Heinecke J W, Rosen H, Chait A
J Clin Invest. 1984 Nov;74(5):1890-4. doi: 10.1172/JCI111609.
Modification of low density lipoproteins by human arterial smooth muscle cells was characterized by increased electrophoretic mobility and increased content of malondialdehyde-like oxidation products reactive with thiobarbituric acid. Lipoprotein modification was promoted by micromolar concentrations of iron or copper in the culture medium and was metal ion concentration- and time-dependent. The ability of diverse media to promote smooth muscle cell-mediated low density lipoprotein modification correlated with their iron concentration. Therefore, metal ion concentration of culture media contributes substantially to low density lipoprotein modification in vitro. Human monocyte-derived macrophages took up and esterified the cholesterol from modified low density lipoprotein more extensively than from native low density lipoprotein. Metal ion-mediated modification of low density lipoprotein may be a contributing factor to the pathogenesis of arteriosclerosis.
人动脉平滑肌细胞对低密度脂蛋白的修饰表现为电泳迁移率增加以及与硫代巴比妥酸反应的丙二醛样氧化产物含量增加。培养基中微摩尔浓度的铁或铜可促进脂蛋白修饰,且其修饰作用呈金属离子浓度和时间依赖性。不同培养基促进平滑肌细胞介导的低密度脂蛋白修饰的能力与其铁浓度相关。因此,培养基中的金属离子浓度在很大程度上促成了体外低密度脂蛋白的修饰。人单核细胞衍生的巨噬细胞从修饰的低密度脂蛋白中摄取和酯化胆固醇的程度比从天然低密度脂蛋白中摄取和酯化胆固醇的程度更大。金属离子介导的低密度脂蛋白修饰可能是动脉粥样硬化发病机制中的一个促成因素。