Japanese society of Ova Research

Abstract

Vol.31 No.1

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Original
Regulation of Preimplantation Embryo Development in Mice by FMS-like Tyrosine Kinase 3 Ligand
JMOR, 31(1) 45-51, 2014
DOI: 10.1274/jmor.31.45
1Department of Obstetrics and Gynecology, St. Marianna University School of Medicine, Kanagawa 216-8511, Japan
2Department of Advanced Reproductive Medicine, St. Marianna University School of Medicine, Kanagawa 216-8511, Japan
3Department of Obstetrics and Gynecology, Akita University Graduate School of Medicine, Akita 010-8543, Japan
4Department of Dermatology and Plastic Surgery, Akita University Graduate School of Medicine, Akita 010-8543, Japan

Successful development of preimplantation embryos is essential for reproduction. Growth factors secreted by reproductive tracts are important for the development of preimplantation embryos. FMS-like tyrosine kinase 3 (FLT3) is a tyrosine kinase receptor related to colony-stimulating factor-1 receptor and c-KIT, promoting preimplantation embryo development following their ligand binding. We found expression of FLT3 ligand transcripts in the oviducts and uteri of pregnant mice. The transcripts for its receptor, FLT3, were detectable throughout the early embryonic stages with an increase after the eight-cell stage. In contrast, the expression of FLT3 ligand was negligible after the morula stage, suggesting potential paracrine actions of FLT3 ligand produced by the reproductive tracts. Treatment with FLT3 ligand promoted the development of two-cell embryos to the morula and blastocyst stages in a dose-dependent manner with increases in cell proliferation, but not inhibition of cell survival. The effects of FLT3 ligand were blocked by a FLT3 receptor inhibitor, TCS359. Studies using specific inhibitors demonstrated the potential involvement of the PI3K pathway in mediating FLT3 ligand actions. Our findings suggest that the FLT3 ligand/FLT3 signaling system plays important paracrine roles during the development of preimplantation embryos.

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