Bergt C, Reicher H, Malle E, Sattler W
Institute of Medical Biochemistry, University Graz, Austria.
FEBS Lett. 1999 Jun 11;452(3):295-300. doi: 10.1016/s0014-5793(99)00677-8.
The present study was aimed at investigating effects of hypochlorite (HOCl) modification of high density lipoproteins subclass 3 (HDL3) on their ability for cellular cholesterol removal from permanent J774 macrophages. Our findings indicate that HOCl (added as reagent or generated enzymatically by the myeloperoxidase/H2O2/Cl- system) damages apolipoprotein A-I, the major protein component of HDL3. Fatty acid analysis of native and HOCl-modified HDL3 revealed that unsaturated fatty acids in both major lipid subclasses (phospholipids and cholesteryl esters) are targets for HOCl attack. HOCl modification resulted in impaired HDL3-mediated cholesterol efflux from J774 cells, regardless of whether reagent or enzymatically generated HOCl was used to modify the lipoprotein. Decreased cholesterol efflux was also observed after HOCl modification of reconstituted HDL particles. Impairment of cholesterol efflux from macrophages was noticed at low and physiologically occurring HOCl concentrations.
本研究旨在调查次氯酸盐(HOCl)对高密度脂蛋白亚类3(HDL3)的修饰作用对其从永久性J774巨噬细胞中清除细胞胆固醇能力的影响。我们的研究结果表明,HOCl(作为试剂添加或由髓过氧化物酶/H2O2/Cl-系统酶促产生)会损害HDL3的主要蛋白质成分载脂蛋白A-I。对天然和HOCl修饰的HDL3进行脂肪酸分析发现,两个主要脂质亚类(磷脂和胆固醇酯)中的不饱和脂肪酸都是HOCl攻击的目标。无论使用试剂还是酶促产生的HOCl来修饰脂蛋白,HOCl修饰都会导致HDL3介导的J774细胞胆固醇流出受损。在对重组HDL颗粒进行HOCl修饰后,也观察到胆固醇流出减少。在低浓度和生理浓度的HOCl下,巨噬细胞的胆固醇流出均受到损害。