HDL亚类对人成纤维细胞3-羟基-3-甲基戊二酰辅酶A还原酶的影响。

W H Daerr, S H Gianturco, J R Patsch, L C Smith, A M Gotto
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引用次数: 3

摘要

利用正常人成纤维细胞单层培养,研究高密度脂蛋白主要亚类HDL2和HDL3对3-羟基-3-甲基戊二酰辅酶a还原酶(EC 1.1.1.34)活性的影响。在该系统中,HDL3 (d = 1.125-1.210 g/cm3)特异性诱导HMG-CoA还原酶活性。对培养动力学的评价表明,酶的诱导仅限于生长的固定阶段。当HDL2 (d = 1.063-1.125 g/cm3)孵育细胞时,观察到还原酶活性受到抑制。当HDL2大于总HDL的35%时,HDL2和HDL3的混合物抑制还原酶活性。环己二酮可消除HDL2的抑制作用,精氨酸残基再生可恢复HDL2的抑制作用,提示载脂蛋白介导的抑制机制。这些观察结果表明,HDL的细胞效应取决于细胞生长阶段和通常分离的HDL中HDL亚类的比例。
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Effects of HDL subclasses on 3-hydroxy-3-methylglutaryl coenzyme A reductase in human fibroblasts.

Monolayer cultures of normal human fibroblasts were used to study the effects of the main subclasses of high-density lipoproteins, HDL2 and HDL3, on 3-hydroxy-3-methylglutaryl CoA reductase (EC 1.1.1.34) activity. In this system, HDL3 (d = 1.125-1.210 g/cm3) specifically induced HMG-CoA reductase activity. Evaluation of culture dynamics revealed that enzyme induction was restricted to the stationary phase of growth. When the cells were incubated with HDL2 (d = 1.063-1.125 g/cm3), suppression of reductase activity was observed. Mixtures of HDL2 and HDL3 suppressed reductase activity when HDL2 was greater than 35% of the total HDL. The suppressive effects of HDL2 were abolished by treatment with cyclohexanedione and restored by regeneration of the arginyl residues, suggesting an apoprotein-mediated suppressive mechanism. These observations show that the cellular effects of HDL depend upon the stage of cell growth and the ratio of HDL subclasses in HDL as usually isolated.

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