Frendo Jean-Louis, Cronier Laurent, Bertin Gwladys, Guibourdenche Jean, Vidaud Michel, Evain-Brion Daniele, Malassine Andre
Institut National de la Santé et de la Recherche Médicale, U427, Paris, France.
J Cell Sci. 2003 Aug 15;116(Pt 16):3413-21. doi: 10.1242/jcs.00648. Epub 2003 Jul 2.
The syncytiotrophoblast is the principal component of the human placenta involved in feto-maternal exchanges and hormone secretion. The syncytiotrophoblast arises from the fusion of villous cytotrophoblasts. We recently showed that functional gap junctional intercellular communication (GJIC) is an important prerequisite for syncytiotrophoblast formation and that connexin 43 (Cx43) is present in cytotrophoblasts and in the syncytiotrophoblast. To determine whether Cx43 is directly involved in trophoblast fusion, we used an antisense strategy in primary cultures of human villous cytotrophoblasts that spontaneously differentiate into the syncytiotrophoblast by cell fusion. We assessed the morphological and functional differentiation of trophoblasts by desmoplakin immunostaining, by quantifying hCG (human chorionic gonadotropin) production and by measuring the expression of specific trophoblast genes (hCG and HERV-W). Furthermore, we used the gap-FRAP (fluorescence recovery after photobleaching) method to investigate functional GJIC. Cytotrophoblasts treated with Cx43 antisense aggregated and fused poorly. Furthermore, less HERV-W env mRNA, hCGbeta mRNA and hCG secretion were detected in Cx43 antisense-treated cytotrophoblasts than in cells treated with scrambled antisense. Treatment with Cx43 antisense dramatically reduced the percentage of coupled trophoblast cells. Taken together, these results suggest that Cx43 is directly involved in human trophoblast cell-cell communication, fusion and differentiation.
合体滋养层是人类胎盘参与母胎物质交换和激素分泌的主要成分。合体滋养层由绒毛细胞滋养层融合形成。我们最近发现,功能性缝隙连接细胞间通讯(GJIC)是合体滋养层形成的重要前提条件,并且连接蛋白43(Cx43)存在于细胞滋养层和合体滋养层中。为了确定Cx43是否直接参与滋养层融合,我们在人绒毛细胞滋养层原代培养物中采用了反义策略,这些细胞通过细胞融合自发分化为合体滋养层。我们通过桥粒斑蛋白免疫染色、定量检测人绒毛膜促性腺激素(hCG)的产生以及测量特定滋养层基因(hCG和HERV-W)的表达来评估滋养层的形态和功能分化。此外,我们使用了间隙荧光漂白恢复(gap-FRAP)方法来研究功能性GJIC。用Cx43反义寡核苷酸处理的细胞滋养层聚集和融合较差。此外,与用乱序反义寡核苷酸处理的细胞相比,在Cx43反义寡核苷酸处理的细胞滋养层中检测到的HERV-W env mRNA、hCGβ mRNA和hCG分泌较少。用Cx43反义寡核苷酸处理显著降低了耦合滋养层细胞的百分比。综上所述,这些结果表明Cx43直接参与人类滋养层细胞间通讯、融合和分化。