BMP signalling inhibits premature neural differentiation in the mouse embryo

被引:127
作者
Di-Gregorio, Aida
Sancho, Margarida
Stuckey, Daniel W.
Crompton, Lucy A.
Godwin, Jonathan
Mishina, Yuji
Rodriguez, Tristan A.
机构
[1] Univ London Imperial Coll Sci Technol & Med, Mol Embryol Grp, London W12 0NN, England
[2] Univ London Imperial Coll Sci Technol & Med, Transgen Facil, MRC, Ctr Clin Sci, London W12 0NN, England
[3] NIEHS, Reprod & Dev Toxicol Lab, Mol Dev Biol Sect, Res Triangle Pk, NC 27709 USA
来源
DEVELOPMENT | 2007年 / 134卷 / 18期
基金
英国医学研究理事会;
关键词
neural induction; Bmpr1a; BMP signalling;
D O I
10.1242/dev.005967
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The specification of a subset of epiblast cells to acquire a neural fate constitutes the first step in the generation of the nervous system. Little is known about the signals required for neural induction in the mouse. We have analysed the role of BMP signalling in this process. We demonstrate that prior to gastrulation, Bmp2/4 signalling via Bmpr1a maintains epiblast pluripotency and prevents precocious neural differentiation of this tissue, at least in part by maintaining Nodal signalling. We find that during gastrulation, BMPs of the 60A subgroup cooperate with Bmp2/4 to maintain pluripotency. The inhibition of neural fate by BMPs is independent of FGF signalling, as inhibition of FGF signalling between 5.5 and 7.5 days post-coitum does not block neural differentiation in the mouse embryo. Together, our results demonstrate that inhibition of BMP signalling has a central role during neural induction in mammals and suggest that FGFs do not act as neural inducers in the post-implantation mouse embryo.
引用
收藏
页码:3359 / 3369
页数:11
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