Cellular cholesterol substrate pools for adenosine-triphosphate cassette transporter A1-dependent high-density lipoprotein formation

被引:21
作者
Boadu, Emmanuel [1 ,2 ]
Bilbey, Nicolas J. [1 ,2 ]
Francis, Gordon A. [1 ,2 ]
机构
[1] Univ British Columbia, James Hogg iCAPTURE Ctr Cardiovasc & Pulm Res, Vancouver, BC, Canada
[2] Univ British Columbia, Div Endocrinol & Metab, Dept Med, Vancouver, BC, Canada
关键词
apolipoprotein Al; ATP-binding cassette transporter A1; cholesterol; efflux; HDL;
D O I
10.1097/MOL.0b013e3282feea99
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Purpose of review The removal of cellular cholesterol and phospholipids to apolipoprotein A-I (apoA-l), facilitated by the membrane transporter ATP-binding cassette transporter A1 (ABCA1), is the rate-limiting step in the formation of high density lipoprotein particles. This review summarizes recent literature concerning the relative contributions of different cellular pools of cholesterol used by ABCA1 in the initial lipidation of apoA-l for high density lipoprotein particle formation. Recent findings Cell culture studies have shown that apart from lipidating apoA-l directly, ABCA1 can also mediate cholesterol delivery indirectly to apoA-l in the plasma membrane. Moreover, it is now clear that the late endosome/lysosome pool of cholesterol is a critical part of the total cholesterol substrate pool for ABCA1. Internalization of ABCA1 appears to be a requirement for maximum ABCA1-mediated cholesterol mobilization for high density lipoprotein formation. Summary Current evidence suggests that ABCA1-mediated cholesterol efflux to apoA-l involves mobilization of cholesterol from plasma membrane, endoplasmic reticulum, trans-Golgi network, late endocytic and lysosomal compartments, and cholesteryl ester droplets. Apart from lipidating apoA-l directly, ABCA-1 has also been found to efflux cholesterol indirectly to apoA-l in plasma membranes.
引用
收藏
页码:270 / 276
页数:7
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