Diabetes enhances lectin-like oxidized LDL receptor-1 (LOX-1) expression in the vascular endothelium: Possible role of LOX-1 ligand and AGE

被引:118
作者
Chen, MY
Nagase, M
Fujita, T
Narumiya, S
Masaki, T
Sawamura, T [1 ]
机构
[1] Natl Cardiovasc Ctr, Res Inst, Osaka 5658565, Japan
[2] Kyoto Univ, Fac Med, Dept Pharmacol, Kyoto 606, Japan
[3] Univ Tokyo, Sch Med, Dept Internal Med 4, Tokyo 112, Japan
[4] Osaka Univ, Grad Sch Pharmaceut Sci, Dept Mol Pathophysiol, Suita, Osaka 5650871, Japan
关键词
LOX-1; endothelium; diabetes mellitus; OxLDL; advanced glycation endproducts; atherosclerosis;
D O I
10.1006/bbrc.2001.5674
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
Diabetes mellitus accelerating atherosclerosis was associated with the enhanced glycoxidative modification of lipoproteins. LOX-1, the endothelial oxidized LDL receptor might be involved in the pathogenesis of diabetic atherosclerosis. In this study, we examined the vascular expression of LOX-1 in streptozotocin-induced diabetic rats. We found that LOX-1 was significantly increased in diabetic rat aorta compared with nondiabetic control. Immunohistochemistry revealed that the most distinctive staining of LOX-1 was in the endothelial cells, especially in the bifurcations of artery branches from aorta. In cultured aortic endothelial cells, diabetic rat serum and advanced glycation endproducts-BSA induced LOX-1 expression, while control rat serum along with high glucose did not. Applying a competitive inhibition assay, we found that LOX-1 ligand activity was accumulated in the diabetic rat serum, mainly in VLDL/AML fractions. In addition, VLDL/ADL prominently increased LOX-1 among all the lipoprotein fractions of diabetic rat serum. In conclusion, diabetes markedly upregulated LOX-1 expression in the aortic endothelial cells. The enhanced glycoxidative modification of lipoproteins may contribute to the underlying mechanisms. (C) 2001 Academic Press.
引用
收藏
页码:962 / 968
页数:7
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