Rufail Miguel L, Ramage Samuel C, van Antwerpen Rik
Department of Biochemistry, Virginia Commonwealth University, Medical College of Virginia Campus, Richmond, 23298, USA.
FEBS Lett. 2006 Oct 2;580(22):5155-60. doi: 10.1016/j.febslet.2006.08.045. Epub 2006 Sep 1.
C-reactive protein (CRP) is elevated in cardiovascular disease and binds to oxidized phosphatidylcholine (oxPtC) in the low-density lipoprotein (LDL) surface. In the present study, we tested if CRP influences the susceptibility of LDL to oxidation. At physiological concentrations of 1-7mug/ml, CRP strongly inhibited copper-mediated oxidation of LDL and phospholipid liposomes in a concentration-dependent manner. Similar concentrations of different monoclonal antibodies or albumin did not influence LDL oxidation. Antioxidant activity of CRP was inhibited by phosphocholine (PC), indicating that the observed activity involves binding of CRP to oxPtC. These results suggest that CRP may limit atherogenic oxidation of LDL in vivo.
C反应蛋白(CRP)在心血管疾病中升高,并与低密度脂蛋白(LDL)表面的氧化磷脂酰胆碱(oxPtC)结合。在本研究中,我们测试了CRP是否影响LDL的氧化敏感性。在1-7μg/ml的生理浓度下,CRP以浓度依赖性方式强烈抑制铜介导的LDL和磷脂脂质体的氧化。相似浓度的不同单克隆抗体或白蛋白不影响LDL氧化。CRP的抗氧化活性被磷酸胆碱(PC)抑制,表明观察到的活性涉及CRP与oxPtC的结合。这些结果提示CRP可能在体内限制LDL的致动脉粥样硬化氧化。