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Kruppel-like Factor 4 (Klf4) Prevents Embryonic Stem (ES) Cell Differentiation by Regulating Nanog Gene Expression*

机译:Kruppel样因子4(Klf4)通过调节Nanog基因表达来防止胚胎干(ES)细胞分化*

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摘要

Transcription factor Kruppel-like factor 4 (Klf4) is essential for somatic cell reprogramming. In addition, Klf4 seems to play a redundant role along with other Klf family proteins in embryonic stem (ES) cell self-renewal. However, how Klf4 regulates ES cell self-renewal and somatic cell reprogramming is still poorly understood. Here we report that Klf4 is required for both ES cell self-renewal and maintenance of pluripotency and that the expression of Klf4 prevents ES cell differentiation in response to withdrawal of leukemia inhibitory factor (LIF) or bone morphogenetic protein 4 (BMP4). In addition, Klf4 directly binds to the promoter region of Nanog and regulates its expression. Expression of Nanog prevents ES cell differentiation even when Klf4 gene expression is knocked down. On the other hand, knockdown of Nanog expression induces differentiation of ES cells that overexpress Klf4. Taken together, these results demonstrate that Klf4 functions upstream of Nanog in ES cell self-renewal and in preventing ES cell differentiation.
机译:转录因子Kruppel样因子4(Klf4)对于体细胞重编程至关重要。此外,Klf4与其他Klf家族蛋白在胚胎干(ES)细胞自我更新中似乎起着多余的作用。但是,如何了解Klf4如何调节ES细胞自我更新和体细胞重编程。在这里我们报告Klf4是ES细胞自我更新和维持多能性所必需的,并且Klf4的表达阻止了ES细胞分化,以抑制白血病抑制因子(LIF)或骨形态发生蛋白4(BMP4)的撤离。此外,Klf4直接与Nanog的启动子区域结合并调节其表达。即使敲低Klf4基因表达,Nanog的表达也能阻止ES细胞分化。另一方面,敲除Nanog表达可诱导过度表达Klf4的ES细胞分化。综上所述,这些结果表明,Klf4在ES细胞自我更新和防止ES细胞分化中在Nanog上游起作用。

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