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

被引:44
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
相关论文
共 42 条
[1]   Cholesteryl ester transfer protein mediates selective uptake of high density lipoprotein cholesteryl esters by human adipose tissue [J].
Benoist, F ;
Lau, P ;
McDonnell, M ;
Doelle, H ;
Milne, R ;
McPherson, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (38) :23572-23577
[2]  
BLIGH EG, 1959, CAN J BIOCHEM PHYS, V37, P911
[3]  
Bruce C, 1998, J LIPID RES, V39, P1071
[4]   Scavenger receptor class B type I mediates the selective uptake of high-density lipoprotein-associated cholesteryl ester by the liver in mice [J].
Brundert, M ;
Ewert, A ;
Heeren, J ;
Behrendt, B ;
Ramakrishnan, R ;
Greten, H ;
Merkel, M ;
Rinninger, F .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2005, 25 (01) :143-148
[5]  
CALVO D, 1993, J BIOL CHEM, V268, P18929
[6]  
CAMUS MC, 1983, J LIPID RES, V24, P1210
[7]   Cholesteryl ester transfer protein corrects dysfunctional high density lipoproteins and reduces aortic atherosclerosis in lecithin cholesterol acyltransferase transgenic mice [J].
Föger, B ;
Chase, M ;
Amar, MJ ;
Vaisman, BL ;
Shamburek, RD ;
Paigen, B ;
Furchart-Najib, J ;
Paiz, JA ;
Koch, CA ;
Hoyt, RF ;
Brewer, HB ;
Santamarina-Fojo, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (52) :36912-36920
[8]   Increasing high-density lipoprotein cholesterol in dyslipidemia by cholesteryl ester transfer protein inhibition - An update for clinicians [J].
Forrester, JS ;
Makkar, R ;
Shah, PK .
CIRCULATION, 2005, 111 (14) :1847-1854
[9]   Cholesteryl ester transfer protein directly mediates selective uptake of high density lipoprotein cholesteryl esters by the liver [J].
Gauthier, A ;
Lau, P ;
Zha, XH ;
Milne, R ;
McPherson, R .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2005, 25 (10) :2177-2184
[10]   Diet and murine atherosclerosis [J].
Getz, GS ;
Reardon, CA .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2006, 26 (02) :242-249