Wang X, Greilberger J, Jürgens G
Institute of Medical Biochemistry, Karl-Franzens Universität Graz, Graz, A-8010, Austria.
Anal Biochem. 1999 Feb 15;267(2):271-8. doi: 10.1006/abio.1998.3023.
Europium-labeled native and oxidized low-density lipoprotein (LDL) were used to measure their binding and cell association to mouse peritoneal macrophages, to suspended human monocyte cell line THP-1 cells, and to differentiated THP-1 macrophages. Cell binding and association were concentration dependent and saturable and showed the characteristics of ligand-receptor interaction. The validity of this assay was also supported by comparison with the method using 125iodine-labeled LDL. This nonradioactive assay proved to be specific, sensitive and simple and avoided any potential lipid peroxidation of LDL brought about by labeling lipoproteins with the widely used radioactive iodine. The latter fact is very important in studying lipoprotein-receptor interactions.
使用铕标记的天然和氧化型低密度脂蛋白(LDL)来测量它们与小鼠腹腔巨噬细胞、悬浮的人单核细胞系THP-1细胞以及分化的THP-1巨噬细胞的结合和细胞关联。细胞结合和关联呈浓度依赖性且具有饱和性,并表现出配体-受体相互作用的特征。与使用125碘标记的LDL的方法进行比较,也支持了该检测方法的有效性。这种非放射性检测方法被证明具有特异性、敏感性和简便性,并且避免了用广泛使用的放射性碘标记脂蛋白所导致的LDL任何潜在的脂质过氧化。后一事实在研究脂蛋白-受体相互作用中非常重要。