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细胞表面动力学——Rho GTPases 如何协调质膜与皮质细胞骨架之间的相互作用。

Cell surface dynamics - how Rho GTPases orchestrate the interplay between the plasma membrane and the cortical cytoskeleton.

机构信息

Vita-Salute San Raffaele University and San Raffaele Scientific Institute, via Olgettina 58, 20132 Milan, Italy.

出版信息

J Cell Sci. 2012 Oct 1;125(Pt 19):4435-44. doi: 10.1242/jcs.108266. Epub 2012 Oct 23.

Abstract

Small GTPases are known to regulate hundreds of cell functions. In particular, Rho family GTPases are master regulators of the cytoskeleton. By regulating actin nucleation complexes, Rho GTPases control changes in cell shape, including the extension and/or retraction of surface protrusions and invaginations. Protrusion and invagination of the plasma membrane also involves the interaction between the plasma membrane and the cortical cytoskeleton. This interplay between membranes and the cytoskeleton can lead to an increase or decrease in the plasma membrane surface area and its tension as a result of the fusion (exocytosis) or internalization (endocytosis) of membranous compartments, respectively. For a long time, the cytoskeleton and plasma membrane dynamics were investigated separately. However, studies from many laboratories have now revealed that Rho GTPases, their modulation of the cytoskeleton, and membrane traffic are closely connected during the dynamic remodeling of the cell surface. Arf- and Rab-dependent exocytosis of specific vesicles contributes to the targeting of Rho GTPases and their regulatory factors to discrete sites of the plasma membrane. Rho GTPases regulate the tethering of exocytic vesicles and modulate their subsequent fusion. They also have crucial roles in the different forms of endocytosis, where they participate in the sorting of membrane domains as well as the sculpting and sealing of membrane flasks and cups. Here, we discuss how cell surface dynamics depend on the orchestration of the cytoskeleton and the plasma membrane by Rho GTPases.

摘要

小分子 GTPases 已知能调节数百种细胞功能。特别是,Rho 家族 GTPases 是细胞骨架的主要调节因子。通过调节肌动蛋白成核复合物,Rho GTPases 控制细胞形状的变化,包括表面突起和凹陷的延伸和/或缩回。质膜的突起和凹陷也涉及质膜与皮质细胞骨架之间的相互作用。膜和细胞骨架之间的这种相互作用可以导致质膜表面积及其张力的增加或减少,这是由于膜性隔室的融合(胞吐作用)或内化(胞吞作用)所致。长期以来,细胞骨架和质膜动力学是分别进行研究的。然而,许多实验室的研究现在表明,在细胞表面的动态重塑过程中,Rho GTPases、它们对细胞骨架的调节以及膜运输是紧密相连的。Arf 和 Rab 依赖性的特定囊泡的胞吐作用有助于 Rho GTPases 及其调节因子靶向质膜的离散部位。Rho GTPases 调节胞吐囊泡的连接,并调节它们随后的融合。它们在不同形式的胞吞作用中也起着至关重要的作用,在这些作用中,它们参与膜结构域的分拣,以及膜烧瓶和杯子的塑形和密封。在这里,我们讨论了细胞表面动力学如何依赖于 Rho GTPases 对细胞骨架和质膜的协调。

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