Yang M, Leake D S, Rice-Evans C A
Division of Biochemistry and Molecular Biology, UMDS-Guy's Hospital, London, U.K.
Biochem J. 1996 Jun 1;316 ( Pt 2)(Pt 2):377-80. doi: 10.1042/bj3160377.
The oxidative modification of low-density lipoprotein (LDL) has been implicated in the pathogenesis of atherosclerosis, although little is known as yet about the precise mechanism of oxidation in vivo. The studies presented here demonstrate that, in the absence of cells or transition metals, oxidized LDL can modify native LDL through co-incubation in vitro such as to increase its net negative charge, in a concentration-dependent manner. The interaction is not inhibited by peroxyl radical scavengers or metal chelators, precluding the possibility that the modification of native LDL by oxidized LDL is through an oxidative process. Studies with radioiodinated oxidized LDL showed no transfer of radioactivity to the native LDL, demonstrating that fragmentation of protein and the transfer of some of the fragments does not account for the modified charge on the native LDL particle. The adjacency of native to oxidized LDL in the arterial wall may be a potential mechanism by which the altered recognition properties of the apolipoprotein B-100 may arise rapidly without oxidation or extensive modification of the native LDL lipid itself.
低密度脂蛋白(LDL)的氧化修饰与动脉粥样硬化的发病机制有关,尽管目前对体内氧化的确切机制知之甚少。此处呈现的研究表明,在没有细胞或过渡金属的情况下,氧化型LDL可通过体外共同孵育修饰天然LDL,从而以浓度依赖的方式增加其净负电荷。这种相互作用不受过氧自由基清除剂或金属螯合剂的抑制,排除了氧化型LDL对天然LDL的修饰是通过氧化过程的可能性。对放射性碘化氧化型LDL的研究表明,没有放射性转移至天然LDL,这表明蛋白质的片段化以及部分片段的转移并不能解释天然LDL颗粒上电荷的改变。动脉壁中天然LDL与氧化型LDL的相邻可能是一种潜在机制,通过该机制载脂蛋白B-100识别特性的改变可能迅速出现,而无需对天然LDL脂质本身进行氧化或广泛修饰。