Upregulation of lectin-like oxidized low-density lipoprotein receptor-1 (LOX-1) by 15-lipoxygenase-modified LDL in endothelial cells

被引:37
作者
Pirillo, Angela [1 ]
Reduzzi, Alice [1 ]
Ferri, Nicola [1 ]
Kuhn, Hartmut [2 ]
Corsini, Alberto [1 ]
Catapano, Alberico L. [1 ,3 ]
机构
[1] Univ Milan, Dept Pharmacol Sci, I-20133 Milan, Italy
[2] Charite, Inst Biochem, D-13353 Berlin, Germany
[3] IRCCS Multimed Milan, Milan, Italy
关键词
LOX-1; LDL; 15-Lipoxygenase; Endothelial cells; ICAM-1; INDUCED INFLAMMATORY RESPONSE; HUMAN ATHEROSCLEROTIC LESIONS; VASCULAR ENDOTHELIUM; SCAVENGER RECEPTORS; MONOCYTE ADHESION; DEFICIENT MICE; MESSENGER-RNA; KAPPA-B; OX-LDL; EXPRESSION;
D O I
10.1016/j.atherosclerosis.2010.11.006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Lectin-like oxidized LDL receptor-1 (LOX-1), the endothelial receptor for OxLDL, is believed to be responsible for a number of OxLDL-induced effects in the endothelium. Methods and results: In the present study we showed that LDL modified by 15-lipoxygenase (15LO-LDL), a form of minimally modified lipoprotein, beside its ability to induce pro-inflammatory responses such as oxidative stress and the expression of adhesion molecules, significantly increases LOX-1 expression in endothelial cells, both at transcriptional and at protein level. Such effect is likely to be mediated by p38 MAPK and NF-kB pathways. We then permanently overexpressed LOX-1 in an endothelial cell line and showed that 15LO-LDL were a ligand for LOX-1, and that the interaction LOX-1/15LO-LDL upregulated ICAM-1 surface expression. Conclusion: Altogether these results indicate minimally modified LDL as a new inducer for LOX-1 expression and as a new ligand for LOX-1. (C) 2010 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:331 / 337
页数:7
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