LIF signal in mouse embryonic stem cells.

JAK-STAT Pub Date : 2015-09-11 eCollection Date: 2015-01-01 DOI:10.1080/21623996.2015.1086520
Satoshi Ohtsuka, Yoko Nakai-Futatsugi, Hitoshi Niwa
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引用次数: 51

Abstract

Since the establishment of mouse embryonic stem cells (mESCs) in the 1980s, a number of important notions on the self-renewal of pluripotent stem cells in vitro have been found. In serum containing conventional culture, an exogenous cytokine, leukemia inhibitory factor (LIF), is absolutely essential for the maintenance of pluripotency. In contrast, in serum-free culture with simultaneous inhibition of Map-kinase and Gsk3 (so called 2i-culture), LIF is no longer required. However, recent findings also suggest that LIF may have a role not covered by the 2i for the maintenance of naïve pluripotency. These suggest that LIF functions for the maintenance of naïve pluripotency in a context dependent manner. We summarize how LIF-signal pathway is converged to maintain the naïve state of pluripotency.

Abstract Image

Abstract Image

小鼠胚胎干细胞中的LIF信号。
自20世纪80年代小鼠胚胎干细胞(mESCs)建立以来,人们发现了许多关于体外多能干细胞自我更新的重要概念。在含有常规培养物的血清中,一种外源性细胞因子,白血病抑制因子(LIF),对于维持多能性是绝对必要的。相反,在同时抑制map -激酶和Gsk3的无血清培养(所谓的2i培养)中,不再需要LIF。然而,最近的研究结果也表明,LIF可能在维持naïve多能性方面具有2i未涵盖的作用。这表明,LIF以上下文依赖的方式维持naïve多能性。我们总结了lif信号通路如何收敛以维持naïve多能状态。
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