Antioxidants inhibit the expression of intercellular cell adhesion molecule-1 and vascular cell adhesion molecule-1 induced by oxidized LDL on human umbilical vein endothelial cells

被引:200
作者
Cominacini, L
Garbin, U
Fratta Pasini, A
Davoli, A
Campagnola, M
Contessi, GB
Pastorino, AM
LoCascio, V
机构
[1] GLAXO SPA, GLAXO RES LABS, I-37135 VERONA, ITALY
[2] UNIV VERONA, IST SEMEIOT & NEFROL MED, I-37100 VERONA, ITALY
关键词
adhesion molecules; antioxidants; atherosclerosis; free radical; human umbilical vein endothelial cells (HUVECs); intercellular cell adhesion molecule-1 (ICAM-1); oxidized LDL; vascular cell adhesion molecule-1 (VCAM-1);
D O I
10.1016/S0891-5849(96)00271-7
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 oxidative modification of low density lipoprotein (LDL) and the endothelial expression of adhesion molecules are key events in the pathogenesis of atherosclerosis, In this study we evaluated the effect of oxidized LDL on the expression of intercellular cell adhesion molecule-1 (ICAM-1), vascular cell adhesion molecule-1 (VCAM-1), and E-selectin on human umbilical vein endothelial cells (HUVECs). The hypothesis that oxidized LDL functions as a prooxidant signal was also evaluated, by studying the effect of different radical-scavenging antioxidants on expression of adhesion molecules. LDL was oxidized by using CU2+, HUVECS or phospholipase A(2) (PLA(2))/soybean lipoxygenase (SLO), the degree of oxidation being measured as thiobarbituric acid-reactive substances (TEARS) and conjugated dienes (CD). Exposure of 200 mu g/ml of native LDL to 1 mu m Cu2+, HUVECs and to PLA(2)/SLO resulted in four- to fivefold higher levels of TEARS and CD than in native LDL. CU2+-(1 mu M), HUVEC-, and PLA(2)/SLO-oxidized LDL caused a dose-dependent, significant increase of ICAM-1 and VCAM-1 (p <.01). The expression of E-selectin did not change. LDL oxidized with a 2.5 and 5 mu M CU2+ did not increase ICAM-1 and VCAM-1 significantly. Both the CU2+-and HUVEC-oxidized LDL, subjected to dialysis and ultrafiltration, induced ICAM-1 and VCAM-1 expression. After incubation with the ultrafiltrate, the expression of ICAM-1 and VCAM-1 was not significantly different from that obtained with native LDL. LDL pretreated with different antioxidants (vitamin E and probucol) and subjected to oxidation by CU2+ and HUVECs induced a significantly lower expression of ICAM-1 and VCAM-1 than nonloaded LDL (p <.01). The pretreatment of HUVECs with vitamin E and probucol significantly reduced the expression of VCAM-1 on HUVECs induced by oxidized LDL (p <.01); the effect on ICAM-1 was much less evident. In conclusion, oxidized LDL can induce the expression of different adhesion molecules on HUVECs; this induction can be prevented by pretreating either the LDL or the cells with radical-scavenging antioxidant. Copyright (C) 1996 Elsevier Science Inc.
引用
收藏
页码:117 / 127
页数:11
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