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转录因子介导的重编程为多能性的十年。

A decade of transcription factor-mediated reprogramming to pluripotency.

机构信息

Center for iPS Cell Research and Application, Kyoto University, Kyoto, 606-8507, Japan, and the Gladstone Institute of Cardiovascular Disease, University of California, San Francisco, California 94158, USA.

出版信息

Nat Rev Mol Cell Biol. 2016 Mar;17(3):183-93. doi: 10.1038/nrm.2016.8. Epub 2016 Feb 17.

Abstract

The past 10 years have seen great advances in our ability to manipulate cell fate, including the induction of pluripotency in vitro to generate induced pluripotent stem cells (iPSCs). This process proved to be remarkably simple from a technical perspective, only needing the host cell and a defined cocktail of transcription factors, with four factors - octamer-binding protein 3/4 (OCT3/4), SOX2, Krüppel-like factor 4 (KLF4) and MYC (collectively referred to as OSKM) - initially used. The mechanisms underlying transcription factor-mediated reprogramming are still poorly understood; however, several mechanistic insights have recently been obtained. Recent years have also brought significant progress in increasing the efficiency of this technique, making it more amenable to applications in the fields of regenerative medicine, disease modelling and drug discovery.

摘要

在过去的 10 年中,我们在操纵细胞命运方面取得了重大进展,包括在体外诱导多能性以产生诱导多能干细胞(iPSCs)。从技术角度来看,这个过程非常简单,只需要宿主细胞和一组定义明确的转录因子,最初使用的是四个因子 - 八聚体结合蛋白 3/4(OCT3/4)、SOX2、Krüppel 样因子 4(KLF4)和 MYC(统称为 OSKM)。转录因子介导的重编程的机制仍然知之甚少;然而,最近已经获得了一些机制上的见解。近年来,这项技术的效率也有了显著提高,使其更适用于再生医学、疾病建模和药物发现等领域的应用。

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