Cross-talk between group IIA-phospholipase A2 and inducible NO-synthase in rat renal mesangial cells

被引:27
作者
Rupprecht, G
Scholz, K
Beck, KF
Geiger, H
Pfeilschifter, J
Kaszkin, M
机构
[1] Klinikum Johann Wolfgang Goethe Univ, Med Klin 4, Funkt Bereich Nephrol, D-60590 Frankfurt, Germany
[2] Klinikum Johann Wolfgang Goethe Univ, Zentrum Pharmakol, D-60590 Frankfurt, Germany
关键词
cyclic GMP; phospholipase A(2); inducible NO synthase; mesangial cells; NO-donors; signal transduction;
D O I
10.1038/sj.bjp.0702500
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1 Features of glomerulonephritis are expression of the inducible form of NO synthase (iNOS) as well as expression of the secretory group IIA-phospholipase A(2) (sPLA(2)) in mesangial cells. Interleukin 1 beta (IL-1 beta) induces both enzymes with a similar time course resulting in an increase in nitrite production and sPLA(2)-IIA activity. In this study we investigated the relationship between the formation of NO and sPLA(2)-IIA induction in rat renal mesangial cells. 2 Incubation of mesangial cells with the NO-donor, spermine-NONOate, for 24 h induced sPLA(2)-IIA mRNA expression and activity, whereas S-nitroso glutathione alone had only a small stimulatory effect. Stimulation of cells with IL-IB caused a marked increase in sPLA(2)-IIA mRNA and activity that were potentiated 3 fold by both NO donors. 3 Coincubation of cells with IL-1 beta and the NOS inhibitor, L-N-G monomethylarginine (L-NMMA), caused a dose-dependent inhibition of cytokine-induced sPLA(2)-IIA mRNA expression and activity. 4 sPLA(2)-IIA activity was not stimulated by 8-bromo-cyclic GMP indicating that NO-induced sPLA(2)-IIA induction is independent of cyclic GMP-mediated signal transduction. 5 These data show that NO contributes to the expression by cytokines of sPLA(2)-IIA and establishes a novel type of interaction between iNOS and sPLA(2)-IIA in mesangial cells. This cross-talk between inflammatory mediators may help to promote and sustain an inflammatory state in the kidney.
引用
收藏
页码:51 / 56
页数:6
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