Macrophage cholesterol efflux to free apoprotein A-I in C3H and C57BL/6 mice

被引:5
|
作者
Stein, O
Ben-Naim, M
Dabach, Y
Hollander, G
Stein, Y
机构
[1] Hadassah Univ Hosp, Lipid Res Lab, Div Med, IL-91120 Jerusalem, Israel
[2] Hebrew Univ Jerusalem, Hadassah Med Sch, Dept Expt Med & Canc Res, IL-91010 Jerusalem, Israel
关键词
ABCA1; reverse cholesterol transport; cyclic AMP; 9-cis-retinoic acid; LXR; RXR; 22(R)-hydroxycholesterol;
D O I
10.1006/bbrc.2002.6358
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
Cholesterol efflux from peritoneal macrophages of mice C57BL/6 susceptible and C3H resistant to atherosclerosis was compared, using apoprotein A-I as acceptor. The elicited macrophages were labeled with H-3-cholesterol and cholesterol enriched by incubation for 24 h with acetylated LDL. After incubation for 6 or 24 h, H-3-cholesterol efflux to free apoA-I (10 mug/ml) was significantly higher with macrophages derived from C3H mice compared to C57BL/6 mice. The cells were also pretreated with 0.3-0.45 mM cyclic AMP, 10 muM 9-cis-retinoic acid or 10 muM 22(R)-hydroxycholesterol, RXR and LXR ligands. Treatment with cyclic AMP, RXR, or LXR ligands, resulted in enhancement of H-3-cholesterol efflux in both strains. Under all conditions, 3 H-cholesterol efflux was significantly higher in C3H compared to C57BL/6 macrophages. In conclusion, the higher cholesterol efflux from C3H macrophages could contribute toward the resistance of this strain to diet-induced atherosclerosis despite hypercholesterolemia. (C) 2002 Elsevier Science (USA). olesterol.
引用
收藏
页码:1376 / 1381
页数:6
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