Kibschull M, Gellhaus A, Winterhager E
Samuel Lunenfeld Research Institute, Mount Sinai Hospital, 600 University Avenue, Toronto, Canada.
Placenta. 2008 Oct;29(10):848-54. doi: 10.1016/j.placenta.2008.07.013. Epub 2008 Sep 9.
Here, we review the expression, localization and the possible role of the different connexin isoforms in placental function and development in mice and men. Connexin gene deletion in mice has shown that Cx26 is responsible for transplacental uptake of glucose in the labyrinth, and Cx31 as well as Cx31.1 for trophoblast cell lineage development. In the human placenta, it appears that Cx43 is required for the fusion process of cytotrophoblastic cells leading to the formation of the syncytiotrophoblast. Thus Cx26 and Cx43 serve different species-specific functions in the functionally analogous placental compartments, mouse labyrinth and human villous trophoblast. However, like Cx31 in the mouse, Cx40 plays a critical role in the switch from a proliferative to an invasive phenotype of the trophoblast cells invading the endometrium. Both connexin channels seem to have similar functions in analogous compartments of the placentas. Taken together, connexins are important in regulating trophoblast cell differentiation in both species. In mouse, connexin channels are specifically involved in passive transport of molecules across the placental barriers.
在此,我们综述了不同连接蛋白亚型在小鼠和人类胎盘功能及发育中的表达、定位和可能作用。小鼠连接蛋白基因缺失研究表明,Cx26负责胎盘迷路中葡萄糖的跨胎盘摄取,Cx31以及Cx31.1则参与滋养层细胞谱系发育。在人类胎盘中,细胞滋养层细胞融合形成合体滋养层似乎需要Cx43。因此,Cx26和Cx43在功能类似的胎盘结构(小鼠迷路和人类绒毛滋养层)中发挥不同的物种特异性功能。然而,与小鼠中的Cx31一样,Cx40在侵入子宫内膜的滋养层细胞从增殖表型向侵袭表型转变中起关键作用。这两种连接蛋白通道在胎盘的类似结构中似乎具有相似功能。总之,连接蛋白在调节这两个物种的滋养层细胞分化中都很重要。在小鼠中,连接蛋白通道专门参与分子跨胎盘屏障的被动转运。