E-钙粘素是在胚胎发育中最早表达的分子之一,它可以与Catenin家族成员形成钙粘素/Catenin复合物参与多种细胞功能,对于胚胎植入和胎盘发生具有重要作用.通过RT-PCR、免疫组织化学、细胞粘附分析等方法,在人正常妊娠和输卵管妊娠母胎界面上,发现E-钙粘素主要定位于绒毛细胞滋养层细胞和滋养层细胞柱,从滋养层细胞柱近端向远端,其蛋白质水平逐渐降低.正常胎盘组织中E-钙粘素水平在妊娠早期较高,妊娠中期直至分娩期均维持低水平.在体外培养的人正常胎盘细胞滋养层细胞系(NPC细胞)中,转化生长因子β(TGFβ1)显著上调E-钙粘素蛋白和mRNA的表达,并呈现时间和剂量依赖性,同时,TGFβ1促进NPC细胞之间的粘附.上述结果表明,胎盘中存在E-钙粘素的旁分泌调节机制,E-钙粘素可通过调节滋养层细胞粘附而参与细胞侵润的有节制调控.
E-cadherin was one of the early expressed genes during embryo development. The intact form of E-cadherin can link to cytoskeleton via β catenin, and the complex plays essential roles in cell adhesion. Evidences indicated the essential functions of E-cadherin in processes of embryoic implantation and placentation. Immunohistochemistry and RT-PCR were used to identify the localization of E-cadherin in human placenta. It was found that E-cadherin was expressed mainly in villous cytotrophoblasts and trophoblast column, with the immunoreactivity decreased obviously in distal trophoblast column. Temporally, the mRNA level of E-cadherin in placenta was the highest at gestaional week 6, and began to be down-regulated from week 8 on, reaching a nadir at week 9. However, the mRNA expression was up-regulated in placenta at week 26 and full-term. In human normal placenta origin cytotrophoblast cell line (NPC), the mRNA and protein expressions of E-cadherin was significantly stimulated by TGFβ1 in dose- and time-dependent manners. Meanwhile, the cell-cell adhesion of NPC cells was promoted by TGFβ1. All these data indicated that there exists paracrine regulation of E-cadherin in human placenta, and E-cadherin may be involved in regulating trophoblast cell behaviors, likely inhibiting cell invasion through facilitating cell-cell adhesion.