Kim Yuna, Bingham Nathan, Sekido Ryohei, Parker Keith L, Lovell-Badge Robin, Capel Blanche
Department of Cell Biology, Duke University Medical Center, Durham, NC 27710, USA.
Proc Natl Acad Sci U S A. 2007 Oct 16;104(42):16558-63. doi: 10.1073/pnas.0702581104. Epub 2007 Oct 10.
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.
在小鼠中对Fgf9进行靶向诱变会导致雄性向雌性的性反转。在四种FGF受体中,FGFR2基于抗体染色显示出两种高度特异性的模式,这表明它可能是性腺中介导FGF9信号传导的受体。在增殖的体腔上皮细胞的质膜和支持细胞祖细胞的细胞核中检测到FGFR2。这种表达模式表明Fgfr2可能在睾丸发育中发挥不止一种作用。为了验证Fgfr2是雄性性别决定所必需的这一假设,我们将携带Fgfr2的floxed等位基因的小鼠与两种不同的Cre品系杂交,以诱导该受体的时间性或细胞特异性缺失。结果表明,胚胎性腺中Fgfr2的缺失模拟了Fgf9的缺失,并导致雄性向雌性的性反转。利用这两种Cre品系,我们提供了首个遗传学证据,证明Fgfr2在睾丸发育过程中的增殖和支持细胞分化中发挥着不同的作用。