Erk Signaling Suppresses Embryonic Stem Cell Self-Renewal to Specify Endoderm

被引:86
作者
Hamilton, William B. [1 ]
Brickman, Joshua M. [1 ]
机构
[1] Univ Copenhagen, Danish Stem Cell Ctr DanStem, DK-2200 Copenhagen, Denmark
来源
CELL REPORTS | 2014年 / 9卷 / 06期
关键词
PRIMITIVE ENDODERM; PLURIPOTENTIAL CELLS; PROTEIN-KINASE; GROUND-STATE; G1; PHASE; MOUSE; DIFFERENTIATION; NANOG; FGF; EXPRESSION;
D O I
10.1016/j.celrep.2014.11.032
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Fgf signaling via Erk activation has been associated with both neural induction and the generation of a primed state for the differentiation of embryonic stem cells (ESCs) to all somatic lineages. To dissect the role of Erk in both ESC self-renewal and lineage specification, we explored the requirements for this pathway in various in vitro differentiation settings. A combination of pharmacological inhibition of Erk signaling and genetic loss of function reveal a role for Erk signaling in endodermal, but not neural differentiation. Neural differentiation occurs normally despite a complete block to Erk phosphorylation. In support of this, Erk activation in ESCs derepresses primitive endoderm (PrE) gene expression as a consequence of inhibiting the pluripotent/epiblast network. The early response to Erk activation correlates with functional PrE priming, whereas sustained Erk activity results in PrE differentiation. Taken together, our results suggest that Erk signaling suppresses pluripotent gene expression to enable endodermal differentiation.
引用
收藏
页码:2056 / 2070
页数:15
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