Enhanced expression of osteopontin by high glucose in cultured rat aortic smooth muscle cells

被引:46
作者
Takemoto, M
Yokote, K
Yamazaki, M
Ridall, AL
Butler, WT
Matsumoto, T
Tamura, K
Saito, Y
Mori, S
机构
[1] Chiba Univ, Sch Med, Dept Internal Med 2, Chuo Ku, Chiba 2600856, Japan
[2] Chiba Univ, Sch Med, Dept Orthoped, Chuo Ku, Chiba 2600856, Japan
[3] Univ Texas, Hlth Sci Ctr, Dept Basic Sci, Houston, TX 77030 USA
[4] Univ Texas, Hlth Sci Ctr, Dept Prosthodont, Dent Branch, Houston, TX 77030 USA
关键词
D O I
10.1006/bbrc.1999.0701
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
Atherosclerotic vascular disease is a major complication of diabetic patients, and osteopontin has recently been implicated in the development of atherosclerosis. In the present study, we have investigated the effects of high glucose on expression of osteopontin in cultured rat aortic smooth muscle cells. High concentrations of glucose increased osteopontin secretion from the cells, and the increased secretion was completely inhibited by an inhibitor of protein kinase C, GF109203X Northern blot analysis confirmed the enhanced effect of glucose on expression of osteopontin mRNA. Promoter activity of osteopontin, measured using the osteopontin promoter/luciferase expression vector system, was increased by high glucose, and the enhanced effect was completely inhibited by GF109203X. Glucosamine also increased the promoter activity of osteopontin, and azaserine, an inhibitor of glutamine:ftuctose-6-phosphate amidotransferase (the key enzyme of the hexosamine pathway), profoundly inhibited high glucose-mediated increase in the promoter activity. Taken together, these data indicate that high glucose enhances the expression of osteopontin at the transcriptional level possibly through the activation of protein kinase C as well as the hexosamine pathway. Our results suggest that osteopontin could play a role in the development of diabetic vascular complications. (C) 1999 Academic Press.
引用
收藏
页码:722 / 726
页数:5
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