Department of Anatomy and Cell Biology, Carver College of Medicine, University of Iowa, Iowa City, IA 52242, USA.
Mol Biol Cell. 2011 Dec;22(24):4787-800. doi: 10.1091/mbc.E11-07-0657. Epub 2011 Oct 19.
Tight junctions (TJs) are structures indispensable to epithelial cells and are responsible for regulation of paracellular diffusion and maintenance of cellular polarity. Although many interactions between TJ constituents have been identified, questions remain concerning how specific functions of TJs are established and regulated. Here we investigated the roles of Ral GTPases and their common effector exocyst complex in the formation of nascent TJs. Unexpectedly, RNA interference-mediated suppression of RalA or RalB caused opposing changes in TJ development. RalA reduction increased paracellular permeability and decreased incorporation of components into TJs, whereas RalB reduction decreased paracellular permeability and increased incorporation of components into TJs. Activities of both Ral GTPases were mediated through the exocyst. Finally, we show that TJ-mediated separation of apical-basal membrane domains is established prior to equilibration of barrier function and that it is unaffected by Ral knockdown or specific composition of TJs.
紧密连接(TJs)是上皮细胞所必需的结构,负责调节细胞旁扩散和维持细胞极性。尽管已经确定了 TJ 成分之间的许多相互作用,但关于如何建立和调节 TJ 的特定功能仍存在疑问。在这里,我们研究了 Ral GTPases 及其共同效应物外核复合物在新生 TJ 形成中的作用。出乎意料的是,RNA 干扰介导的 RalA 或 RalB 抑制导致 TJ 发育的相反变化。RalA 减少增加了细胞旁通透性并减少了 TJ 成分的掺入,而 RalB 减少则降低了细胞旁通透性并增加了 TJ 成分的掺入。两种 Ral GTPases 的活性均通过外核复合物介导。最后,我们表明,TJ 介导的顶端-基底膜域的分离是在屏障功能达到平衡之前建立的,并且不受 Ral 敲低或 TJ 的特定组成的影响。