Tangier disease: still more questions than answers

被引:56
作者
Nofer, JR
Remaley, AT
机构
[1] Univ Munster, Inst Klin Chem & Lab Med, D-48129 Munster, Germany
[2] Univ Munster, Inst Arterioskleroseforsch, D-48129 Munster, Germany
[3] NIH, Dept Lab Med, Warren Grant Magnuson Clin Ctr, Bethesda, MD 20892 USA
关键词
Tangier disease; high-density lipoprotein (HDL); arteriosclerosis; reverse cholesterol transport; cholesterol efflux; ATP-binding cassette transporter 1 (ABCA1);
D O I
10.1007/s00018-005-5125-0
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
High-density lipoproteins (HDLs) play a central role in transporting cholesterol from peripheral tissues to the liver for elimination from the body. Impairment of HDL-mediated cholesterol transport favors cholesterol deposition in the arterial wall and promotes development of arteriosclerosis. Tangier disease is a severe HDL deficiency syndrome characterized by the accumulation of cholesterol in tissue macrophages and prevalent atherosclerosis. A three-decade search for a culprit in Tangier disease led to the identification of mutations in a cell membrane protein called ABCA1, which mediates the secretion of excess cholesterol from cells into the HDL metabolic pathway. Because of its ability to deplete cells of cholesterol and to raise plasma HDL levels, ABCA1 has become a promising therapeutic target for preventing cardiovascular disease.
引用
收藏
页码:2150 / 2160
页数:11
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