Resetting Human Naïve Pluripotency.

Genetics and Epigenetics Pub Date : 2016-08-04 eCollection Date: 2016-01-01 DOI:10.4137/GEG.S38093
Jifang Xiao, Daniel H Mai, Liangqi Xie
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引用次数: 6

Abstract

The rodent naive pluripotent state is believed to represent the preimplantation inner cell mass state of the developing blastocyst and can derive self-renewing pluripotent embryonic stem cells (ESCs) in vitro. Nevertheless, human ESCs exhibit epigenetic, metabolic, and transcriptomic characteristics more akin to primed pluripotent stem cells (PSCs) derived from the postimplantation epiblast. Understanding the genetic and epigenetic mechanisms that constrain human ESCs in the primed state is crucial for the human naive pluripotent state resetting and numerous applications in regenerative medicine. In this review, we begin by defining the naive and primed states in the murine model and compare the epigenetic characteristics of those states to the human PSCs. We also examine the various reprogramming schemes to derive the human naive pluripotent state. Finally, we discuss future perspectives of studying and deriving the human naive PSCs in the context of cellular engineering and regenerative medicine.

重置人类Naïve多能性。
啮齿类动物的幼稚多能状态被认为是发育囊胚着床前的内细胞团状态,可以在体外获得自我更新的多能胚胎干细胞(ESCs)。然而,人类ESCs表现出的表观遗传学、代谢学和转录组学特征更类似于源自刺激后外胚层的多能干细胞(PSCs)。了解限制人类ESCs处于启动状态的遗传和表观遗传机制对于人类初始多能状态重置和在再生医学中的众多应用至关重要。在这篇综述中,我们首先定义了小鼠模型中的初始状态和启动状态,并将这些状态与人类psc的表观遗传特征进行了比较。我们还研究了各种重编程方案来推导人类幼稚多能状态。最后,我们讨论了在细胞工程和再生医学的背景下研究和获得人类原始psc的未来前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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