Eomesodermin induces Mesp1 expression and cardiac differentiation from embryonic stem cells in the absence of Activin

被引:49
|
作者
van den Ameele, Jelle [1 ,2 ]
Tiberi, Luca [1 ]
Bondue, Antoine [1 ,3 ]
Paulissen, Catherine [1 ]
Herpoel, Adele [1 ]
Iacovino, Michelina [4 ]
Kyba, Michael [4 ]
Blanpain, Cedric [1 ,5 ]
Vanderhaeghen, Pierre [1 ,5 ]
机构
[1] Univ Libre Bruxelles, IRIBHM Inst Interdisciplinary Res, B-1070 Brussels, Belgium
[2] Ghent Univ Hosp, Dept Neurol, B-9000 Ghent, Belgium
[3] Erasme Univ Hosp, Dept Cardiol, B-1070 Brussels, Belgium
[4] Univ Texas SW Med Ctr Dallas, Dallas, TX 75390 USA
[5] Univ Libre Bruxelles, WELBIO, IRIBHM, B-1070 Brussels, Belgium
基金
欧洲研究理事会;
关键词
Eomesodermin; Mesp1; Nodal/Activin; cardiac fate; embryonic stem cell; CARDIOVASCULAR PROGENITOR SPECIFICATION; EARLY MOUSE EMBRYO; DEFINITIVE ENDODERM; SMOOTH-MUSCLE; MESODERM FORMATION; PRIMITIVE STREAK; INDUCTION; GASTRULATION; COMMITMENT; ACTIVATION;
D O I
10.1038/embor.2012.23
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The transcription factor Eomesodermin (Eomes) is involved in early embryonic patterning, but the range of cell fates that it controls as well as its mechanisms of action remain unclear. Here we show that transient expression of Eomes promotes cardiovascular fate during embryonic stem cell differentiation. Eomes also rapidly induces the expression of Mesp1, a key regulator of cardiovascular differentiation, and directly binds to regulatory sequences of Mesp1. Eomes effects are strikingly modulated by Activin signalling: high levels of Activin inhibit the promotion of cardiac mesoderm by Eomes, while they enhance Eomes-dependent endodermal specification. These results place Eomes upstream of the Mesp1-dependent programme of cardiogenesis, and at the intersection of mesodermal and endodermal specification, depending on the levels of Activin/Nodal signalling.
引用
收藏
页码:355 / 362
页数:8
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