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非小窝型小窝蛋白——小窝之外的职责

Non-caveolar caveolins - duties outside the caves.

作者信息

Pol Albert, Morales-Paytuví Frederic, Bosch Marta, Parton Robert G

机构信息

Cell Compartments and Signaling Group, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Universitat de Barcelona, 08036, Barcelona, Spain

Department of Biomedical Sciences, Faculty of Medicine, Universitat de Barcelona, 08036, Barcelona, Spain.

出版信息

J Cell Sci. 2020 May 11;133(9):jcs241562. doi: 10.1242/jcs.241562.

DOI:10.1242/jcs.241562
PMID:32393675
Abstract

Caveolae are invaginations of the plasma membrane that are remarkably abundant in adipocytes, endothelial cells and muscle. Caveolae provide cells with resources for mechanoprotection, can undergo fission from the plasma membrane and can regulate a variety of signaling pathways. Caveolins are fundamental components of caveolae, but many cells, such as hepatocytes and many neurons, express caveolins without forming distinguishable caveolae. Thus, the function of caveolins goes beyond their roles as caveolar components. The membrane-organizing and -sculpting capacities of caveolins, in combination with their complex intracellular trafficking, might contribute to these additional roles. Furthermore, non-caveolar caveolins can potentially interact with proteins normally excluded from caveolae. Here, we revisit the non-canonical roles of caveolins in a variety of cellular contexts including liver, brain, lymphocytes, cilia and cancer cells, as well as consider insights from invertebrate systems. Non-caveolar caveolins can determine the intracellular fluxes of active lipids, including cholesterol and sphingolipids. Accordingly, caveolins directly or remotely control a plethora of lipid-dependent processes such as the endocytosis of specific cargoes, sorting and transport in endocytic compartments, or different signaling pathways. Indeed, loss-of-function of non-caveolar caveolins might contribute to the common phenotypes and pathologies of caveolin-deficient cells and animals.

摘要

小窝是质膜的内陷结构,在脂肪细胞、内皮细胞和肌肉中大量存在。小窝为细胞提供机械保护资源,可从质膜发生裂变,并能调节多种信号通路。小窝蛋白是小窝的基本组成成分,但许多细胞,如肝细胞和许多神经元,表达小窝蛋白却不形成可区分的小窝。因此,小窝蛋白的功能超出了它们作为小窝组成成分的作用。小窝蛋白的膜组织和塑造能力,连同其复杂的细胞内运输,可能促成了这些额外的作用。此外,非小窝型小窝蛋白可能会与通常被排除在小窝之外的蛋白质相互作用。在这里,我们重新审视小窝蛋白在包括肝脏、大脑、淋巴细胞、纤毛和癌细胞在内的多种细胞环境中的非经典作用,并探讨来自无脊椎动物系统的见解。非小窝型小窝蛋白可决定活性脂质(包括胆固醇和鞘脂)的细胞内通量。因此,小窝蛋白直接或间接控制大量脂质依赖性过程,如特定货物的内吞作用、内吞小室中的分选和运输,或不同的信号通路。事实上,非小窝型小窝蛋白的功能丧失可能导致小窝蛋白缺陷细胞和动物的常见表型和病理状况。

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