Clostridium sordellii lethal toxin (LT) is a glucosyltransferase which inactivates small GTPases from the Rho and Ras families. In the present work, we studied the effects of two variants, LT82 and LT9048, on the integrity of epithelial cell barrier using polarized MCCD (Mouse Cortical Collecting Duct) and MDCK (Madin-Darby Canine Kidney) cells. Our results demonstrate for the first time that LTs have very limited effects on tight junctions. In contrast, we show that both toxins modified the paracellular permeability within 2-4 h. Concomitantly LT82 and LT9048 induced a disorganization of basolateral actin filaments, without modifying apical actin. Both toxins mainly altered adherens junctions by removing E-cadherin-catenin complexes from the membrane to the cytosol. Similar effects on adherens junctions have been observed with other toxins, which directly or indirectly depolymerize actin. Thereby, Rac, a common substrate of both LTs, might play a central role in LT-dependent adherens junction alteration. Here, we show that adherens junction perturbation induced by LTs results neither from a direct effect of toxins on adherens junction proteins nor from an actin-independent Rac pathway, but rather from a Rac-dependent disorganization of basolateral actin cytoskeleton. This further supports that a dynamic equilibrium of cortical actin filaments is essential for functional E-cadherin organization in epithelia.

译文

梭状芽孢杆菌致死毒素 (LT) 是一种葡萄糖基转移酶,可使Rho和Ras家族的小GTPases失活。在目前的工作中,我们使用极化MCCD (小鼠皮质收集管) 和MDCK (Madin-Darby犬肾) 细胞研究了两种变体LT82和LT9048对上皮细胞屏障完整性的影响。我们的结果首次证明了LTs对紧密连接的影响非常有限。相反,我们显示两种毒素在2-4小时内都改变了细胞旁通透性。伴随LT82和LT9048引起基底外侧肌动蛋白丝的混乱,而没有改变顶端肌动蛋白。两种毒素主要通过将E-钙粘蛋白-连环蛋白复合物从膜去除到胞质溶胶来改变粘附连接。其他毒素也观察到对粘附连接的类似作用,这些毒素直接或间接解聚肌动蛋白。因此,Rac是两种LTs的共同底物,可能在依赖LT的粘附结改变中起着核心作用。在这里,我们表明LTs诱导的粘附连接扰动既不是由毒素对粘附连接蛋白的直接作用也不是由肌动蛋白独立的Rac途径引起的,而是由Rac依赖性的基底外侧肌动蛋白细胞骨架的分解引起的。这进一步支持皮质肌动蛋白丝的动态平衡对于上皮细胞中功能性E-钙粘蛋白组织至关重要。

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