Role of group II secretory phospholipase A2 in atherosclerosis -: 1.: Increased atherogenesis and altered lipoproteins in transgenic mice expressing group IIa phospholipase A2

被引:203
作者
Ivandic, B
Castellani, LW
Wang, XP
Qiao, JH
Mehrabian, M
Navab, M
Fogelman, AM
Grass, DS
Swanson, ME
de Beer, MC
de Beer, F
Lusis, AJ [1 ]
机构
[1] Univ Calif Los Angeles, Sch Med, Dept Med, Div Cardiol, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Dept Microbiol & Mol Genet, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Inst Mol Biol, Los Angeles, CA 90095 USA
[4] Chrysalis DNX Transgen Sci, Princeton, NJ USA
[5] Univ Kentucky, Dept Internal Med & Biochem, Lexington, KY USA
关键词
inflammation; lipoproteins; paraoxonase;
D O I
10.1161/01.ATV.19.5.1284
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Some observations have suggested that the extracellular group IIa phospholipase A(2) (sPLA(2)), previously implicated in chronic inflammatory conditions such as arthritis, may contribute to atherosclerosis. We have examined this hypothesis by studying transgenic mice expressing the human enzyme. Compared with nontransgenic littermates, the transgenic mice exhibited dramatically increased atherosclerotic lesions when maintained on a high-fat, high-cholesterol diet. Surprisingly, the transgenic mice also exhibited significant atherosclerotic lesions when maintained on a low-fat chow diet. Immunohistochemical staining indicated that sPLA(2) was present in the atherosclerotic lesions of the transgenic mice. On both chow and atherogenic diets, the transgenic mice exhibited decreased levels of HDLs and slightly increased levels of LDLs compared with nontransgenic littermates. These data indicate that group IIa sPLA(2) may promote atherogenesis, in part, through its effects on lipoprotein levels. These data also provide a possible mechanism for the observation that there is an increased incidence of coronary artery disease in many chronic inflammatory diseases.
引用
收藏
页码:1284 / 1290
页数:7
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