Dynamic interplay between cell membrane tension and clathrin-mediated endocytosis

IF 2.4 4区 生物学 Q4 CELL BIOLOGY Biology of the Cell Pub Date : 2021-03-31 DOI:10.1111/boc.202000110
Umidahan Djakbarova, Yasaman Madraki, Emily T. Chan, Cömert Kural
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引用次数: 21

Abstract

Deformability of the plasma membrane, the outermost surface of metazoan cells, allows cells to be dynamic, mobile and flexible. Factors that affect this deformability, such as tension on the membrane, can regulate a myriad of cellular functions, including membrane resealing, cell motility, polarisation, shape maintenance, membrane area control and endocytic vesicle trafficking. This review focuses on mechanoregulation of clathrin-mediated endocytosis (CME). We first delineate the origins of cell membrane tension and the factors that yield to its spatial and temporal fluctuations within cells. We then review the recent literature demonstrating that tension on the membrane is a fast-acting and reversible regulator of CME. Finally, we discuss tension-based regulation of endocytic clathrin coat formation during physiological processes.

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细胞膜张力与网格蛋白介导的胞吞作用之间的动态相互作用
后生动物细胞最外表面的质膜具有可变形性,使细胞具有动态、可移动和柔性。影响这种可变形性的因素,如膜上的张力,可以调节无数的细胞功能,包括膜再密封、细胞运动、极化、形状维持、膜面积控制和内吞囊泡运输。本文就网格蛋白介导的胞吞作用(CME)的机制调控作一综述。我们首先描述了细胞膜张力的起源和使其在细胞内时空波动的因素。然后,我们回顾了最近的文献,证明膜上的张力是CME的快速作用和可逆的调节器。最后,我们讨论了生理过程中基于张力的内吞网格蛋白外壳形成调节。
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来源期刊
Biology of the Cell
Biology of the Cell 生物-细胞生物学
CiteScore
5.30
自引率
0.00%
发文量
53
审稿时长
>12 weeks
期刊介绍: The journal publishes original research articles and reviews on all aspects of cellular, molecular and structural biology, developmental biology, cell physiology and evolution. It will publish articles or reviews contributing to the understanding of the elementary biochemical and biophysical principles of live matter organization from the molecular, cellular and tissues scales and organisms. This includes contributions directed towards understanding biochemical and biophysical mechanisms, structure-function relationships with respect to basic cell and tissue functions, development, development/evolution relationship, morphogenesis, stem cell biology, cell biology of disease, plant cell biology, as well as contributions directed toward understanding integrated processes at the organelles, cell and tissue levels. Contributions using approaches such as high resolution imaging, live imaging, quantitative cell biology and integrated biology; as well as those using innovative genetic and epigenetic technologies, ex-vivo tissue engineering, cellular, tissue and integrated functional analysis, and quantitative biology and modeling to demonstrate original biological principles are encouraged.
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