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FGF2 维持 NANOG 并改变 BMP4 诱导的人类胚胎干细胞分化的结果。

FGF2 sustains NANOG and switches the outcome of BMP4-induced human embryonic stem cell differentiation.

机构信息

Morgridge Institute for Research, Madison, WI 53715-7365, USA.

出版信息

Cell Stem Cell. 2011 Mar 4;8(3):326-34. doi: 10.1016/j.stem.2011.01.001.

Abstract

Here, we show that as human embryonic stem cells (ESCs) exit the pluripotent state, NANOG can play a key role in determining lineage outcome. It has previously been reported that BMPs induce differentiation of human ESCs into extraembryonic lineages. Here, we find that FGF2, acting through the MEK-ERK pathway, switches BMP4-induced human ESC differentiation outcome to mesendoderm, characterized by the uniform expression of T (brachyury) and other primitive streak markers. We also find that MEK-ERK signaling prolongs NANOG expression during BMP-induced differentiation, that forced NANOG expression results in FGF-independent BMP4 induction of mesendoderm, and that knockdown of NANOG greatly reduces T induction. Together, our results demonstrate that FGF2 signaling switches the outcome of BMP4-induced differentiation of human ESCs by maintaining NANOG levels through the MEK-ERK pathway.

摘要

在这里,我们表明,随着人类胚胎干细胞(ESC)退出多能状态,NANOG 可以在决定谱系结果方面发挥关键作用。先前已有报道称,BMPs 诱导人类 ESC 分化为胚外谱系。在这里,我们发现 FGF2 通过 MEK-ERK 途径作用,将 BMP4 诱导的人类 ESC 分化结果切换为中胚层,其特征是 T(brachyury)和其他原始条纹标记物的均匀表达。我们还发现,MEK-ERK 信号在 BMP 诱导的分化过程中延长了 NANOG 的表达,强制表达 NANOG 导致 FGF 独立的 BMP4 诱导中胚层,并且敲低 NANOG 大大降低了 T 的诱导。总之,我们的结果表明,FGF2 信号通过 MEK-ERK 途径维持 NANOG 水平,从而改变了 BMP4 诱导的人类 ESC 分化的结果。

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