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三磷酸腺苷结合盒转运蛋白与胆固醇转运

ATP-binding cassette transporters and cholesterol translocation.

机构信息

Department of Pediatrics, University of Alberta, Edmonton, AB, Canada.

出版信息

IUBMB Life. 2013 Jun;65(6):505-12. doi: 10.1002/iub.1165.

Abstract

Cholesterol, a major component of mammalian cell membranes, plays important structural and functional roles. However, accumulation of excessive cholesterol is toxic to cells. Aberrant cholesterol trafficking and accumulation is the molecular basis for many diseases, such as atherosclerotic cardiovascular disease and Tangier's disease. Accumulation of excessive cholesterol is also believed to contribute to the early onset of Alzheimer's disease. Thus, cellular cholesterol homeostasis is tightly regulated by uptake, de novo synthesis, and efflux. Any surplus of cholesterol must either be stored in the cytosol in the form of esters or released from the cell. Recently, several ATP-binding cassette (ABC) transporters, such as ABCA1, ABCG1, ABCG5, and ABCG8 have been shown to play important roles in the regulation of cellular cholesterol homeostasis by mediating cholesterol efflux. Mutations in ABC transporters are associated with several human diseases. In this review, we discuss the physiological roles of ABC transporters and the underlying mechanisms by which they mediate cholesterol translocation.

摘要

胆固醇是哺乳动物细胞膜的主要成分之一,发挥着重要的结构和功能作用。然而,过量的胆固醇积累对细胞是有毒的。胆固醇运输和积累的异常是许多疾病的分子基础,如动脉粥样硬化性心血管疾病和 Tangier 病。过量胆固醇的积累也被认为是导致阿尔茨海默病早期发病的原因之一。因此,细胞内胆固醇的动态平衡受到摄取、从头合成和外排的严格调控。多余的胆固醇必须以酯的形式储存在细胞质中,或者从细胞中释放出来。最近,几种 ATP 结合盒(ABC)转运蛋白,如 ABCA1、ABCG1、ABCG5 和 ABCG8,已被证明通过介导胆固醇外排在调节细胞内胆固醇动态平衡中发挥重要作用。ABC 转运蛋白的突变与几种人类疾病有关。在这篇综述中,我们讨论了 ABC 转运蛋白的生理作用及其介导胆固醇转运的潜在机制。

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