Kunz D, Walker G, Eberhardt W, Nitsch D, Pfeilschifter J
Department of Pharmacology, Biozentrum, University of Basel, Switzerland.
Biochem Biophys Res Commun. 1995 Nov 13;216(2):438-46. doi: 10.1006/bbrc.1995.2642.
The expression of inducible nitric oxide synthase (iNOS) is triggered in rat renal mesangial cells by exposure to the inflammatory cytokine interleukin 1 beta (IL-1 beta). Here we report that cyclosporin A (CsA) a potent immunosuppressive drug, inhibits IL-1 beta dependent iNOS expression in renal mesangial cells. Addition of CsA dose dependently suppresses IL-1 beta-induced nitrite formation (IC50 = 0.9 microM). Western- and Northern blot analyses of mesangial cell extracts reveal that the inhibition of IL-1 beta-induced nitrite formation by CsA is due to decreased iNOS protein and iNOS mRNA steady state levels. Using nuclear run on experiments we show that the transcription rate of the IL-1 beta-induced iNOS gene is reduced. Furthermore, by electrophoretic mobility shift analysis we demonstrate reduced DNA-binding of the nuclear factor NF kappa B, an essential component of the IL-1 beta-dependent upregulation of iNOS gene transcription. The data presented in this report suggest that the cellular machinery involved in the IL-1 beta dependent transcriptional upregulation of the iNOS gene in mesangial cells is a target for the action of CsA.
炎症细胞因子白细胞介素1β(IL-1β)可诱导大鼠肾系膜细胞中诱导型一氧化氮合酶(iNOS)的表达。在此我们报告,强效免疫抑制药物环孢素A(CsA)可抑制肾系膜细胞中IL-1β依赖的iNOS表达。加入CsA可剂量依赖性地抑制IL-1β诱导的亚硝酸盐形成(IC50 = 0.9微摩尔)。对系膜细胞提取物进行的蛋白质印迹和Northern印迹分析表明,CsA对IL-1β诱导的亚硝酸盐形成的抑制作用是由于iNOS蛋白和iNOS mRNA稳态水平降低所致。通过细胞核转录实验我们发现,IL-1β诱导的iNOS基因转录速率降低。此外,通过电泳迁移率变动分析,我们证明核因子NF-κB的DNA结合减少,NF-κB是IL-1β依赖的iNOS基因转录上调的重要组成部分。本报告中的数据表明,参与系膜细胞中IL-1β依赖的iNOS基因转录上调的细胞机制是CsA作用的靶点。