Hashimoto Ryozo
Congenital Anomaly Research Center, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Anat Rec A Discov Mol Cell Evol Biol. 2003 Jun;272(2):514-9. doi: 10.1002/ar.a.10061.
An embryological explanation for the development of the Müllerian duct still poses a major challenge. The development of this duct was investigated systematically in human embryos. Seven embryos (Carnegie stages 18-23) were serially sectioned in the frontal, sagittal, and transversal planes at a thickness of 10 microm and stained with hematoxylin and eosin (H&E) for histological analysis. In all observed embryos, the caudal end of the Müllerian duct was found to be intimately connected to the Wolffian duct. The opening of the Müllerian duct to the coelomic cavity was formed as the result of an invagination of the coelomic epithelium at Carnegie stage 18. The duct grew independently from the invagination during stages 19-23. The fused duct (uterovaginal canal) bifurcated at the caudal portion at Carnegie stages 22 and 23. This is the first description of the caudal portion of the fused Müllerian ducts separating again and returning to each of the Wolffian ducts in human embryos.
苗勒管发育的胚胎学解释仍然是一个重大挑战。对人类胚胎中该管道的发育进行了系统研究。选取了7个胚胎(卡内基分期18 - 23期),分别在额面、矢状面和横断面进行连续切片,切片厚度为10微米,并用苏木精和伊红(H&E)染色以进行组织学分析。在所有观察到的胚胎中,发现苗勒管的尾端与中肾管紧密相连。苗勒管向体腔的开口是在卡内基分期18期时体腔上皮内陷形成的。在19 - 23期,管道从内陷处开始独立生长。融合管道(子宫阴道管)在卡内基分期22和23期时在尾部分叉。这是首次对人类胚胎中融合的苗勒管尾端再次分开并回归到各自中肾管的描述。