Wartenberg H
Anat Embryol (Berl). 1985;171(3):311-23. doi: 10.1007/BF00347020.
The regression of the male Müllerian duct has been studied in human embryos and fetuses by means of the semi-thin light microscopic technique and by electron microscopy. After completion of the duct's differentiation during week 7, a periductal stroma is formed by two types of mesenchymal-like cells: light, epitheloid cells originating from the coelomic epithelium and dark, fusiform cells of mesonephric origin. During week 9 these cells condense to a compact cuff in which the light cells occupy the inner core. The duct is entirely sealed by an epitheloid stratum of the periductal stroma. At the same time, the basal lamina thickens up to 300 nm by apposition of extracellular material. During weeks 10 to 12, the inner stromal core is invaded by dark fusiform cells from the peripheral stratum which intermingle with the light cells. The basal lamina dissolves, the epithelio-stromal interface becomes indistinct and finally disappears. During week 13 remnants of the Müllerian duct can be observed. They result from the complete merging of the ductal into the periductal compartment. Müllerian duct regression is divided into two functional steps: First the duct is prevented from growth by the epitheloid cells of the stromal cuff. This process lasts for 2 to 3 weeks. In the second place the basal lamina breaks up under the influence of the dark stromal component. This event launches the regression proper and lasts for another 2 to 3 weeks. Necrosis of cells or programmed cell death does not play a decisive role in the regression of the human Müllerian duct. In the upper, nonregressing part of the duct, light epitheloid cells are scarce and do not seal the duct. A periductal extracellular space is preserved during the entire period and the periductal stroma does not fuse with the duct's epithelium. The epithelio-stromal interface is maintained along this section.
利用半薄光学显微镜技术和电子显微镜,对人类胚胎和胎儿中男性苗勒管的退化进行了研究。在第7周导管分化完成后,导管周围基质由两种间充质样细胞形成:起源于体腔上皮的浅色上皮样细胞和中肾起源的深色梭形细胞。在第9周,这些细胞凝聚成一个紧密的套环,其中浅色细胞占据内核。导管完全被导管周围基质的上皮样层封闭。同时,通过细胞外物质的附着,基膜增厚至300纳米。在第10至12周期间,外周层的深色梭形细胞侵入内部基质核心,与浅色细胞混合。基膜溶解,上皮-基质界面变得模糊,最终消失。在第13周,可以观察到苗勒管的残余物。它们是由于导管完全融入导管周围腔室而形成的。苗勒管退化分为两个功能步骤:首先,导管周围套环的上皮样细胞阻止导管生长。这个过程持续2至3周。其次,在深色基质成分的影响下,基膜破裂。这一事件引发了真正的退化,并持续另外2至3周。细胞坏死或程序性细胞死亡在人类苗勒管的退化中不发挥决定性作用。在导管的上部、未退化部分,浅色上皮样细胞稀少,不能封闭导管。在整个时期内,导管周围细胞外间隙得以保留,导管周围基质不与导管上皮融合。沿着这一部分,上皮-基质界面得以维持。