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

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 th...

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Bibliographic Details
Published in:Developmental biology Vol. 397; no. 1; pp. 45 - 55
Main Authors: Reyes de Mochel, Nabora Soledad, Luong, Mui, Chiang, Michael, Javier, Anna L., Luu, Elizabeth, Toshihiko, Fujimori, MacGregor, Grant R., Cinquin, Olivier, Cho, Ken W.Y.
Format: Journal Article
Language:English
Published: United States Elsevier Inc 01-01-2015
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Summary: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. [Display omitted] •Control of cell division during mouse preimplantation development is poorly defined.•BMP signaling is active during mouse preimplantation development.•BMP signaling is required for cell cleavage in the preimplantation mouse embryo.
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ISSN:0012-1606
1095-564X
DOI:10.1016/j.ydbio.2014.10.001