Genetic background determines the extent of atherosclerosis in ApoE-deficient mice

被引:153
作者
Dansky, HM
Charlton, SA
Sikes, JL
Heath, SC
Simantov, R
Levin, LF
Shu, P
Moore, KJ
Breslow, JL
Smith, JD
机构
[1] Rockefeller Univ, Biochem Genet & Metab Lab, New York, NY 10021 USA
[2] Rockefeller Univ, Lab Stat Genet, New York, NY 10021 USA
[3] Cornell Univ Med Coll, Div Hematol Oncol, New York, NY USA
[4] Cornell Univ Med Coll, Div Cardiol, Dept Med, New York, NY USA
[5] Millennium Pharmaceut Inc, Cambridge, MA USA
关键词
hypercholesterolemia; lipoproteins; apolipoproteins; intercross; oxidation;
D O I
10.1161/01.ATV.19.8.1960
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Two strains of ApoE-deficient mice were found to have markedly different plasma lipoprotein profiles and susceptibility to atherosclerosis when fed either a low-fat chow or a high-fat Western-type diet. FVB/NJ ApoE-deficient (FVB EO) mice had higher total cholesterol, HDL cholesterol, ApoA1, and ApoA2 levels when compared with C57BL/6J ApoE-deficient (C57 EO) mice. At 16 weeks of age, mean aortic root atherosclerotic lesion area was 7- to 9-fold higher in chow diet-fed C57 EO mice and 3.5-fold higher in Western diet-fed C57 EO mice compared with FVB EO mice fed similar diets. Lesion area in chow diet-fed first-generation mice from a strain intercross was intermediate in size compared with parental values. The distribution of the lesion area in 150 chow diet-fed second-generation progeny spanned the range of the lesion area in both parental strains. There were no correlations between total cholesterol, non-HDL cholesterol, HDL cholesterol, ApoA1, ApoA2, ApoJ, or anti-cardiolipin antibodies and lesion area in the second-generation progeny. Thus, a genomic approach may succeed in identifying the genes responsible for the variation in atherosclerosis susceptibility in these 2 strains of ApoE-deficient mice, which could not: be explained by measured plasma parameters.
引用
收藏
页码:1960 / 1968
页数:9
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