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调节三磷酸腺苷结合盒转运体 A1 蛋白(ABCA1)的靶标:促进不同细胞中 ABCA1 介导的胆固醇流出。

The target of regulating the ATP-binding cassette A1 protein (ABCA1): promoting ABCA1-mediated cholesterol efflux in different cells.

机构信息

Department of Cardiology, Sun Yat-sen Memorial Hospital, University of Sun Yat-sen, Guangzhou, China.

出版信息

Curr Pharm Biotechnol. 2013;14(6):623-31. doi: 10.2174/138920101131400228.

DOI:10.2174/138920101131400228
PMID:24016265
Abstract

The ATP-binding cassette A1 (ABCA1) transporter plays a major role in the efflux of lipids by mediating the cellular transport of phospholipids and cholesterol to lipid-poor/lipid-free apolipoprotein A-I (apoA-I) particles and thereby exerting important anti-atherogenic effects. Although the mechanism whereby ABCA1 mediates cholesterol efflux is not completely understood, numerous studies have shown that, in addition to apoA-I, the expression level of the total or cell surface ABCA1 protein is a determining factor for the activity of ABCA1-mediated cholesterol efflux, and defects in ABCA1-mediated cholesterol efflux lead to various pathological conditions in different cells, including cardiovascular and metabolic disorders. It has been widely demonstrated that a growing list of natural and synthetic substances and metabolic regulators that modulate the expression of ABCA1 not only act directly on the ABCA1 gene promoter, but also occurs at the post-transcriptional level via micro-RNAs and post-translationally through the stabilization or localization of the protein. The complex regulatory network of ABCA1 results in promoting or suppressing cholesterol efflux from cells, therefore we speculate that the ABCA1 transporter is emerging as a novel therapeutic target for cardiovascular and metabolic disorders. Thus, ABCA1 is a key modulator of cellular cholesterol efflux and contributes to functional disorders in different types of cells.

摘要

ATP 结合盒转运蛋白 A1(ABCA1)在脂质外排中发挥主要作用,通过介导细胞内磷脂和胆固醇向富含脂质/无脂质载脂蛋白 A-I(apoA-I)颗粒的转运,从而发挥重要的抗动脉粥样硬化作用。尽管 ABCA1 介导胆固醇外排的机制尚不完全清楚,但许多研究表明,除了 apoA-I 外,总或细胞表面 ABCA1 蛋白的表达水平是 ABCA1 介导胆固醇外排活性的决定因素,ABCA1 介导的胆固醇外排缺陷导致不同细胞中的各种病理状况,包括心血管和代谢紊乱。已经广泛证明,越来越多的天然和合成物质以及代谢调节剂可以调节 ABCA1 的表达,这些调节剂不仅可以直接作用于 ABCA1 基因启动子,还可以通过 micro-RNAs 在转录后水平发生作用,并且通过蛋白质的稳定或定位发生在翻译后水平。ABCA1 的复杂调控网络导致促进或抑制细胞内胆固醇的外排,因此我们推测 ABCA1 转运蛋白正在成为心血管和代谢紊乱的新型治疗靶点。因此,ABCA1 是细胞胆固醇外排的关键调节剂,并导致不同类型细胞的功能障碍。

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