Role of HDL, LCAT, and Lipid Transfer Protein in Lipoprotein Metabolism
Role of HDL, LCAT, and Lipid Transfer Protein in Lipoprotein Metabolism
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HDL、LCAT 和脂质转移蛋白在脂蛋白代谢中的作用
DOI:
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发表时间:
1985
期刊:
影响因子:
--
通讯作者:
J. Albers
中科院分区:
文献类型:
--
作者:
J. Albers
High density lipoproteins (HDL) play an integral part in the lipid transport system. Numerous epidemiological studies have demonstrated an inverse relationship between HDL levels and the risk of developing coronary heart disease. The biochemical and physiological mechanisms behind this inverse relationship are unclear. It has been postulated that HDL, together with the enzyme lecithin cholesterol acyltransferase (LCAT) and a neutral lipid transfer protein, plays a key role in removing unesterified cholesterol from extrahepatic tissues, including the arterial wall, and in transporting it to the liver. This "reverse cholesterol transport process" is believed to prevent lipid accumulation in the artery wall and thereby prevent or retard atherogenesis. However, the specific steps and details of this reverse cholesterol transport process are controversial or remain to be clarified. The first step in this process involves the transfer of unesterified cholesterol from the surface of peripheral cells to the surface of HDL (Fig. 1). Recent evidence suggests that this transfer step may be enhanced by binding of HDL to the cell surface1). It has been postulated that peripheral cells synthesize specific, cell-surface receptors for HDL in response to cholesterol accumulation and that these receptors may act to facilitate cholesterol transport from cells2). Because HDL particles can bind only a finite number of unesterified cholesterol molecules, step 2, or the conversion of unesterified cholesterol to cholesteryl ester by LCAT, is required to keep the chemical potential gradient going. In order to remove the excess cholesteryl ester, step 3, or the transport of cholesteryl ester
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DOI:
10.1016/s0021-9258(18)89023-8
发表时间:
1985-05
期刊:
The Journal of biological chemistry
影响因子:
--
作者:
P. Subbaiah;C. Chen;J. Bagdade;J. Albers
通讯作者:
P. Subbaiah;C. Chen;J. Bagdade;J. Albers
DOI:
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发表时间:
1985
期刊:
The Journal of biological chemistry
影响因子:
--
作者:
Tollefson,JH;Faust,R;Albers,JJ;Chait,A
通讯作者:
Chait,A
影响因子:
15.9
作者:
BIESBROECK, R;ORAM, JF;BIERMAN, EL
通讯作者:
BIERMAN, EL
DOI:
--
发表时间:
1984-10
期刊:
The Journal of biological chemistry
影响因子:
--
作者:
M. Cheung;J. Albers
通讯作者:
M. Cheung;J. Albers
影响因子:
6.5
作者:
M. Cheung;J. Albers
通讯作者:
M. Cheung;J. Albers