BMP signaling is required for cell cleavage in preimplantation-mouse embryos

被引:31
作者
de Mochel, Nabora Soledad Reyes [1 ]
Luong, Mui [1 ]
Chiang, Michael [1 ]
Javier, Anna L. [1 ]
Luu, Elizabeth [1 ]
Fujimori, Toshihiko [2 ]
MacGregor, Grant R. [1 ]
Cinquin, Olivier [1 ]
Cho, Ken W. Y. [1 ]
机构
[1] Univ Calif Irvine, Dept Dev & Cell Biol, Irvine, CA 92697 USA
[2] Natl Inst Basic Biol, Div Embryol, Okazaki, Japan
基金
美国国家卫生研究院;
关键词
BMP; Smad1; Morula; Preimplantation; Cell cleavage; Cell division; LOOP-HELIX PROTEINS; TGF-BETA; MUTANT MICE; ID GENES; TROPHECTODERM; BLASTOCYST; DIFFERENTIATION; FAMILY; AXIS; TRANSCRIPTION;
D O I
10.1016/j.ydbio.2014.10.001
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The mechanisms regulating cell division during development of the mouse pre-implantation embryo are poorly understood. We have investigated whether bone morphogenetic protein (BMP) signaling is involved in controlling cell cycle during mouse pre-implantation development. We mapped and quantitated the dynamic activities of BMP signaling through high-resolution immunofluorescence imaging combined with a 3D segmentation method. Immunostaining for phosphorylated Smad1/5/8 shows that BMP signaling is activated in mouse embryos as early as the 4-cell stage, and becomes spatially restricted by late blastocyst stage. Perturbation of BMP signaling in preimplantation mouse embryos, whether by treatment with a small molecule inhibitor, with Noggin protein, or by overexpression of a dominant-negative BMP receptor, indicates that BMPs regulate cell cleavage up to the morula stage. These results indicate that BMP signaling is active during mouse pre-implantation development and is required for cell cleavage in preimplantation mouse embryos. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:45 / 55
页数:11
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