Nitric oxide attenuates adhesion molecule expression in human endothelial cells

被引:87
作者
Takahashi, M
Ikeda, U
Masuyama, JI
Funayama, H
Kano, S
Shimada, K
机构
[1] JICHI MED SCH,DEPT CARDIOL,MINAMI KAWACHI,TOCHIGI 32904,JAPAN
[2] JICHI MED SCH,DEPT CLIN IMMUNOL,MINAMI KAWACHI,TOCHIGI 32904,JAPAN
关键词
interleukin; 1; ICAM-1; VCAM-1; atherosclerosis; cGMP; HUMAN ATHEROSCLEROTIC LESIONS; LEUKOCYTE ADHESION; MYOCARDIAL-ISCHEMIA; REPERFUSION; PLAQUES; ICAM-1; NO;
D O I
10.1006/cyto.1996.0109
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
Leukocyte adhesion to vascular endothelium is a crucial step in the early stages of atherosclerosis, which may be mediated by the interaction of adhesion molecules expressed on the surfaces of both cell types. in this study, we investigated the effects of nitric oxide OVO) on the expression of intercellular adhesion molecule-1 (ICAM-1) and vascular cell adhesion molecule-1 (VCAM-1) in human umbilical vein endothelial cells (HUVECs). ICAM-1 and VCAM-1 protein and mRNA expression were determined by cellular ELISA and Northern blot analysis, respectively. Both ICAM-1 and VCAM-1 expression were increased markedly by interleukin-1 beta(IL-1 beta). This IL-1 beta-mediated induction of ICAM-1 and VCAM-1 expression was significantly inhibited in the presence of a NO donor 3-morpholino-sydnonimine (SIN-1) in a dose-dependent manner. The inhibitory effect of SIN-1 was abolished in the presence of a NO scavenger haemoglobin, while addition of 8-bromo-cGMP showed no significant effect on IL-1 beta-induced ICAM-1 or VCAM-1 expression. Northern blot analysis showed that IL-1 beta markedly increased ICAM-1 and VCAM-1 mRNA expression, while SIN-1 decreased the accumulation of these transcripts induced by IL-1 beta. These results suggest that NO could prevent the focal adhesion and accumulation of leukocytes through the inhibition of ICAM-1 and VCAM-1 expression in endothelial cells. (C) 1996 Academic Press Limited.
引用
收藏
页码:817 / 821
页数:5
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