Kisseleva A F, Medvedeva N V, Goryunova L E
Institute of Experimental Cardiology, Cardiology Research Center Moscow, Russia.
Membr Cell Biol. 2000;14(2):205-17.
The cholesteryl oleate-POPC dispersions (1:3, mol/mol, mean particle size 110+/-20 nm) were taken up by the human hepatoma line Hep G2 cells via endocytosis. Internalization of the cholesteryl oleate-POPC dispersions by Hep G2 cells was dependent on the incubation time and dispersion concentration. At the cholesteryl oleate concentration 100 microM, its total uptake and internalization were found to be 1.5 nmol and 0.8 nmol per 1 mg of cell protein/24 h, respectively. Intracellular cleavage of the cholesteryl oleate incorporated in dispersions resulted in accumulation of free cholesterol capable of being released into the medium and metabolized to water-soluble polar products, presumably bile acids; oleic acid released is, apparently, involved in biosynthesis of triacylglycerides. The low-density lipoprotein receptor is not involved in internalization of lipid dispersions, and the presence of the cholesteryl oleate-POPC dispersions has no effect on the receptor-dependent internalization of cholesteryl esters of the low-density lipoproteins. The obtained data allow us to consider nonspecific internalization of cholesteryl esters by hepatocytes as a substantial part of the nonpolar lipid clearance.
胆固醇油酸酯 - POPC 分散体(1:3,摩尔/摩尔,平均粒径 110±20 纳米)通过内吞作用被人肝癌细胞系 Hep G2 细胞摄取。Hep G2 细胞对胆固醇油酸酯 - POPC 分散体的内化作用取决于孵育时间和分散体浓度。在胆固醇油酸酯浓度为 100 μM 时,发现其每 1 mg 细胞蛋白/24 h 的总摄取量和内化量分别为 1.5 nmol 和 0.8 nmol。分散体中所含胆固醇油酸酯的细胞内裂解导致游离胆固醇积累,这些游离胆固醇能够释放到培养基中并代谢为水溶性极性产物,推测为胆汁酸;释放出的油酸显然参与三酰甘油的生物合成。低密度脂蛋白受体不参与脂质分散体的内化作用,胆固醇油酸酯 - POPC 分散体的存在对低密度脂蛋白胆固醇酯的受体依赖性内化作用没有影响。所获得的数据使我们能够将肝细胞对胆固醇酯的非特异性内化作用视为非极性脂质清除的重要组成部分。