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Cdc42 的定位和细胞极性依赖于膜转运。

Cdc42 localization and cell polarity depend on membrane traffic.

机构信息

Cell Polarity and Migration Group, Institut Pasteur, and Centre National de la Recherche Scientifique URA 2582, 75724 Paris, Cedex 15, France.

出版信息

J Cell Biol. 2010 Dec 27;191(7):1261-9. doi: 10.1083/jcb.201003091. Epub 2010 Dec 20.

Abstract

Cell polarity is essential for cell division, cell differentiation, and most differentiated cell functions including cell migration. The small G protein Cdc42 controls cell polarity in a wide variety of cellular contexts. Although restricted localization of active Cdc42 seems to be important for its distinct functions, mechanisms responsible for the concentration of active Cdc42 at precise cortical sites are not fully understood. In this study, we show that during directed cell migration, Cdc42 accumulation at the cell leading edge relies on membrane traffic. Cdc42 and its exchange factor βPIX localize to intracytosplasmic vesicles. Inhibition of Arf6-dependent membrane trafficking alters the dynamics of Cdc42-positive vesicles and abolishes the polarized recruitment of Cdc42 and βPIX to the leading edge. Furthermore, we show that Arf6-dependent membrane dynamics is also required for polarized recruitment of Rac and the Par6-aPKC polarity complex and for cell polarization. Our results demonstrate influence of membrane dynamics on the localization and activation of Cdc42 and consequently on directed cell migration.

摘要

细胞极性对于细胞分裂、细胞分化以及大多数分化细胞功能(包括细胞迁移)至关重要。小 G 蛋白 Cdc42 在广泛的细胞环境中控制细胞极性。尽管活性 Cdc42 的受限定位似乎对其独特功能很重要,但负责将活性 Cdc42 集中在精确皮质部位的机制尚未完全了解。在这项研究中,我们表明,在定向细胞迁移过程中,细胞前缘的 Cdc42 积累依赖于膜运输。Cdc42 和其交换因子βPIX 定位于细胞内的小泡。抑制 Arf6 依赖性膜运输会改变 Cdc42 阳性小泡的动态,并消除 Cdc42 和βPIX 向前缘的极化募集。此外,我们还表明,Arf6 依赖性膜动力学对于 Rac 和 Par6-aPKC 极性复合物的极化募集以及细胞极化也是必需的。我们的研究结果表明,膜动力学对 Cdc42 的定位和激活有影响,从而影响定向细胞迁移。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2af2/3010071/72b8c3aee9de/JCB_201003091_RGB_Fig1.jpg

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