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A comparison of the pro-angiogenic potential of human induced pluripotent stem cell derived endothelial cells and induced endothelial cells in a murine model of peripheral arterial disease

机译:人诱导多能干细胞衍生内皮细胞的促血管生成潜力的比较和外周动脉疾病小鼠模型中诱导内皮细胞的诱导内皮细胞

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Background: Endothelial cells derived from human induced pluripotent stem cells (iPSC-ECs) promote angiogen-esis, and more recently induced endothelial cells (iECs) have been generated via fibroblast trans-differentiation. These cell types have potential as treatments for peripheral arterial disease (PAD). However, it is unknown whether different reprogramming methods produce cells that are equivalent in terms of their pro-angiogenic capabilities. Objectives: We aimed to directly compare iPSC-ECs and iECs in an animal model of PAD, in order to identify which cell type, if any, displays superior therapeutic potential. Methods: IPSC-ECs and iECs were generated from human fibroblasts, and transduced with a reporter construct encoding GFP and firefly luciferase for bioluminescence imaging (BLI). Endothelial phenotype was confirmed using in vitro assays. NOD-SCID mice underwent hindlimb ischaemia surgery and received an intramuscular injection of either 1 x 106 iPSC-ECs, 1 x 106 iECs or control vehicle only. Perfusion recovery was measured by laser Doppler. Hindlimb muscle samples were taken for histological analyses.
机译:背景技术衍生自人诱导的多能干细胞(IPSC-ECS)的内皮细胞促进血管生成血管生成,并且通过成纤维细胞反分化产生了更最近诱导的内皮细胞(IECS)。这些细胞类型具有作为外周动脉疾病(PAD)的治疗。然而,尚不清楚不同的重编程方法是否产生在促血管生成能力方面等同的细胞。目标:我们的目标是直接将IPSC-EC和IECS与垫的动物模型进行比较,以确定哪种细胞类型(如果有的话)显示出优异的治疗潜力。方法:从人成纤维细胞产生IPSC-ECS和IEC,并用编码GFP和萤火虫荧光素酶的报告构建体转导,用于生物发光成像(BLI)。使用体外测定确认内皮表型。 NOD-SCID小鼠接受了后肢缺血手术,并仅接受了1×10 6 IPSC-EC,1×106 IECS或控制车辆的肌内注射。激光多普勒测量灌注恢复。 Hindlimb肌肉样品被​​用于组织学分析。

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