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Differential caveolin-1 polarization in endothelial cells during migration in two and three dimensions

机译:二维和三维迁移过程中内皮细胞的Caveolin-1差异极化

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Endothelial cell (EC) migration is a critical event during multiple physiological and pathological processes. ECs move in the plane of the endothelium to heal superficially injured blood vessels but migrate in three dimensions during angiogenesis. We herein investigate differences in these modes of movement focusing on caveolae and their defining protein caveolin-1. Using a novel approach for morphological analysis of transmigrating cells, we show that ECs exhibit a polarized distribution of caveolin-1 when traversing a filter pore. Strikingly, in these cells caveolin-1 seems to be released from caveolar structures in the cell rear and to relocalize at the cell front in a cytoplasmic form. In contrast, during planar movement caveolin-1 is concentrated at the rear of ECs, colocalizing with caveolae. The phosphorylatable Tyr(14) residue of caveolin-1 is required for polarization of the protein during transmigration but does not alter polarization during planar movement. Palmitoylation of caveolin-1 is not essential for redistribution of the protein during either mode of movement. Thus, ECs migrating in three dimensions uniquely exhibit dissociation of caveolin-1 from caveolae and phosphorylation-dependent relocalization to the cell front. [References: 52]
机译:内皮细胞(EC)迁移是多种生理和病理过程中的关键事件。 EC在内皮平面内移动以治愈表面受损的血管,但在血管生成过程中会在三个维度上迁移。我们在本文中研究这些运动模式的差异,重点是小窝及其定义蛋白caveolin-1。使用一种新颖的方法对迁移细胞的形态进行分析,我们发现EC穿越滤膜孔时会表现出Caveolin-1的极化分布。令人惊讶的是,在这些细胞中,caveolin-1似乎从细胞后部的小窝结构中释放出来,并以细胞质形式重新定位在细胞前部。相反,在平面运动过程中,小窝蛋白1集中在EC的后部,与小窝共定位。转运过程中蛋白质的极化需要小窝蛋白1的可磷酸化Tyr(14)残基,但在平面运动期间不会改变极化。在两种运动方式中,caveolin-1的棕榈酰化对于蛋白质的重新分配不是必需的。因此,在三个维度上迁移的ECs独特地显示了caveolin-1从caveolae的解离和依赖磷酸化的重新定位到细胞前沿。 [参考:52]

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