Fukunaga Yoshitaka, Liu Huijie, Shimizu Masayuki, Komiya Satoshi, Kawasuji Michio, Nagafuchi Akira
Division of Cellular Interactions, Institute of Molecular Embryology and Genetics, Kumamoto University, Honjo 2-2-1, Kumamoto 860-0811, Japan.
Cell Struct Funct. 2005;30(2):25-34. doi: 10.1247/csf.30.25.
F9 teratocarcinoma cells in which beta-catenin and/or plakoglobin genes are knocked-out were generated and investigated in an effort to define the role of beta-catenin and plakoglobin in cell adhesion. Loss of beta-catenin expression only did not affect cadherin-mediated cell adhesion activity. Loss of both beta-catenin and plakoglobin expression, however, severely affected the strong cell adhesion activity of cadherin. In beta-catenin-deficient cells, the amount of plakoglobin associated with E-cadherin dramatically increased. In beta-catenin/plakoglobin-deficient cells, the level of E-cadherin and alpha-catenin markedly decreased. In these cells, E-cadherin formed large aggregates in cytoplasm and membrane localization of alpha-catenin was barely detected. These data confirmed that beta-catenin or plakoglobin is required for alpha-catenin to form complex with E-cadherin. It was also demonstrated that plakoglobin can compensate for the absence of beta-catenin. Moreover it was suggested that beta-catenin or plakoglobin is required not only for the cell adhesion activity but also for the stable expression and cell surface localization of E-cadherin.
为了确定β-连环蛋白和桥粒斑珠蛋白在细胞黏附中的作用,我们构建并研究了β-连环蛋白和/或桥粒斑珠蛋白基因敲除的F9畸胎瘤细胞。仅β-连环蛋白表达缺失并不影响钙黏蛋白介导的细胞黏附活性。然而,β-连环蛋白和桥粒斑珠蛋白表达均缺失则严重影响钙黏蛋白的强细胞黏附活性。在β-连环蛋白缺陷细胞中,与E-钙黏蛋白相关的桥粒斑珠蛋白量显著增加。在β-连环蛋白/桥粒斑珠蛋白缺陷细胞中,E-钙黏蛋白和α-连环蛋白水平明显降低。在这些细胞中,E-钙黏蛋白在细胞质中形成大聚集体,几乎检测不到α-连环蛋白的膜定位。这些数据证实,β-连环蛋白或桥粒斑珠蛋白是α-连环蛋白与E-钙黏蛋白形成复合物所必需的。还证明桥粒斑珠蛋白可以补偿β-连环蛋白的缺失。此外,提示β-连环蛋白或桥粒斑珠蛋白不仅是细胞黏附活性所必需的,也是E-钙黏蛋白稳定表达和细胞表面定位所必需的。