Robboy Stanley J, Kurita Takeshi, Baskin Laurence, Cunha Gerald R
Department of Pathology, Duke University, Davison Building, Box 3712, Durham, NC 27710, United States.
Department of Cancer Biology and Genetics, The Comprehensive Cancer Center, Ohio State University, 460 W. 12th Avenue, 812 Biomedical Research Tower, Columbus, OH 43210, United States.
Differentiation. 2017 Sep-Oct;97:9-22. doi: 10.1016/j.diff.2017.08.002. Epub 2017 Aug 11.
We present a detailed review of the embryonic and fetal development of the human female reproductive tract utilizing specimens from the 5th through the 22nd gestational week. Hematoxylin and eosin (H&E) as well as immunohistochemical stains were used to study the development of the human uterine tube, endometrium, myometrium, uterine cervix and vagina. Our study revisits and updates the classical reports of Koff (1933) and Bulmer (1957) and presents new data on development of human vaginal epithelium. Koff proposed that the upper 4/5ths of the vagina is derived from Müllerian epithelium and the lower 1/5th derived from urogenital sinus epithelium, while Bulmer proposed that vaginal epithelium derives solely from urogenital sinus epithelium. These conclusions were based entirely upon H&E stained sections. A central player in human vaginal epithelial development is the solid vaginal plate, which arises from the uterovaginal canal (fused Müllerian ducts) cranially and squamous epithelium of urogenital sinus caudally. Since Müllerian and urogenital sinus epithelium cannot be unequivocally identified in H&E stained sections, we used immunostaining for PAX2 (reactive with Müllerian epithelium) and FOXA1 (reactive with urogenital sinus epithelium). By this technique, the PAX2/FOXA1 boundary was located at the extreme caudal aspect of the vaginal plate at 12 weeks. During the ensuing weeks, the PAX2/FOXA1 boundary progressively extended cranially such that by 21 weeks the entire vaginal epithelium was FOXA1-reactive and PAX2-negative. This observation supports Bulmer's proposal that human vaginal epithelium derives solely from urogenital sinus epithelium. Clearly, the development of the human vagina is far more complex than previously envisioned and appears to be distinctly different in many respects from mouse vaginal development.
我们利用妊娠第5周至第22周的标本,对人类女性生殖道的胚胎和胎儿发育进行了详细综述。采用苏木精和伊红(H&E)染色以及免疫组织化学染色来研究人类输卵管、子宫内膜、子宫肌层、子宫颈和阴道的发育。我们的研究重新审视并更新了科夫(1933年)和布尔默(1957年)的经典报告,并提供了关于人类阴道上皮发育的新数据。科夫提出阴道上五分之四源自苗勒上皮,下五分之一源自泌尿生殖窦上皮,而布尔默则提出阴道上皮仅源自泌尿生殖窦上皮。这些结论完全基于H&E染色切片。人类阴道上皮发育的一个关键因素是实体阴道板,它由头侧的子宫阴道管(融合的苗勒管)和尾侧的泌尿生殖窦鳞状上皮形成。由于在H&E染色切片中无法明确区分苗勒上皮和泌尿生殖窦上皮,我们使用了针对PAX2(与苗勒上皮反应)和FOXA1(与泌尿生殖窦上皮反应)的免疫染色。通过这种技术,在12周时PAX2/FOXA1边界位于阴道板的最尾端。在随后的几周里,PAX2/FOXA1边界逐渐向头侧延伸,以至于到21周时整个阴道上皮对FOXA1呈反应性且PAX2呈阴性。这一观察结果支持了布尔默的提议,即人类阴道上皮仅源自泌尿生殖窦上皮。显然,人类阴道的发育远比之前设想的复杂,并且在许多方面似乎与小鼠阴道发育明显不同。