BMP receptor IA is required in the mammalian embryo for endodermal morphogenesis and ectodermal patterning

被引:52
作者
Davis, S
Miura, S
Hill, C
Mishina, Y
Klingensmith, J
机构
[1] Duke Univ, Med Ctr, Dept Cell Biol, Durham, NC 27710 USA
[2] NIEHS, Reprod & Dev Toxicol Lab, Res Triangle Pk, NC 27709 USA
关键词
BMPRIA; BMP signaling; epiblast; mouse; forebrain; ectoderm; endoderm; anterior visceral endoderm;
D O I
10.1016/j.ydbio.2004.01.048
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
BMPRIA is a receptor for bone morphogenetic proteins with high affinity for BMP2 and BMP4. Mouse embryos lacking Bmprla fail to gastrulate, complicating studies on the requirements for BMP signaling in germ layer development. Recent work shows that BMP4 produced in extraembryonic tissues initiates gastrulation. Here we use a conditional allele of Bmprla to remove BMPRIA only in the epiblast, which gives rise to all embryonic tissues. Resulting embryos are mosaics composed primarily of cells homozygous null for Bmprla, interspersed with heterozygous cells. Although mesoderm and endoderm do not form in Bmprla null embryos, these tissues are present in the mosaics and are populated with mutant cells. Thus, BMPRIA signaling in the epiblast does not restrict cells to or from any of the germ layers. Cells lacking Bmprla also contribute to surface ectoderm; however, from the hindbrain forward, little surface ectoderm forms and the forebrain is enlarged and convoluted. Prechordal plate, early definitive endoderm, and anterior visceral endoderm appear to be expanded, likely due to defective morphogenesis. These data suggest that the enlarged forebrain is caused in part by increased exposure of the ectoderm to signaling sources that promote anterior neural fate. Our results reveal critical roles for BMP signaling in endodermal morphogenesis and ectodermal patterning. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:47 / 63
页数:17
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