Oxidized low density lipoprotein inhibits inducible nitric oxide synthase, GTP cyclohydrolase I and transforming growth factor β gene expression in rat macrophages

被引:0
作者
Dulak, J [1 ]
Polus, M [1 ]
Guevara, I [1 ]
Hartwich, J [1 ]
Wybranska, I [1 ]
Krzesz, R [1 ]
Dembinska-Kiec, A [1 ]
机构
[1] Jagiellonian Univ, Dept Clin Biochem, Collegium Medicum, PL-31501 Krakow, Poland
来源
JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY | 1999年 / 50卷 / 03期
关键词
LDL; inducible nitric oxide synthase; nitric oxide; GTP-cyclohydrolase I; TGF beta; atherosclerosis;
D O I
暂无
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Several studies have already demonstrated that oxidized- LDL decreases nitric oxide (NO) generation by cytokine-stimulated macrophages. However, the mechanisms of such an inhibition have not been yet elucidated. NO generation by inducible nitric oxide synthase (iNOS) is dependent on the presence of cofactors for NO generation, tetrathydrobiopterin (BH4) among them. The NO generation by these cells is also regulated by some endogenous inhibitors, like TGF-beta. Therefore, the aim of our recent study was to investigate the influence of ox-LDL on the expression of iNOS and GTP cyclohydrolase I(GTP-CH I), the key enzyme involved in the BH, synthesis as well as the ox-LDL effect on TGF-beta expression in rat macrophages stimulated with IFN gamma (250 U/ml) and LPS (500 ng/ml). Macrophages, activated in this way, express iNOS, GTP-CH I, and TGF-beta mRNA. This expression was inhibited when the macrophages were preincubated for 24 hours with ox-LDL (100 mu g/ml). Quantitative PCR revealed about 10-fold inhibition of iNOS gene expression by ox-LDL. As a consequence of down-regulation of iNOS and GTP-CH I genes, almost 3-fold diminished generation of NO2- by rat macrophages was observed. An inhibition of the TGF beta mRNA expression was also found. Our studies indicate that decreased NO generation by ox-LDL treated macrophages may be the result of the diminished expression of both iNOS and GTP-CH I genes. This effect may be mediated by the activity of certain endogenous inhibitors of gene expression, however, our studies exclude the TGF-beta as a candidate for this activity.
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页码:429 / 441
页数:13
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