Zhao Xueyan, Chu Qing, Cui Junxia, Huo Ruixuan, Xu Tianjun
Laboratory of Fish Biogenetics & Immune Evolution, College of Marine Science, Zhejiang Ocean University, Zhoushan, 316022, China.
Laboratory of Fish Biogenetics & Immune Evolution, College of Marine Science, Zhejiang Ocean University, Zhoushan, 316022, China.
Mol Immunol. 2017 May;85:123-129. doi: 10.1016/j.molimm.2017.02.009. Epub 2017 Feb 23.
Proinflammatory cytokines and type I IFNs were produced by TLR signaling and these responses are crucial for host defensive responses against pathogens. In order to avoid harmful and inappropriate inflammatory responses, there are multiple mechanisms to negatively regulate TLR signaling. In this paper, we have firstly studied IRF9 functions as a negative regulator involved in TRIF-mediated NF-κB pathway. Moreover, we found inhibitory effect of IRF9 primary depends on DBD domain. Interestingly, we also demonstrated that else mutants of IRF9, except for IRF9-ΔDBD, have different inhibitory effects upon TRIF-mediated NF-κB pathway. This study provides a novel evidence about the negatively regulation of innate immune signaling pathway in teleost fish. In addition, this finding provides new insights into the regulatory mechanism in mammals.
促炎细胞因子和I型干扰素由Toll样受体(TLR)信号产生,这些反应对于宿主抵御病原体的防御反应至关重要。为了避免有害和不适当的炎症反应,存在多种负调控TLR信号的机制。在本文中,我们首先研究了干扰素调节因子9(IRF9)作为参与TRIF介导的NF-κB途径的负调节因子的功能。此外,我们发现IRF9的抑制作用主要依赖于DNA结合结构域(DBD)。有趣的是,我们还证明,除了IRF9-ΔDBD之外,IRF9的其他突变体对TRIF介导的NF-κB途径具有不同的抑制作用。这项研究为硬骨鱼先天免疫信号通路的负调控提供了新的证据。此外,这一发现为哺乳动物的调控机制提供了新的见解。