>
										<dc:identifier>https://doi.org/10.17352/sscrt.000006</dc:identifier>
										<dc:language>en</dc:language>
										<dc:rights>Copyright © Alexander Lykov et al.</dc:rights>
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