Bear J E, Loureiro J J, Libova I, Fässler R, Wehland J, Gertler F B
Department of Biology, Massachusetts Institute of Technology, Cambridge, USA.
Cell. 2000 Jun 23;101(7):717-28. doi: 10.1016/s0092-8674(00)80884-3.
Ena/VASP proteins have been implicated in cell motility through regulation of the actin cytoskeleton and are found at focal adhesions and the leading edge. Using overexpression, loss-of-function, and inhibitory approaches, we find that Ena/VASP proteins negatively regulate fibroblast motility. A dose-dependent decrease in movement is observed when Ena/VASP proteins are overexpressed in fibroblasts. Neutralization or deletion of all Ena/VASP proteins results in increased cell movement. Selective depletion of Ena/VASP proteins from focal adhesions, but not the leading edge, has no effect on motility. Constitutive membrane targeting of Ena/VASP proteins inhibits motility. These results are in marked contrast to current models for Ena/VASP function derived mainly from their role in the actin-driven movement of Listeria monocytogenes.
Ena/VASP蛋白通过调节肌动蛋白细胞骨架参与细胞运动,并存在于粘着斑和前沿。通过过表达、功能缺失和抑制方法,我们发现Ena/VASP蛋白对成纤维细胞运动起负调节作用。当在成纤维细胞中过表达Ena/VASP蛋白时,观察到运动呈剂量依赖性下降。中和或缺失所有Ena/VASP蛋白会导致细胞运动增加。从粘着斑而非前沿选择性耗尽Ena/VASP蛋白对运动没有影响。Ena/VASP蛋白的组成型膜靶向抑制运动。这些结果与目前主要基于Ena/VASP蛋白在单核细胞增生李斯特菌肌动蛋白驱动运动中的作用得出的Ena/VASP功能模型形成鲜明对比。