同型半胱氨酸刺激肝细胞中胆固醇的产生和分泌

Karmin O , Edward G. Lynn , Yee H. Chung , Yaw L. Siow , Ricky Y.K. Man , P.C. Choy
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引用次数: 86

摘要

同型半胱氨酸血症和高胆固醇血症是动脉硬化性血管疾病发生的重要危险因素。在同型半胱氨酸患者和实验动物中发现血浆同型半胱氨酸和胆固醇水平呈正相关。本研究探讨了同型半胱氨酸对人肝癌细胞系HepG2细胞胆固醇产生和分泌的影响。当细胞与4 mM同型半胱氨酸孵育时,这些细胞产生的总胆固醇量和分泌的胆固醇量显著增加(从32±5 nmol/mg细胞蛋白增加到74±5 nmol/mg细胞蛋白)。进一步的生化分析表明,胆固醇的增加是由于未酯化胆固醇的产生和分泌增加,而胆固醇酯的水平没有随之变化。同型半胱氨酸孵育HepG2细胞24和48 h后,细胞内3-羟基-3-甲基戊二酰辅酶A (HMG-CoA)还原酶活性分别显著升高131%和190%,并刺激HepG2细胞分泌载脂蛋白B100(从0.84±0.11 μg /mg细胞蛋白增加到1.37±0.12 μg /mg细胞蛋白)。我们的研究结果表明,同型半胱氨酸刺激HepG2细胞中胆固醇和载脂蛋白B100的产生和分泌。同型半胱氨酸引起的胆固醇生成增加可能与动脉硬化的发病机制有关。
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Homocysteine stimulates the production and secretion of cholesterol in hepatic cells

Homocysteinemia and hypercholesterolemia are important risk factors associated with the occurrence of arteriosclerotic vascular diseases. A positive correlation between plasma levels of homocysteine and cholesterol was found in homocysteinemic patients as well as in experimental animals. In the present study, the effect of homocysteine on the production and secretion of cholesterol in human hepatoma cell line HepG2 cells was investigated. When cells were incubated with 4 mM homocysteine, the amounts of total cholesterol produced as well as the cholesterol secreted by these cells were significantly increased (from 32±5 to 74±5 nmol/mg cellular protein). Further biochemical analyses revealed that the increase in cholesterol was resulted from an enhancement in the production and secretion of the unesterified cholesterol with no concomitant change in the level of cholesteryl esters. The activity of intracellular 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase was markedly elevated by 131% and 190% after cells were incubated with homocysteine for 24 and 48 h. Homocysteine also stimulated the secretion of apo B100 by HepG2 cells (from 0.84±0.11 to 1.37±0.12 μg apolipoprotein B/mg cellular protein). Our results demonstrate that homocysteine stimulates the production and secretion of cholesterol and apolipoprotein B100 in HepG2 cells. The increase in the production of cholesterol induced by homocysteine may contribute to the pathogenesis of arteriosclerosis.

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