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质膜微区:组织、功能与运输

Plasma membrane microdomains: organization, function and trafficking.

作者信息

Laude Alex J, Prior Ian A

机构信息

The Physiological Laboratory, University of Liverpool, Liverpool, UK.

出版信息

Mol Membr Biol. 2004 May-Jun;21(3):193-205. doi: 10.1080/09687680410001700517.

Abstract

The plasma membrane consists of a mosaic of functional microdomains facilitating a variety of physiological processes associated with the cell surface. In most cells, the majority of the cell surface is morphologically featureless, leading to difficulties in characterizing its organization and microdomain composition. The reliance on indirect and perturbing techniques has led to vigorous debate concerning the nature and even existence of some microdomains. Recently, increasing technical sophistication has been applied to study cell surface compartmentalization providing evidence for small, short-lived clusters that may be much less than 50 nm in diameter. Lipid rafts and caveolae are cholesterol-dependent, highly ordered microdomains that have received most attention in recent years, yet their precise roles in regulating functions such as cell signalling remain to be determined. Endocytosis of lipid rafts/caveolae follows a clathrin-independent route to both early endosomes and non-classical caveosomes. The observation that a variety of cellular pathogens localize to and internalize with these microdomains provides an additional incentive to characterize the organization, dynamics and functions of these domains.

摘要

质膜由功能性微区镶嵌而成,这些微区促进了与细胞表面相关的多种生理过程。在大多数细胞中,大部分细胞表面在形态上没有特征,这导致在表征其组织和微区组成方面存在困难。对间接和干扰技术的依赖引发了关于某些微区的性质甚至存在与否的激烈争论。最近,越来越复杂的技术被应用于研究细胞表面区室化,为直径可能远小于50纳米的小的、短暂存在的簇提供了证据。脂筏和小窝是依赖胆固醇的、高度有序的微区,近年来受到了最多关注,但其在调节细胞信号传导等功能中的精确作用仍有待确定。脂筏/小窝的内吞作用遵循一条不依赖网格蛋白的途径,进入早期内体和非经典的小窝体。多种细胞病原体定位于这些微区并与之一起内化的观察结果,为表征这些区域的组织、动态和功能提供了额外的动力。

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