Nassar Taher, Sachais Bruce S, Akkawi Sa'ed, Kowalska Maria Anna, Bdeir Khalil, Leitersdorf Eran, Hiss Edna, Ziporen Leah, Aviram Michael, Cines Douglas, Poncz Mortimer, Higazi Abd Al-Roof
Department of Clinical Biochemistry, the Center for Research, Prevention, and Treatment of Atherosclerosis, Hadassah University Hospital and Hebrew University-Hadassah Medical School, Jerusalem 91120, Israel.
J Biol Chem. 2003 Feb 21;278(8):6187-93. doi: 10.1074/jbc.M208894200. Epub 2002 Dec 3.
Accumulation of low-density lipoprotein (LDL)-derived cholesterol by macrophages in vessel walls is a pathogenomic feature of atherosclerotic lesions. Platelets contribute to lipid uptake by macrophages through mechanisms that are only partially understood. We have previously shown that platelet factor 4 (PF4) inhibits the binding and degradation of LDL through its receptor, a process that could promote the formation of oxidized LDL (ox-LDL). We have now characterized the effect of PF4 on the binding of ox-LDL to vascular cells and macrophages and on the accumulation of cholesterol esters. PF4 bound to ox-LDL directly and also increased ox-LDL binding to vascular cells and macrophages. PF4 did not stimulate ox-LDL binding to cells that do not synthesize glycosaminoglycans or after enzymatic cleavage of cell surface heparan and chondroitin sulfates. The effect of PF4 on binding ox-LDL was dependent on specific lysine residues in its C terminus. Addition of PF4 also caused an approximately 10-fold increase in the amount of ox-LDL esterified by macrophages. Furthermore, PF4 and ox-LDL co-localize in atherosclerotic lesion, especially in macrophage-derived foam cells. These observations offer a potential mechanism by which platelet activation at sites of vascular injury may promote the accumulation of deleterious lipoproteins and offer a new focus for pharmacological intervention in the development of atherosclerosis.
血管壁中的巨噬细胞积累低密度脂蛋白(LDL)衍生的胆固醇是动脉粥样硬化病变的病理特征。血小板通过一些仅部分为人所知的机制促进巨噬细胞摄取脂质。我们之前已表明,血小板因子4(PF4)通过其受体抑制LDL的结合和降解,这一过程可能会促进氧化型LDL(ox-LDL)的形成。我们现在已明确了PF4对ox-LDL与血管细胞及巨噬细胞结合以及胆固醇酯积累的影响。PF4直接与ox-LDL结合,还增加了ox-LDL与血管细胞及巨噬细胞的结合。PF4不会刺激ox-LDL与不合成糖胺聚糖的细胞结合,也不会在细胞表面硫酸乙酰肝素和硫酸软骨素经酶切后刺激ox-LDL与细胞结合。PF4对结合ox-LDL的影响取决于其C末端的特定赖氨酸残基。添加PF4还使巨噬细胞酯化的ox-LDL量增加了约10倍。此外,PF4和ox-LDL在动脉粥样硬化病变中共同定位,尤其是在巨噬细胞衍生的泡沫细胞中。这些观察结果提供了一种潜在机制,通过该机制血管损伤部位的血小板活化可能促进有害脂蛋白的积累,并为动脉粥样硬化发展过程中的药物干预提供了新的靶点。