Fibroblast growth factor receptor 2 regulates proliferation and Sertoli differentiation during male sex determination

被引:129
|
作者
Kim, Yuna
Bingham, Nathan
Sekido, Ryohei
Parker, Keith L.
Lovell-Badge, Robin
Capel, Blanche
机构
[1] Duke Univ, Ctr Med, Dept Cell Biol, Durham, NC 27710 USA
[2] Univ Texas, SW Med Ctr, Dept Internal Med, Dallas, TX 75390 USA
[3] Natl Inst Med Res, MRC, Div Dev Genet, London NW7 1AA, England
基金
英国医学研究理事会;
关键词
Fgfr2; growth factor signaling; organcogenesis; Sertoli cells; testis determination;
D O I
10.1073/pnas.0702581104
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Targeted mutagenesis of Fgf9 in mice causes male-to-female sex reversal. Among the four FGF receptors, FGFR2 showed two highly specific patterns based on antibody staining, suggesting that it might be the receptor-mediating FGF9 signaling in the gonad. FGFR2 was detected at the plasma membrane in proliferating coelomic epithelial cells and in the nucleus in Sertoli progenitor cells. This expression pattern suggested that Fgfr2 might play more than one role in testis development. To test the hypothesis that Fgfr2 is required for male sex determination, we crossed mice carrying a floxed allele of Fgfr2 with two different Cre lines to induce a temporal or cell-specific deletion of this receptor. Results show that deletion of Fgfr2 in embryonic gonads phenocopies deletion of Fgf9 and leads to male-to-female sex reversal. Using these two Cre lines, we provide the first genetic evidence that Fgfr2 plays distinct roles in proliferation and Sertoli cell differentiation during testis development.
引用
收藏
页码:16558 / 16563
页数:6
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