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丙型肝炎病毒核心蛋白通过TRAF2-IKKβ依赖途径增强肿瘤坏死因子-α诱导的核因子-κB激活。

Hepatitis C virus core protein potentiates TNF-alpha-induced NF-kappaB activation through TRAF2-IKKbeta-dependent pathway.

作者信息

Chung Y M, Park K J, Choi S Y, Hwang S B, Lee S Y

机构信息

Division of Molecular Life Sciences and Center for Cell Signaling Research, Ewha Womans University, Seoul, 120-750, Korea.

出版信息

Biochem Biophys Res Commun. 2001 Jun 1;284(1):15-9. doi: 10.1006/bbrc.2001.4936.

Abstract

Previous work has implicated that the core protein of hepatitis C virus (HCV) may play a modulatory effect on NF-kappaB activation induced by TNF-alpha. However, it is unclear how HCV core protein modulates TNF-alpha-induced NK-kappaB activation. Here we show that overexpression of HCV core protein potentiates NF-kappaB activation induced by TNF-alpha. Expression of dominant negative form of TRAF2 inhibits the synergistic effects of HCV core protein on NF-kappaB activation, suggesting that HCV core protein potentiates NF-kappaB activation through TRAF2. Moreover, we demonstrate that HCV core protein potentiates TRAF2-mediated NF-kappaB activation via IKKbeta. In addition, HCV core protein associates with TNF-R1-TRADD-TRAF2 signaling complex, resulting in synergistically activation of NF-kappaB induced by TNF-alpha. Thus, these observations indicate that HCV core protein may play an important role in the regulation of the cellular inflammatory and immune responses through NF-kappaB.

摘要

先前的研究表明,丙型肝炎病毒(HCV)的核心蛋白可能对肿瘤坏死因子-α(TNF-α)诱导的核因子-κB(NF-κB)激活具有调节作用。然而,HCV核心蛋白如何调节TNF-α诱导的NF-κB激活尚不清楚。在此我们表明,HCV核心蛋白的过表达增强了TNF-α诱导的NF-κB激活。TRAF2显性负性形式的表达抑制了HCV核心蛋白对NF-κB激活的协同作用,这表明HCV核心蛋白通过TRAF2增强NF-κB激活。此外,我们证明HCV核心蛋白通过IKKβ增强TRAF2介导的NF-κB激活。另外,HCV核心蛋白与TNF-R1-TRADD-TRAF2信号复合物结合,导致TNF-α诱导的NF-κB协同激活。因此,这些观察结果表明,HCV核心蛋白可能通过NF-κB在细胞炎症和免疫反应的调节中发挥重要作用。

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