JAK-STAT3 and somatic cell reprogramming.

JAK-STAT Pub Date : 2013-10-01 Epub Date: 2013-05-07 DOI:10.4161/jkst.24935
Yong Tang, Xiuchun Cindy Tian
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引用次数: 35

Abstract

Reprogramming somatic cells to pluripotency, especially by the induced pluripotent stem cell (iPSC) technology, has become widely used today to generate various types of stem cells for research and for regenerative medicine. However the mechanism(s) of reprogramming still need detailed elucidation, including the roles played by the leukemia inhibitory factor (LIF) signaling pathway. LIF is central in maintaining the ground state pluripotency of mouse embryonic stem cells (ESCs) and iPSCs by activating the Janus kinase-signal transducer and activator of transcription 3 (JAK-STAT3) pathway. Characterizing and understanding this pathway holds the key to generate naïve pluripotent human iPSCs which will facilitate the development of patient-specific stem cell therapy. Here we review the historical and recent developments on how LIF signaling pathway regulates ESC pluripotency maintenance and somatic cell reprogramming, with a focus on JAK-STAT3.

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JAK-STAT3与体细胞重编程。
通过诱导多能干细胞(iPSC)技术对体细胞进行重编程使其具有多能性,目前已被广泛用于产生各种类型的干细胞,用于研究和再生医学。然而,重编程的机制仍需要详细阐明,包括白血病抑制因子(LIF)信号通路所起的作用。LIF通过激活Janus激酶信号转导因子和转录激活因子3 (JAK-STAT3)通路,在维持小鼠胚胎干细胞(ESCs)和iPSCs的基态多能性方面发挥着核心作用。表征和理解这一途径是生成naïve多能人类iPSCs的关键,这将促进患者特异性干细胞治疗的发展。本文综述了LIF信号通路调控ESC多能性维持和体细胞重编程的历史和最新进展,重点介绍了JAK-STAT3。
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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