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Contact-dependent promotion of cell migration by the OL-protocadherin–Nap1 interaction

机译:OL-procadcadherin-Nap1相互作用的接触依赖性促进细胞迁移

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摘要

OL-protocadherin (OL-pc) is a transmembrane protein belonging to the cadherin superfamily, which has been shown to accumulate at cell–cell contacts via its homophilic interaction, but its molecular roles remain elusive. In this study, we show that OL-pc bound Nck-associated protein 1 (Nap1), a protein that regulates WAVE-mediated actin assembly. In astrocytoma U251 cells not expressing OL-pc, Nap1 was localized only along the lamellipodia. However, exogenous expression of OL-pc in these cells recruited Nap1 as well as WAVE1 to cell–cell contact sites. Although OL-pc expression had no effect on the motility of solitary U251 cells, it accelerated their movement when they were in contact with one another, causing concomitant reorganization of F-actin and N-cadherin at cell junctions. OL-pc mutants lacking the Nap1-binding site exhibited no such effect. N-cadherin knockdown mimicked OL-pc expression in enhancing cell movement. These results suggest that OL-pc remodels the motility and adhesion machinery at cell junctions by recruiting the Nap1–WAVE1 complex to these sites and, in turn, promotes the migration of cells.
机译:OL-procadadherin(OL-pc)是一种属于钙粘着蛋白超家族的跨膜蛋白,已被证明可通过其亲缘相互作用积聚在细胞间,但其分子作用仍然难以捉摸。在这项研究中,我们显示OL-pc结合Nck相关蛋白1(Nap1),该蛋白调节WAVE介导的肌动蛋白组装。在不表达OL-pc的星形细胞瘤U251细胞中,Nap1仅沿片状脂膜定位。但是,OL-pc在这些细胞中的外源表达招募了Nap1和WAVE1到细胞间的接触部位。尽管OL-pc表达对单独的U251细胞的运动没有影响,但当它们相互接触时,它会加速其运动,从而在细胞连接处伴随F-肌动蛋白和N-钙粘蛋白的重组。缺少Nap1结合位点的OL-pc突变体没有这种作用。 N-钙粘蛋白敲低模仿增强细胞运动的OL-pc表达。这些结果表明,OL-pc通过将Nap1-WAVE1复合物募集到这些位点来重塑细胞连接处的运动性和粘附机制,进而促进细胞的迁移。

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