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BMP 诱导 cochlin 表达,促进小鼠胚胎干细胞的自我更新和抑制神经分化。

BMP induces cochlin expression to facilitate self-renewal and suppress neural differentiation of mouse embryonic stem cells.

机构信息

State Key Laboratory of Biomembrane and Membrane Biotechnology, Tsinghua-Peking Center for Life Sciences, School of Life Sciences, Tsinghua University, Beijing 100084, China.

State Key Laboratory of Biomembrane and Membrane Biotechnology, Tsinghua-Peking Center for Life Sciences, School of Life Sciences, Tsinghua University, Beijing 100084, China.

出版信息

J Biol Chem. 2013 Mar 22;288(12):8053-8060. doi: 10.1074/jbc.M112.433995. Epub 2013 Jan 23.

Abstract

BMP4 maintains self-renewal of mouse embryonic stem cells (ESCs) in collaboration with LIF. Here, we report the identification of a novel key BMP target gene, cochlin (Coch) in mouse ESCs. Coch can be significantly up-regulated by BMP4 specifically in ESCs but not in somatic differentiated cells, and this up-regulation is dependent on the BMP signaling mediators Smad1/5 and Smad4. Overexpression of Coch can partially substitute BMP4 to promote self-renewal of mouse ESCs together with LIF, whereas knockdown of Coch impairs self-renewal marker gene expression even in the presence of both BMP4 and LIF. Further studies showed that COCH could mimic BMP4 in repressing neural differentiation of mouse ESCs upon LIF withdrawal and the inhibitory effect of BMP4 on neural differentiation is compromised by Coch knockdown. Taken together, our data suggest that COCH is a part of the downstream target network of BMP signaling and serves as another important effector to fine-tune mouse ESC fates.

摘要

BMP4 与 LIF 共同维持小鼠胚胎干细胞(ESC)的自我更新。在这里,我们报告了在小鼠 ESC 中鉴定出一种新型关键 BMP 靶基因,即 cochlin(Coch)。BMP4 可特异性地上调 Coch 在 ESC 中的表达,但在体细胞分化细胞中则不然,这种上调依赖于 BMP 信号转导介质 Smad1/5 和 Smad4。Coch 的过表达可部分替代 BMP4 与 LIF 一起促进小鼠 ESC 的自我更新,而 Coch 的敲低则即使在存在 BMP4 和 LIF 的情况下,也会损害自我更新标志物基因的表达。进一步的研究表明,COCH 可以在 LIF 撤出时模拟 BMP4 抑制小鼠 ESC 的神经分化,并且 Coch 敲低会削弱 BMP4 对神经分化的抑制作用。总之,我们的数据表明 COCH 是 BMP 信号下游靶标网络的一部分,是精细调控小鼠 ESC 命运的另一个重要效应因子。

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