de Vries H E, Buchner B, van Berkel T J, Kuiper J
Division of Biopharmaceutics, Leiden/Amsterdam Center for Drug Research, Sylvius Laboratories, University of Leiden, PO Box 9503, 2300 RA Leiden, The Netherlands.
Arterioscler Thromb Vasc Biol. 1999 Mar;19(3):638-45. doi: 10.1161/01.atv.19.3.638.
Interaction of oxidized LDL (OxLDL) with macrophage-derived foam cells is one of the key events in the development and progression of atherosclerosis. To study this interaction, macrophage-derived foam cells were isolated from rabbit atherosclerotic lesions and the expression of scavenger receptors for OxLDL was examined. Atherosclerosis was induced in rabbits by denudation of the large arteries, followed by a hypercholesteremic diet. Macrophage-derived foam cells, characterized by immunostaining with an RAM-11 antibody (a macrophage marker), contained a high content of intracellular lipid. Maximal binding of radiolabeled OxLDL to isolated macrophage-derived foam cells (1652+/-235 ng 125I-OxLDL/mg of cell protein) was 20-fold higher compared with Bmax values of monocytes. Levels of association of OxLDL to macrophage-derived foam cells isolated from atherosclerotic lesions 12 weeks after denudation were >3-fold higher compared with the levels expressed by macrophage-derived foam cells isolated after 6 weeks. Association of 125I-OxLDL could be completely blocked by OxLDL, and partially by acetylated LDL and polyinosinic acid, indicating the presence of a specific binding site for OxLDL on macrophage-derived foam cells. The induction of scavenger receptors for OxLDL on macrophage-derived foam cells during the development of atherosclerosis, as described in this study, may facilitate the lipid accumulation in macrophage-derived foam cells, as observed in advanced atherosclerotic lesions.
氧化型低密度脂蛋白(OxLDL)与巨噬细胞源性泡沫细胞的相互作用是动脉粥样硬化发生和发展的关键事件之一。为研究这种相互作用,从兔动脉粥样硬化病变中分离出巨噬细胞源性泡沫细胞,并检测了OxLDL清道夫受体的表达。通过剥脱大动脉内皮,随后给予高胆固醇饮食诱导兔发生动脉粥样硬化。巨噬细胞源性泡沫细胞经RAM-11抗体(一种巨噬细胞标志物)免疫染色鉴定,细胞内脂质含量高。放射性标记的OxLDL与分离的巨噬细胞源性泡沫细胞的最大结合量(1652±235 ng 125I-OxLDL/mg细胞蛋白)比单核细胞的Bmax值高20倍。与剥脱后6周分离的巨噬细胞源性泡沫细胞相比,剥脱后12周从动脉粥样硬化病变中分离的巨噬细胞源性泡沫细胞与OxLDL的结合水平高出3倍以上。125I-OxLDL的结合可被OxLDL完全阻断,被乙酰化低密度脂蛋白和聚肌苷酸部分阻断,表明巨噬细胞源性泡沫细胞上存在OxLDL的特异性结合位点。如本研究所述,在动脉粥样硬化发展过程中巨噬细胞源性泡沫细胞上OxLDL清道夫受体的诱导,可能促进了巨噬细胞源性泡沫细胞内脂质的积聚,这在晚期动脉粥样硬化病变中可见。