SEVERE ATHEROSCLEROSIS IN TRANSGENIC MICE EXPRESSING SIMIAN CHOLESTERYL ESTER TRANSFER PROTEIN

被引:422
作者
MAROTTI, KR
CASTLE, CK
BOYLE, TP
LIN, AH
MURRAY, RW
MELCHIOR, GW
机构
[1] Molecular Biology Research and Metabolic Diseases Research, Upjohn Laboratories, 7242-209-7, Kalamazoo
关键词
D O I
10.1038/364073a0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
CHOLESTERYL ester transfer protein (CETP) is a plasma protein that mediates the exchange of neutral lipids among the lipoproteins1-3. Because the principal core lipid of very-low-density lipoprotein (VLDL) is triglyceride and that of high-density lipoprotein (HDL) is cholesterol ester, CETP mediates a 'heteroexchange' of cholesterol ester for triglyceride between those lipoproteins. As a result, animals that express CETP tend to have higher VLDL and low-density lipoprotein (LDL) cholesterol levels, whereas those with no CETP activity tend to have high HDL cholesterol levels2. Because VLDL and LDL are associated with the progression of atherosclerosis, and HDL are considered anti-atherogenic, CETP could be an 'atherogenic' protein, that is, given the other conditions required for atherosclerosis to develop, expression of CETP would accelerate the rate at which the arterial lesions progress. We report here that transgenic mice expressing CETP had much worse atherosclerosis than did non-expressing controls, and we suggest that the increase in lesion severity was due largely to CETP-induced alterations in the lipoprotein profile.
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页码:73 / 75
页数:3
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