Troxell M L, Gopalakrishnan S, McCormack J, Poteat B A, Pennington J, Garringer S M, Schneeberger E E, Nelson W J, Marrs J A
Department of Molecular Physiology, Beckman Center B109, Stanford University School of Medicine, Stanford, CA 94305-5426, USA.
J Cell Sci. 2000 Mar;113 ( Pt 6):985-96. doi: 10.1242/jcs.113.6.985.
Previous studies have shown that induction of cadherin-mediated cell-cell adhesion leads to tight junction formation, and that blocking cadherin-mediated cell-cell adhesion inhibits tight junction assembly. Here we report analysis of tight junction assembly in MDCK cells overexpressing a mutant E-cadherin protein that lacks an adhesive extracellular domain (T151 cells). Mutant E-cadherin overexpression caused a dramatic reduction in endogenous cadherin levels. Despite this, tight junction assembly was extensive. The number of tight junction strands observed by freeze-fracture electron microscopy significantly increased in T151 cells compared to that in control cells. Our data indicate that the hierarchical regulation of junctional complex assembly is not absolute, and that inhibition of cadherin function has both positive and negative effects on tight junction assembly.
先前的研究表明,诱导钙黏蛋白介导的细胞-细胞黏附会导致紧密连接的形成,而阻断钙黏蛋白介导的细胞-细胞黏附则会抑制紧密连接的组装。在此,我们报告了对过表达缺乏黏附性细胞外结构域的突变型E-钙黏蛋白的MDCK细胞(T151细胞)中紧密连接组装的分析。突变型E-钙黏蛋白的过表达导致内源性钙黏蛋白水平显著降低。尽管如此,紧密连接的组装仍广泛存在。与对照细胞相比,通过冷冻断裂电子显微镜观察到的T151细胞中紧密连接链的数量显著增加。我们的数据表明,连接复合体组装的分级调控并非绝对,并且钙黏蛋白功能的抑制对紧密连接组装既有正面影响也有负面影响。