SEVERE HYPERCHOLESTEROLEMIA AND ATHEROSCLEROSIS IN APOLIPOPROTEIN-E-DEFICIENT MICE CREATED BY HOMOLOGOUS RECOMBINATION IN ES CELLS

被引:1924
作者
PLUMP, AS [1 ]
SMITH, JD [1 ]
HAYEK, T [1 ]
AALTOSETALA, K [1 ]
WALSH, A [1 ]
VERSTUYFT, JG [1 ]
RUBIN, EM [1 ]
BRESLOW, JL [1 ]
机构
[1] LAWRENCE BERKELEY LAB, DIV LIFE SCI, BERKELEY, CA 94720 USA
关键词
D O I
10.1016/0092-8674(92)90362-G
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
apoE-deficient mice have been created by homologous recombination in ES cells. On a low fat, low cholesterol chow diet these animals have plasma cholesterol levels of 494 mg/dl compared with 60 mg/dl in control animals, and when challenged with a high fat Western-type diet, these animals have plasma cholesterol levels of 1821 mg/dl compared with 132 mg/dl in controls. This marked hypercholesterolemia is primarily due to elevated levels of very low and intermediate density lipoproteins. At 10 weeks of age, apoE-deficient mice have already developed atherosclerotic lesions in the aorta and coronary and pulmonary arteries. apoE-deficient mice are a promising small animal model to help understand the role of apoE in vivo and the genetic and environmental determinants of atherosclerosis.
引用
收藏
页码:343 / 353
页数:11
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