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

Yuna Kim, Nathan Bingham, Ryohei Sekido, Keith L. Parker, Robin Lovell-Badge, Blanche Capel*

*Corresponding author for this work

    Research output: Contribution to journalArticlepeer-review

    Abstract

    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.

    Original languageEnglish
    Pages (from-to)16558-16563
    Number of pages6
    JournalProceedings of the National Academy of Sciences of the United States of America
    Volume104
    Issue number42
    DOIs
    Publication statusPublished - 16 Oct 2007

    Keywords

    • Fgfr2
    • growth factor signaling
    • organogenesis
    • sertoli cells
    • testis determination

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