Hoppe G, O'Neil J, Sayre L M, Hoff H F
Department of Cell Biology, Cleveland Clinic Foundation, OH 44195, USA.
Biochim Biophys Acta. 1997 Dec 31;1362(2-3):103-8. doi: 10.1016/s0925-4439(97)00091-4.
To define the structural and chemical criteria governing recognition of oxidized LDL (oxLDL) by mouse peritoneal macrophages (MPM), we exposed LDL to novel chemical modification agents that induce defined neutralizing and non-neutralizing alterations of lysine as models for distinct apoB adducts present in oxLDL. We found some exceptions to the usual notion that neutralization of lysine positive charges is the principal determinant governing MPM recognition. In addition, competitive binding experiments using chemically modified 125I-LDL preparations revealed that, whereas some modifications engendered recognition principally by the classical scavenger receptor class A (SRA), as seen for acetylated LDL (acLDL), chemical models of advanced aldehydic modifications of LDL led instead to MPM uptake mainly by oxLDL receptors distinct from SRA.
为了确定小鼠腹腔巨噬细胞(MPM)识别氧化低密度脂蛋白(oxLDL)的结构和化学标准,我们将低密度脂蛋白(LDL)暴露于新型化学修饰剂中,这些修饰剂可诱导赖氨酸发生特定的中和及非中和改变,以此作为oxLDL中不同载脂蛋白B加合物的模型。我们发现,通常认为赖氨酸正电荷的中和是决定MPM识别的主要因素这一观点存在一些例外情况。此外,使用化学修饰的125I-LDL制剂进行的竞争性结合实验表明,虽然某些修饰主要通过经典的A类清道夫受体(SRA)引起识别,如乙酰化低密度脂蛋白(acLDL)的情况,但LDL晚期醛修饰的化学模型反而导致MPM主要通过不同于SRA的oxLDL受体摄取。