Reduced aortic lesions and elevated high density lipoprotein levels in transgenic mice overexpressing mouse apolipoprotein A-IV

被引:150
作者
Cohen, RD
Castellani, LW
Qiao, JH
VanLenten, BJ
Lusis, AJ
Reue, K
机构
[1] W LOS ANGELES VET AFFAIRS MED CTR, LIPID RES LAB, LOS ANGELES, CA 90073 USA
[2] UNIV CALIF LOS ANGELES, DEPT MED, LOS ANGELES, CA 90095 USA
[3] UNIV CALIF LOS ANGELES, DEPT MICROBIOL & MOL GENET, LOS ANGELES, CA 90095 USA
[4] UNIV CALIF LOS ANGELES, INST MOL BIOL, LOS ANGELES, CA 90095 USA
关键词
apo A-IV; atherosclerosis; lipoproteins; cellular cholesterol efflux; transgene;
D O I
10.1172/JCI119358
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Transgenic mouse lines carrying several copies of the mouse apo A-IV gene were produced. Lipoprotein composition and function, and aortic lesion development were examined. Apo A-IV levels in the plasma of transgenic mice were elevated threefold compared with nontransgenic littermates on a chow diet, and sixfold in mice fed an atherogenic diet. Plasma concentrations of total cholesterol, HDL cholesterol, triglycerides, and free fatty acids were similar in transgenic and control mice fed a chow diet. However, with the atherogenic diet, male transgenic mice exhibited significantly higher levels of plasma triglycerides (P < 0.05), total cholesterol (P < 0.01), HDL cholesterol (P < 0.0001), and free fatty acids (P < 0.05), and lower levels of unesterified cholesterol (P < 0.05), than nontransgenic littermates. Expression of the apo A-IV transgene had a protective effect against the formation of diet-induced aortic lesions, with transgenics exhibiting lesion scores of similar to 30% those seen in control mice. HDL-sized lipoproteins isolated from transgenic mice fed the atherogenic diet promoted cholesterol efflux from cholesterol-loaded human monocytes more efficiently than comparable lipoproteins from nontransgenic counterparts. Plasma from transgenics also exhibited higher endogenous cholesterol esterification rates. Taken together, these results suggest that apo A-IV levels influence the metabolism and antiatherogenic properties of HDL.
引用
收藏
页码:1906 / 1916
页数:11
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