Cholesterol:: Coupling between membrane microenvironment and ABC transporter activity

被引:63
作者
dos Santos, Sascha Meyer [1 ]
Weber, Claudia-Carolin [1 ]
Franke, Cornelia [1 ]
Mueller, Walter E. [1 ]
Eckert, Gunter P. [1 ]
机构
[1] Goethe Univ Frankfurt, Bioctr Niederursel, ZAFES, Dept Pharmacol, Frankfurt, Germany
关键词
lipid raft; ABC transporter; ABCB1; DRM; Pgp; cholesterol; membrane; fluidity;
D O I
10.1016/j.bbrc.2006.12.202
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Lipid composition of biological membranes is closely related to the function of the ATP-binding cassette (ABC) transporter P-Glycoprotein (Pgp). Herein, we studied how membrane physico-chemical properties affect Pgp-activity. We effectively modulated the cellular cholesterol content using methyl-beta-cyclodextrin (M beta CD) and M beta CD-cholesterol-inclusion complex. Pgp was not liberated from the plasma membrane during cholesterol modulation and functional inhibition of Pgp was related to varying cholesterol levels in the plasma membrane. Our data indicate that membrane fluidity does not solely account for cholesterol dependent modifications of Pgp-activity. Therefore, we isolated lipid rafts and examined distinct membrane microdomains. Both depletion and cholesterol enrichment induces a disassembly of lipid rafts. In cholesterol-depleted cell membranes a shift in the Pgp localisation to detergent soluble fractions was observed. Enrichment of membrane cholesterol changed lipid raft distribution but not the localisation of Pgp. From our data we conclude that Pgp-transport capacity depends on accurate lipid raft properties. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:216 / 221
页数:6
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