ADP-ribosylation factor (ARF)-like 7 (ARL7) is induced by cholesterol loading and participates in apolipoprotein AI-dependent cholesterol export

被引:56
作者
Engel, T
Lueken, A
Bode, G
Hobohm, U
Lorkowski, S
Schlueter, B
Rust, S
Cullen, P
Pech, M
Assmann, G
Seedorf, U
机构
[1] Univ Munster, Inst Arterioskleroseforsch, D-48149 Munster, Germany
[2] Univ Munster, Inst Klin Chem & Lab Med, D-48149 Munster, Germany
[3] F Hoffmann La Roche & Cie AG, Preclin Res, CH-4060 Basel, Switzerland
关键词
ADP-ribosylation factor; ras-related; ADP-ribosylation factor-like 7; GTPase; cholesterol; transport;
D O I
10.1016/j.febslet.2004.04.048
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
Here, we identify ADP-ribosylation factor (ARF)-like 7 (ARL7) as the only ARF- and ARL-family member whose mRNA-expression is induced by liver X-receptor/retinoid X- receptor agonists or cholesterol loading in human macrophages. Moreover, subcellular distribution of mutant and wild type ARL7-enhanced green fluorescent protein (EGFP) supports that ARL7 may be involved in a vesicular transport step between a perinuclear compartment and the plasma membrane. Therefore, we investigated the effect of ARL7 over-expression on the cholesterol secretory pathway. We found that expression of wild type and dominant active ARL7-EGFP stimulated the rate of apolipoprotein AI-specific cholesterol efflux 1.7- and 2.8-fold. In contrast, expression of the dominant negative form of ARL7-EGFP led to similar to50% inhibition of cholesterol efflux. This data is consistent with a model in which ARL7 is involved in transport between a perinuclear compartment and the plasma membrane apparently linked to the ABCA1-mediated cholesterol secretion pathway. (C) 2004 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:241 / 246
页数:6
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