Brüser Lena, Bogdan Sven
Institut für Neurobiologie, Universität Münster, Badestraße 9, 48149 Münster, Germany.
Institut für Physiologie und Pathophysiologie, Abteilung Molekulare Zellphysiologie, Phillips-Universität Marburg, Emil-Mannkopff-Straße 2, 35037 Marburg, Germany.
Cold Spring Harb Perspect Biol. 2017 Mar 1;9(3):a029140. doi: 10.1101/cshperspect.a029140.
Cadherin-based adherens junctions are conserved structures that mediate epithelial cell-cell adhesion in invertebrates and vertebrates. Despite their pivotal function in epithelial integrity, adherens junctions show a remarkable plasticity that is a prerequisite for tissue architecture and morphogenesis. Epithelial cadherin (E-cadherin) is continuously turned over and undergoes cycles of endocytosis, sorting and recycling back to the plasma membrane. Mammalian cell culture and genetically tractable model systems such as have revealed conserved, but also distinct, mechanisms in the regulation of E-cadherin membrane trafficking. Here, we discuss our current knowledge about molecules and mechanisms controlling endocytosis, sorting and recycling of E-cadherin during junctional remodeling.
基于钙黏蛋白的黏附连接是保守结构,介导无脊椎动物和脊椎动物上皮细胞间的黏附。尽管黏附连接在上皮完整性中起关键作用,但它们表现出显著的可塑性,这是组织结构和形态发生的先决条件。上皮钙黏蛋白(E-钙黏蛋白)不断更新,经历内吞、分选和再循环回到质膜的循环过程。哺乳动物细胞培养以及诸如(此处原文缺失相关内容)等易于进行基因操作的模型系统揭示了E-钙黏蛋白膜运输调控中保守但也有区别的机制。在此,我们讨论关于在连接重塑过程中控制E-钙黏蛋白内吞、分选和再循环的分子和机制的当前知识。