The process of fetal external genitalia development might be divided into two processes. The first process accomplishes the initial outgrowth of the anlage, genital tubercle (GT). Previous analysis suggests that the distal urethral epithelium (DUE) of the GT, the Fgf8-expressing region, regulates the outgrowth of the GT. The second process eventually generates the sexually dimorphic development of the external genitalia, which is dependent on the action of steroid hormones. Several key genes, for example, RARs, RXRs, RALDH2, and CYP26, were dynamically expressed during GT development. The teratogenic dose of RA at 9.0 d.p.c. induced a drastic malformation of the urethral plate during GT formation, but did not show gross abnormalities in its outgrowth. In RA-treated embryos, Fgf8 expression was still detected in the distal GT regions. Possible regulatory roles of the FGF and RA signaling systems in external genitalia formation are discussed.

译文

胎儿外生殖器发育的过程可以分为两个过程。第一个过程完成了肛门生殖器结节(GT)的初始生长。先前的分析表明,GT的远端尿道上皮(DUE)(表达Fgf8的区域)调节了GT的生长。第二个过程最终产生外部生殖器的性二形发育,这取决于类固醇激素的作用。 GT开发过程中动态表达了几个关键基因,例如RAR,RXR,RALDH2和CYP26。 RA的致畸剂量为9.0d.p.c。在GT形成过程中引起尿道板的严重畸形,但未显示出明显的异常生长。在RA治疗的胚胎中,在远端GT区域仍检测到Fgf8表达。讨论了FGF和RA信号系统在外生殖器形成中的可能调控作用。

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