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诱导型一氧化氮合酶(iNOS)表达的下调与乙酰水杨酸在丙型肝炎病毒(HCV)表达细胞中的抗病毒活性有关。

Downregulation of inducible nitric oxide synthase (iNOS) expression is implicated in the antiviral activity of acetylsalicylic acid in HCV-expressing cells.

作者信息

Ríos-Ibarra Clara Patricia, Lozano-Sepulveda Sonia, Muñoz-Espinosa Linda, Rincón-Sánchez Ana Rosa, Cordova-Fletes Carlos, Rivas-Estilla Ana María G

机构信息

Department of Biochemistry and Molecular Medicine, School of Medicine, Autonomous University of Nuevo Leon, Ave. Francisco I. Madero y Ave. Gonzalitos s/n CP 64460, Col. Mitras Centro, Monterrey, Nuevo León, Mexico.

出版信息

Arch Virol. 2014 Dec;159(12):3321-8. doi: 10.1007/s00705-014-2201-5. Epub 2014 Aug 9.

Abstract

Previously, we described that acetylsalicylic acid (ASA) decreases HCV expression, but the mechanisms involved have not been clearly established. We evaluated the participation of inducible nitric oxide synthase (iNOS) in the regulation of HCV-RNA induced by ASA. Huh7 cells expressing non-structural HCV proteins were exposed to 4 mM ASA and incubated at the same times we reported HCV downregulation (24-72 h), and iNOS mRNA and protein levels were then measured by real-time PCR and Western blot, respectively. Nitric oxide levels were measured at the same time. Inhibition of iNOS mRNA by small interfering RNAs (siRNA) and activation of the iNOS gene promoter by ASA treatment were evaluated. In Huh7 replicon cells treated with ASA, we found decreased levels of iNOS mRNA, iNOS protein and nitrosylated protein levels at 48-72 h. ASA exposure also reduced the transactivation of the iNOS promoter in HCV replicon cells at 48 h, and this was partly due to the decrease in the affinity of transcription factor C/EBP-β for its binding site in the iNOS promoter. siRNA silencing of iNOS decreased HCV-RNA expression (65 %) and potentiated the antiviral effect (80 %) of ASA compared with control cells. ASA reduces iNOS expression by downregulating promoter activity, mRNA and protein levels at the same time that it decreases HCV expression. These findings suggest that the antiviral activity of ASA is mediated partially through the modulation of iNOS.

摘要

此前,我们曾描述过乙酰水杨酸(ASA)可降低丙型肝炎病毒(HCV)的表达,但其中涉及的机制尚未明确确立。我们评估了诱导型一氧化氮合酶(iNOS)在ASA诱导的HCV-RNA调控中的作用。将表达HCV非结构蛋白的Huh7细胞暴露于4 mM ASA,并在我们报道HCV下调的相同时间(24 - 72小时)进行孵育,然后分别通过实时PCR和蛋白质印迹法测量iNOS mRNA和蛋白质水平。同时测量一氧化氮水平。评估了小干扰RNA(siRNA)对iNOS mRNA的抑制作用以及ASA处理对iNOS基因启动子的激活作用。在用ASA处理的Huh7复制子细胞中,我们发现在48 - 72小时时iNOS mRNA、iNOS蛋白质和亚硝基化蛋白质水平降低。在48小时时,ASA处理还降低了HCV复制子细胞中iNOS启动子的反式激活,这部分是由于转录因子C/EBP-β与其在iNOS启动子中的结合位点的亲和力降低所致。与对照细胞相比,iNOS的siRNA沉默降低了HCV-RNA表达(65%)并增强了ASA的抗病毒作用(80%)。ASA在降低HCV表达的同时,通过下调启动子活性、mRNA和蛋白质水平来降低iNOS表达。这些发现表明,ASA的抗病毒活性部分是通过对iNOS的调节介导的。

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