FGF2 Sustains NANOG and Switches the Outcome of BMP4-Induced Human Embryonic Stem Cell Differentiation

被引:197
|
作者
Yu, Pengzhi [1 ,2 ,3 ]
Pan, Guangjin [1 ]
Yu, Junying [4 ]
Thomson, James A. [1 ,2 ,5 ]
机构
[1] Morgridge Inst Res, Madison, WI 53715 USA
[2] Univ Wisconsin, Sch Med & Publ Hlth, Madison, WI 53707 USA
[3] Univ Wisconsin, Grad Program Cellular & Mol Biol, Madison, WI 53706 USA
[4] Cellular Dynam Int Inc, Madison, WI 53707 USA
[5] Univ Calif Santa Barbara, Dept Mol Cellular & Dev Biol, Santa Barbara, CA 93106 USA
关键词
BONE MORPHOGENETIC PROTEIN-4; HUMAN ES CELLS; MOUSE EPIBLAST; MESODERM INDUCTION; BRACHYURY T; DUSP6; MKP3; PLURIPOTENCY; EXPRESSION; CLONING; FAMILY;
D O I
10.1016/j.stem.2011.01.001
中图分类号
Q813 [细胞工程];
学科分类号
摘要
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.
引用
收藏
页码:326 / 334
页数:9
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