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哺乳动物 ABC 蛋白的脂质转运。

Lipid transport by mammalian ABC proteins.

机构信息

Department of Biochemistry and Molecular Biology, University of British Columbia, Vancouver, BC, Canada, V6T 1Z3.

出版信息

Essays Biochem. 2011 Sep 7;50(1):265-90. doi: 10.1042/bse0500265.

Abstract

ABC (ATP-binding cassette) proteins actively transport a wide variety of substrates, including peptides, amino acids, sugars, metals, drugs, vitamins and lipids, across extracellular and intracellular membranes. Of the 49 hum an ABC proteins, a significant number are known to mediate the extrusion of lipids from membranes or the flipping of membrane lipids across the bilayer to generate and maintain membrane lipid asymmetry. Typical lipid substrates include phospholipids, sterols, sphingolipids, bile acids and related lipid conjugates. Members of the ABCA subfamily of ABC transporters and other ABC proteins such as ABCB4, ABCG1 and ABCG5/8 implicated in lipid transport play important roles in diverse biological processes such as cell signalling, membrane lipid asymmetry, removal of potentially toxic compounds and metabolites, and apoptosis. The importance of these ABC lipid transporters in cell physiology is evident from the finding that mutations in the genes encoding many of these proteins are responsible for severe inherited diseases. For example, mutations in ABCA1 cause Tangier disease associated with defective efflux of cholesterol and phosphatidylcholine from the plasma membrane to the lipid acceptor protein apoA1 (apolipoprotein AI), mutations in ABCA3 cause neonatal surfactant deficiency associated with a loss in secretion of the lipid pulmonary surfactants from lungs of newborns, mutations in ABCA4 cause Stargardt macular degeneration, a retinal degenerative disease linked to the reduced clearance of retinoid compounds from photoreceptor cells, mutations in ABCA12 cause harlequin and lamellar ichthyosis, skin diseases associated with defective lipid trafficking in keratinocytes, and mutations in ABCB4 and ABCG5/ABCG8 are responsible for progressive intrafamilial hepatic disease and sitosterolaemia associated with defective phospholipid and sterol transport respectively. This chapter highlights the involvement of various mammalian ABC transporters in lipid transport in the context of their role in cell signalling, cellular homoeostasis, apoptosis and inherited disorders.

摘要

ABC(ATP 结合盒)蛋白可主动将多种底物,包括肽、氨基酸、糖、金属、药物、维生素和脂质,跨细胞外和细胞内膜转运。在 49 个人类 ABC 蛋白中,已知许多蛋白介导脂质从膜中排出,或膜脂在双层膜内翻转以产生和维持膜脂不对称性。典型的脂质底物包括磷脂、固醇、鞘脂、胆汁酸和相关脂质缀合物。ABC 转运蛋白的 ABCA 亚家族成员和其他 ABC 蛋白,如 ABCB4、ABCG1 和 ABCG5/8,它们在脂质转运中发挥重要作用,涉及多种生物学过程,如细胞信号转导、膜脂不对称性、去除潜在有毒化合物和代谢物以及细胞凋亡。这些 ABC 脂质转运蛋白在细胞生理学中的重要性,从发现编码这些蛋白的许多基因突变导致严重的遗传性疾病中可以明显看出。例如,ABCA1 基因突变导致 Tangier 病,其特征是胆固醇和磷脂酰胆碱从质膜向脂质接受蛋白 apoA1(载脂蛋白 AI)的外排缺陷;ABCA3 基因突变导致新生儿表面活性剂缺乏症,其特征是脂质肺表面活性剂从新生儿肺部的分泌丢失;ABCA4 基因突变导致 Stargardt 黄斑变性,这是一种与视黄醇化合物从光感受器细胞清除减少相关的视网膜退行性疾病;ABCA12 基因突变导致 Harlequin 和板层鱼鳞病,这是一种与角质形成细胞中脂质转运缺陷相关的皮肤病;ABCB4 和 ABCG5/ABCG8 基因突变导致进行性家族性肝内疾病和甾醇血症,分别与磷脂和固醇转运缺陷相关。本章重点介绍了各种哺乳动物 ABC 转运蛋白在细胞信号转导、细胞内稳态、细胞凋亡和遗传性疾病中的脂质转运作用。

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