Van Lenten B J, Fogelman A M, Haberland M E, Edwards P A
Proc Natl Acad Sci U S A. 1986 Apr;83(8):2704-8. doi: 10.1073/pnas.83.8.2704.
The addition of bacterial lipopolysaccharide (LPS) from Escherichia coli 0111:B4 to human monocyte-macrophages cultured in serum results in suppression of scavenger receptor activity. The present studies were performed to examine if the effect on scavenger receptor activity was mediated by LPS alone or by LPS in association with lipoproteins. Radioiodinated LPS (125I-LPS) was added to human plasma in vitro and to normal and hyperlipidemic rabbit plasma in vitro and in vivo to determine the distribution of 125I-LPS among the lipoprotein classes. It was found that all lipoprotein classes bound LPS in direct proportion to their plasma cholesterol concentration. LPS alone was compared to LPS bound to low density lipoprotein (LDL), high density lipoprotein, or reductively-methylated LDL for their abilities to suppress scavenger receptor activity in monocyte-macrophages in lipoprotein-free serum. Only LPS bound to LDL (LPS-LDL) demonstrated an effect similar to that observed when LPS was added to cells in serum. Either unlabeled LDL or unlabeled LPS-LDL complexes competed with the uptake of 125I-LPS-LDL complexes, which appeared to proceed by receptor-mediated endocytosis. In contrast to the uptake of 125I-LDL, the uptake of 125I-LPS-LDL by cultured monocyte-macrophages was not followed by its hydrolysis and the release of its radioactive degradation products into the medium. The association of LPS with lipoproteins was very stable and appeared to be mediated by a lipid-lipid interaction. We hypothesize that LPS bound to lipoproteins may be transported into the artery wall and may initiate the atherosclerotic reaction.
将来自大肠杆菌0111:B4的细菌脂多糖(LPS)添加到在血清中培养的人单核细胞 - 巨噬细胞中会导致清道夫受体活性受到抑制。进行本研究以检查对清道夫受体活性的影响是由LPS单独介导还是由LPS与脂蛋白共同介导。将放射性碘化LPS(125I - LPS)体外添加到人血浆以及正常和高脂血症兔血浆中,并在体内添加,以确定125I - LPS在脂蛋白类别中的分布。发现所有脂蛋白类别结合LPS的量与它们的血浆胆固醇浓度成正比。将单独的LPS与结合到低密度脂蛋白(LDL)、高密度脂蛋白或还原甲基化LDL上的LPS进行比较,以观察它们在无脂蛋白血清中抑制单核细胞 - 巨噬细胞清道夫受体活性的能力。只有结合到LDL上的LPS(LPS - LDL)表现出与将LPS添加到血清中的细胞时观察到的效果相似的作用。未标记的LDL或未标记的LPS - LDL复合物与125I - LPS - LDL复合物的摄取竞争,125I - LPS - LDL复合物的摄取似乎通过受体介导的内吞作用进行。与125I - LDL的摄取不同,培养的单核细胞 - 巨噬细胞对125I - LPS - LDL的摄取之后不会发生其水解以及其放射性降解产物释放到培养基中。LPS与脂蛋白的结合非常稳定,似乎是由脂质 - 脂质相互作用介导的。我们推测结合到脂蛋白上的LPS可能被转运到动脉壁中并可能引发动脉粥样硬化反应。