THE PROTECTIVE ROLE OF HIGH-DENSITY-LIPOPROTEIN ON OXDIZED-LOW-DENSITY-LIPOPROTEIN-INDUCED U937/ENDOTHELIAL CELL-INTERACTIONS

被引:54
作者
MAIER, JAM
BARENGHI, L
PAGANI, F
BRADAMANTE, S
COMI, P
RAGNOTTI, G
机构
[1] FDN RIVETTI,BIOCHEM & MOLEC BIOL LAB,MILAN,ITALY
[2] UNIV MILAN,CNR,CTR SPECIALI SISTEMI ORGAN,MILAN,ITALY
[3] UNIV MILAN,CHAIR GEN PATHOL,MILAN,ITALY
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 1994年 / 221卷 / 01期
关键词
D O I
10.1111/j.1432-1033.1994.tb18712.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The adherence of monocytes to the endothelium is an early event in atherogenesis. We have investigated this process by examining whether native and oxidized low-density and high-density lipoproteins could modulate this process. Only oxidized low-density lipoprotein caused a significant dose-dependent and time-dependent increase in U937 monocyte-like cell line binding to human endothelial cells, by a process which required de novo protein synthesis. Interestingly, E-selectin, intercellular adhesion molecule-1, vascular cell-adhesion molecule or P-selectin induction was not apparent in this system suggesting the presence of an alternative system for the interaction of endothelial cells with monocyte-like cells in response to oxidized low-density Lipoprotein. High-density lipoprotein completely suppressed oxidized low-density-lipoprotein-induced adhesion of U937 cells to the endothelial monolayer, while oxidized high-density lipoprotein did not. These data suggest that the balance between native and oxidized lipoproteins may play a role in the formation of the atherosclerotic lesion by modulating monocyte endothelial interactions.
引用
收藏
页码:35 / 41
页数:7
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