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Production of endothelial progenitor cells obtained from human Wharton's jelly using different culture conditions

机译:使用不同培养条件,从人荷子果冻获得的内皮祖细胞的生产

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Endothelial progenitor cells (EPC) participate in revascularization and angiogenesis. EPC can be cultured in vitro from mononuclear cells of peripheral blood, umbilical cord blood or bone marrow; they also can be transdifferentiated from mesenchymal stem cells (MSC). We isolated EPCs from Wharton's jelly (WJ) using two methods. The first method was by obtaining MSC from WJ and characterizing them by flow cytometry and their adipogenic and osteogenic differentiation, then applying endothelial growth differentiating media. The second method was by direct culture of cells derived from WJ into endothelial differentiating media. EPCs were characterized by morphology, Dil-LDL uptake/UEA-1 immunostaining and testing the expression of endothelial markers by flow cytometry and RT-PCR. We found that MSC derived from WJ differentiated into endothelial-like cells using simple culture conditions with endothelium induction agents in the medium.
机译:内皮祖细胞(EPC)参与血运重建和血管生成。 EPC可以在外周血,脐带血或骨髓的单核细胞中体外培养; 它们还可以从间充质干细胞(MSC)转置。 我们使用两种方法从沃顿果冻(WJ)中孤立EPCS。 第一种方法是通过从WJ获得MSC并通过流式细胞术及其脂肪酸和骨质发生分化表征它们,然后施加内皮生长分化介质。 第二种方法是通过将衍生自WJ的细胞的直接培养为内皮分化培养基。 通过形态学,DIL-LDL摄取/ UEA-1免疫染色和测试内皮标记物的表达,通过流式细胞术和RT-PCR表征EPC。 我们发现,使用简单的培养条件与培养基中的内皮诱导剂的简单培养条件衍生自Wj的MSC。

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