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Induced Differentiation of Human Cord Blood Mesenchymal Stem/Progenitor Cells into Cardiomyocyte-like Cells In Vitro

机译:诱导人脐带血间充质干细胞/祖细胞体外分化为心肌样细胞

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The feasibility of using cord blood mesenchymal stem/progenitor cells (CB-MSPCs) to regenerate cardiomyocytes and the optimal inducing conditions were investigated. The CB mononuclear cells were cultured in low serum DMEM medium to produce an adherent layer. After expansion, the adherent cells were added into cardiomyocyte inducing medium supplemented with 5-azacytidine. Cardiogenic specific contractile protein troponin T staining was performed to identify the cardiomy-ocyte-like cells. The results showed that the frequency of CB-MSPCs clones in CB mononuclear cells was 0. 5 X 10~(-6) and about 1. 3 X 10~7-fold expansion was achieved within 20 sub-cultivation. After car-diogenic induction, 70% CB-MSPCs was differentiated into cardiomyocyte-like cells. It was indicated that low serum culture could expand CB-MSPCs extensively and the expanded CB-MSPCs could be induced to differentiate into cardiomyocyte-like cells in high efficiency.
机译:研究了使用脐血间充质干/祖细胞(CB-MSPCs)再生心肌细胞的可行性和最佳诱导条件。在低血清DMEM培养基中培养CB单核细胞,以产生粘附层。扩增后,将贴壁细胞添加到补充有5-氮胞苷的心肌细胞诱导培养基中。进行心源性特异性收缩蛋白肌钙蛋白T染色,以鉴定心肌细胞样细胞。结果表明,CB-MSPCs克隆在CB单核细胞中的频率为0. 5 X 10〜(-6),在20次传代培养中扩增约1. 3 X 10〜7倍。致癌诱导后,70%的CB-MSPCs分化为心肌样细胞。结果表明,低血清培养可以使CB-MSPCs广泛扩增,并且可以诱导扩增后的CB-MSPCs高效分化为心肌样细胞。

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