Monge J C, Hoeg J M, Law S W, Brewer H B
Molecular Disease Branch, National Heart, Lung and Blood Institute, Bethesda, MD 20892.
FEBS Lett. 1989 Jan 30;243(2):213-7. doi: 10.1016/0014-5793(89)80132-2.
We have utilized the human hepatocellular carcinoma cell line, Hep G2, to study the effects of low density lipoproteins (LDL), high density lipoproteins (HDL), and free cholesterol on apolipoprotein (apo) A-I mRNA levels. Incubation of the Hep G2 cells with LDL and free cholesterol led to a significant increase in the cellular content of cholesterol without any effect on the yield of total RNA or in the cellular protein content. Our studies established that incubation with LDL or free cholesterol increased the relative levels of apoA-I mRNA in the Hep G2 cells. In contrast with cholesterol loading, HDL had the effect of lowering the levels of apoA-I mRNA. These results indicate the LDL and HDL pathways as well as intracellular cholesterol may be important in apoA-I gene expression and regulation.
我们利用人肝癌细胞系Hep G2来研究低密度脂蛋白(LDL)、高密度脂蛋白(HDL)和游离胆固醇对载脂蛋白(apo)A-I mRNA水平的影响。用LDL和游离胆固醇孵育Hep G2细胞会导致细胞内胆固醇含量显著增加,但对总RNA产量或细胞蛋白质含量没有影响。我们的研究表明,用LDL或游离胆固醇孵育会增加Hep G2细胞中apoA-I mRNA的相对水平。与胆固醇加载相反,HDL具有降低apoA-I mRNA水平的作用。这些结果表明,LDL和HDL途径以及细胞内胆固醇可能在apoA-I基因表达和调控中起重要作用。