Department of Medicine, University of Rochester, Rochester, NY 14642, USA.
Mol Biol Cell. 2010 Oct 15;21(20):3506-17. doi: 10.1091/mbc.E10-03-0259. Epub 2010 Sep 1.
Epithelial adherens junctions (AJs) and tight junctions (TJs) are dynamic structures that readily undergo disintegration and reassembly. Remodeling of the AJs and TJs depends on the orchestrated dynamics of the plasma membrane with its underlying F-actin cytoskeleton, and the membrane-cytoskeleton interface may play a key role in junctional regulation. Spectrin-adducin-ankyrin complexes link membranes to the actin cytoskeleton where adducins mediate specrtrin-actin interactions. This study elucidates roles of adducins in the remodeling of epithelial junctions in human SK-CO15 colonic and HPAF-II pancreatic epithelial cell monolayers. These cells expressed the α and γ isoforms of adducin that positively regulated each others protein level and colocalized with E-cadherin and β-catenin at mature, internalized and newly assembled AJs. Small interfering RNA-mediated down-regulation of α- or γ-adducin expression significantly attenuated calcium-dependent AJ and TJ assembly and accelerated junctional disassembly triggered by activation of protein kinase C. Two mechanisms were found to mediate the impaired AJ and TJ assembly in adducin-depleted cells. One mechanism involved diminished expression and junctional recruitment of βII-spectrin, and the other mechanism involved the decrease in the amount of cellular F-actin and impaired assembly of perijunctional actin bundles. These findings suggest novel roles for adducins in stabilization of epithelial junctions and regulation of junctional remodeling.
上皮细胞黏附连接(AJs)和紧密连接(TJs)是易于发生解体和重组的动态结构。AJs 和 TJs 的重塑取决于质膜及其下的 F-肌动蛋白细胞骨架的协调动力学,而膜-细胞骨架界面可能在连接调节中发挥关键作用。血影蛋白-连接蛋白-锚蛋白复合物将膜与肌动蛋白细胞骨架连接起来,其中连接蛋白介导血影蛋白与肌动蛋白的相互作用。本研究阐明了连接蛋白在人 SK-CO15 结肠和 HPAF-II 胰腺上皮细胞单层上皮连接重塑中的作用。这些细胞表达了连接蛋白的α和γ同工型,它们正向调节彼此的蛋白水平,并与 E-钙黏蛋白和β-连环蛋白在成熟的、内化的和新组装的 AJs 中共定位。通过小干扰 RNA 介导的α或γ连接蛋白表达下调,显著减弱了钙依赖性 AJ 和 TJ 的组装,并加速了蛋白激酶 C 激活触发的连接解体。发现两种机制介导了连接蛋白耗尽细胞中 AJ 和 TJ 组装受损。一种机制涉及βII-血影蛋白表达和连接募集的减少,另一种机制涉及细胞 F-肌动蛋白的减少和周缘肌动蛋白束组装受损。这些发现表明连接蛋白在稳定上皮连接和调节连接重塑方面具有新的作用。