Qian Liping, Zuo Yibo, Deng Wenjun, Miao Ying, Liu Jin, Yuan Yukang, Guo Tingting, Zhang Liting, Jin Jun, Wang Jun, Zheng Hui
Institutes of Biology and Medical Sciences, Soochow University, Suzhou, Jiangsu Province, 215123, China; Jiangsu Key Laboratory of Infection and Immunity, Soochow University, Suzhou, Jiangsu Province, 215123, China.
Department of Intensive Care Medicine, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu Province, 215123, China.
Biochem Biophys Res Commun. 2018 Apr 15;498(4):891-897. doi: 10.1016/j.bbrc.2018.03.076. Epub 2018 Mar 17.
Type-I interferons (IFN-I) are widely used for antiviral immunotherapy in clinic. Therefore, identification of the regulators of IFN-I antiviral activity is important for developing novel targets for IFN-based antiviral therapy. Monocyte chemoattractant protein 1-induced protein 1 (MCPIP1) is critical for cellular inflammatory responses. However, the roles of MCPIP1 in interferons (IFNs)-mediated antiviral immunity are unexplored. In this study, we demonstrate for the first time that MCPIP1 is an important positive regulator of IFNs antiviral activity. We found that MCPIP1 can promote innate antiviral immunity independently of both its RNase and deubiquitinase activity. Furthermore, we reveal that MCPIP1 is an IFN-induced positive feedback signal molecule which promotes IFN-I-mediated antiviral efficacy. Mechanistically, MCPIP1 does not affect the activation of JAK/STAT upstream of IFN-I signaling, but significantly promotes IFN-I signaling by enhancing ISRE promoter activity and expression of interferon-stimulated genes (ISGs). And MCPIP1-mediated activation of IFN-I signaling is independently of its RNase and deubiquitinase activity. These findings uncover a novel innate antiviral mechanism mediated by the IFN-MCPIP1 axis, and may provide potential targets for enhancing IFNs antiviral therapy.
I型干扰素(IFN-I)在临床上广泛用于抗病毒免疫治疗。因此,鉴定IFN-I抗病毒活性的调节因子对于开发基于IFN的抗病毒治疗新靶点至关重要。单核细胞趋化蛋白1诱导蛋白1(MCPIP1)对细胞炎症反应至关重要。然而,MCPIP1在干扰素(IFN)介导的抗病毒免疫中的作用尚未得到探索。在本研究中,我们首次证明MCPIP1是IFN抗病毒活性的重要正调节因子。我们发现MCPIP1可以独立于其核糖核酸酶和去泛素酶活性促进先天性抗病毒免疫。此外,我们揭示MCPIP1是一种IFN诱导的正反馈信号分子,可促进IFN-I介导的抗病毒功效。从机制上讲,MCPIP1不影响IFN-I信号上游JAK/STAT的激活,但通过增强ISRE启动子活性和干扰素刺激基因(ISG)的表达来显著促进IFN-I信号传导。并且MCPIP1介导的IFN-I信号激活独立于其核糖核酸酶和去泛素酶活性。这些发现揭示了一种由IFN-MCPIP1轴介导的新型先天性抗病毒机制,并可能为增强IFN抗病毒治疗提供潜在靶点。