Cholesteryl ester transfer protein (CETP) expression protects against diet induced atherosclerosis in SR-BI deficient mice

被引:43
|
作者
Harder, Christopher
Lau, Paulina
Meng, Andrew
Whitman, Stewart C.
McPherson, Ruth
机构
[1] Univ Ottawa, Inst Heart, Lipoprot & Atherosclerosis Res Grp, Ottawa, ON K1Y 4W7, Canada
[2] Univ Ottawa, Inst Heart, Div Cardiol, Ottawa, ON K1Y 4W7, Canada
关键词
CETP; SR-BI; atherosclerosis; HDL;
D O I
10.1161/01.ATV.0000259357.42089.dc
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective - To determine whether expression of the human CETP transgene protects against diet-induced atherosclerosis in SR-BI deficient mice. Methods and Results - SR-BI deficient (-/-) mice were crossed with CETP transgenic (CETPtg) mice to produce a colony of SR-BI-/- x CETPtg mice in a C57B1/6 background. Age and sex matched groups of genetically modified and wild-type C57B1/6 mice were fed a high fat, high cholesterol diet for 22 weeks. In both wild-type and SR-BI-/- mice, expression of the CETP transgene reduced the cholesterol content and increased the density of lipoprotein particles in the HDL density range. In SR-BI-/- x CETPtg mice, CETP activity inversely correlated with total plasma cholesterol levels and shifted the buoyant HDL typical of SR-BI deficiency toward a more normal density HDL particle. Atherosclerosis at the level of the aortic arch was evident in both male and female SR-BI deficient mice but occurred to a greater extent in the females. Expression of CETP markedly attenuated the development of atherosclerosis in SR-BI deficient mice fed an atherogenic diet (P < 0.003). Conclusions - Expression of the human CETP transgene protects SR-BI deficient mice from atherosclerosis, consistent with a role for CETP in remodeling HDL and providing an alternative pathway for the selective uptake of HDL-CE by the liver.
引用
收藏
页码:858 / 864
页数:7
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