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Time-course transcriptome analysis of human cellular reprogramming from multiple cell types reveals the drastic change occurs between the mid phase and the late phase

机译:从多种细胞类型对人类细胞进行重编程的时程转录组分析显示在中期和晚期之间发生了巨大变化

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摘要

BackgroundHuman induced pluripotent stem cells (hiPSCs) have been attempted for clinical application with diverse iPSCs sources derived from various cell types. This proposes that there would be a shared reprogramming route regardless of different starting cell types. However, the insights of reprogramming process are mostly restricted to only fibroblasts of both human and mouse. To understand molecular mechanisms of cellular reprogramming, the investigation of the conserved reprogramming routes from various cell types is needed. Particularly, the maturation, belonging to the mid phase of reprogramming, was reported as the main roadblock of reprogramming from human dermal fibroblasts to hiPSCs. Therefore, we investigated first whether the shared reprogramming routes exists across various human cell types and second whether the maturation is also a major blockage of reprogramming in various cell types.
机译:背景技术已尝试将人类诱导的多能干细胞(hiPSC)与源自各种细胞类型的多种iPSC来源进行临床应用。这建议不管起始单元格类型如何,都将存在共享的重编程路由。但是,重编程过程的见解大多仅限于人和小鼠的成纤维细胞。为了了解细胞重编程的分子机制,需要研究各种细胞类型的保守重编程途径。特别地,属于重编程中间阶段的成熟被报道为从人真皮成纤维细胞向hiPSCs重编程的主要障碍。因此,我们首先研究了在各种人类细胞类型之间是否存在共享的重编程途径,其次研究了成熟是否也是在各种细胞类型中重编程的主要障碍。

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