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细胞间黏附中的浮舰蛋白——从细胞生理学到人类疾病

Flotillins in intercellular adhesion - from cellular physiology to human diseases.

作者信息

Bodin Stéphane, Planchon Damien, Rios Morris Eduardo, Comunale Franck, Gauthier-Rouvière Cécile

机构信息

Equipe Labellisée Ligue Contre le Cancer, Universités Montpellier 2 et 1, CRBM, CNRS, UMR 5237, 1919 Route de Mende, 34293 Montpellier, France

Equipe Labellisée Ligue Contre le Cancer, Universités Montpellier 2 et 1, CRBM, CNRS, UMR 5237, 1919 Route de Mende, 34293 Montpellier, France.

出版信息

J Cell Sci. 2014 Dec 15;127(Pt 24):5139-47. doi: 10.1242/jcs.159764. Epub 2014 Nov 20.

Abstract

Flotillin 1 and 2 are ubiquitous and highly conserved proteins. They were initially discovered in 1997 as being associated with specific caveolin-independent cholesterol- and glycosphingolipid-enriched membrane microdomains and as being expressed during axon regeneration. Flotillins have a role in a large number of physiopathological processes, mainly through their function in membrane receptor clustering and in the regulation of clathrin-independent endocytosis. In this Commentary, we summarize the research performed so far on the role of flotillins in cell-cell adhesion. Recent studies have demonstrated that flotillins directly regulate the formation of cadherin complexes. Indeed, flotillin microdomains are required for the dynamic association and stabilization of cadherins at cell-cell junctions and also for cadherin signaling. Moreover, because flotillins regulate endocytosis and also the actin cytoskeleton, they could have an indirect role in the assembly and stabilization of cadherin complexes. Because it has also recently been shown that flotillins are overexpressed during neurodegenerative diseases and in human cancers, where their upregulation is associated with metastasis formation and poor prognosis, understanding to what extent flotillin upregulation participates in the development of such pathologies is thus of particular interest, as well as how, at the molecular level, it might affect cell adhesion processes.

摘要

小窝蛋白1和2是普遍存在且高度保守的蛋白质。它们最初于1997年被发现,与特定的不依赖小窝蛋白的富含胆固醇和糖鞘脂的膜微结构域相关,并且在轴突再生过程中表达。小窝蛋白在大量生理病理过程中发挥作用,主要是通过其在膜受体聚集以及非网格蛋白依赖性内吞作用调节方面的功能。在本述评中,我们总结了迄今为止关于小窝蛋白在细胞间黏附中作用的研究。最近的研究表明,小窝蛋白直接调节钙黏蛋白复合物的形成。实际上,小窝蛋白微结构域对于钙黏蛋白在细胞间连接处的动态结合和稳定以及钙黏蛋白信号传导都是必需的。此外,由于小窝蛋白调节内吞作用以及肌动蛋白细胞骨架,它们可能在钙黏蛋白复合物的组装和稳定中发挥间接作用。因为最近还表明,小窝蛋白在神经退行性疾病和人类癌症中过度表达,其上调与转移形成和不良预后相关,所以了解小窝蛋白上调在这些病理发展中参与的程度以及它在分子水平上如何影响细胞黏附过程就特别有趣了。

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