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Flk1+ and VE-Cadherin+ Endothelial Cells Derived from iPSCs Recapitulates Vascular Development during Differentiation and Display Similar Angiogenic Potential as ESC-Derived Cells

机译:从iPSC衍生的Flk1 +和VE-钙黏着蛋白+内皮细胞概括了分化过程中的血管发育并显示了与ESC衍生细胞相似的血管生成潜能

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摘要

RationaleInduced pluripotent stem (iPS) cells have emerged as a source of potentially unlimited supply of autologous endothelial cells (ECs) for vascularization. However, the regenerative function of these cells relative to adult ECs and ECs derived from embryonic stem (ES) cells is unknown. The objective was to define the differentiation characteristics and vascularization potential of Fetal liver kinase (Flk)1+ and Vascular Endothelial (VE)-cadherin+ ECs derived identically from mouse (m)ES and miPS cells.
机译:基本原理诱导多能干(iPS)细胞已成为可能无限供应自体内皮细胞(EC)进行血管形成的来源。但是,这些细胞相对于成年EC和源自胚胎干(ES)细胞的EC的再生功能是未知的。目的是确定源自小鼠的胎肝激酶(Flk)1 + 和血管内皮(VE)-钙黏着蛋白 + EC的分化特征和血管形成潜力ES和miPS细胞。

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