载脂蛋白E
生物
内科学
同源重组
内分泌学
体内
主动脉
同源染色体
载脂蛋白B
重组
胆固醇
遗传学
基因
医学
疾病
作者
Andrew S. Plump,Jonathan Smith,Tony Hayek,Katriina Aalto‐Setälä,A Walsh,Judy G. Verstuyft,Edward M. Rubin,Jan L. Breslow
出处
期刊:Cell
[Cell Press]
日期:1992-10-01
卷期号:71 (2): 343-353
被引量:2122
标识
DOI:10.1016/0092-8674(92)90362-g
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.
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