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Potentially immunogenic proteins expressed similarly in human embryonic stem cells and induced pluripotent stem cells

机译:潜在的免疫原性蛋白在人类胚胎干细胞和诱导性多能干细胞中表达相似

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A major limitation of the use of cellular therapies is the loss of donor-derived cells because of immune incompatibility. While induced pluripotent stem (iPS) cells offer the potential for autologous transplant therapies, questions have been raised using a mouse model that specific antigens mediate the rejection of grafts after syngeneic transplants with iPS, but not embryonic stem (ES) cells. In this study, we examined whether the human homologs of these markers, HORMAD1, ZG16, and Cyp3A, are differentially expressed in human iPS versus ES cells, as well as undifferentiated and in vitro-differentiated cells. Both qRT-PCR and flow cytometric analyses demonstrated similar gene and protein expression profiles for iPS and ES cells regardless of differentiation state. Our data are consistent with a recent study in mice that showed no evidence of rejection of differentiated syngeneic iPS cells. Furthermore, our results suggest that expression of these gene products cannot predict differences in clinical outcomes between human iPS and ES-derived cells.
机译:使用细胞疗法的主要限制是由于免疫不相容性而导致的供体来源细胞的损失。尽管诱导多能干(iPS)细胞为自体移植治疗提供了潜力,但使用小鼠模型提出了一个问题,即与iPS同基因移植后,特定抗原介导移植物的排斥反应,但胚胎干细胞(ES)没有。在这项研究中,我们检查了这些标记物HORMAD1,ZG16和Cyp3A的人类同源物是否在人iPS与ES细胞以及未分化和体外分化的细胞中差异表达。 qRT-PCR和流式细胞仪分析均显示了iPS和ES细胞的相似基因和蛋白质表达谱,而与分化状态无关。我们的数据与最近在小鼠中进行的研究一致,该研究没有证据显示分化的同系iPS细胞被排斥。此外,我们的结果表明,这些基因产物的表达不能预测人iPS和ES衍生细胞之间临床结果的差异。

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