Ding Yang, Ao Jingqun, Huang Xiaohong, Chen Xinhua
Key Laboratory of Marine Biogenetic Resources, Third Institute of Oceanography, State Oceanic Administration, Xiamen, China; College of Ocean and Earth Sciences, Xiamen University, Xiamen, China.
Key Laboratory of Marine Biogenetic Resources, Third Institute of Oceanography, State Oceanic Administration , Xiamen , China.
Front Immunol. 2016 Sep 7;7:343. doi: 10.3389/fimmu.2016.00343. eCollection 2016.
Like mammals, fish possess an interferon regulatory factor (IRF) 3/IRF7-dependent type I IFN responses, but the exact mechanism by which IRF3/IRF7 regulate the type I IFNs remains largely unknown. In this study, we identified two type I IFNs in the Perciforme fish large yellow croaker Larimichthys crocea, one of which belongs to the fish IFNd subgroup and the other is assigned to a novel subgroup of group I IFNs in fish, tentatively termed IFNh. The two IFN genes are constitutively expressed in all examined tissues, but with varied expression levels. Both IFN genes can be rapidly induced in head kidney and spleen tissues by polyinosinic-polycytidylic acid. The recombinant IFNh was shown to be more potent to trigger a rapid induction of the antiviral genes MxA and protein kinase R than the IFNd, suggesting that they may play distinct roles in regulating early antiviral immunity. Strikingly, IFNd, but not IFNh, could induce the gene expression of itself and IFNh through a positive feedback loop mediated by the IFNd-dependent activation of IRF3 and IRF7. Furthermore, our data demonstrate that the induction of IFNd can be enhanced by the dimeric formation of IRF3 and IRF7, while the IFNh expression mainly involves IRF3. Taken together, our findings demonstrate that the IFN responses are diverse in fish and are likely to be regulated by distinct mechanisms.
与哺乳动物一样,鱼类拥有干扰素调节因子(IRF)3/IRF7依赖性I型干扰素反应,但IRF3/IRF7调节I型干扰素的确切机制仍不清楚。在本研究中,我们在鲈形目鱼类大黄鱼(Larimichthys crocea)中鉴定出两种I型干扰素,其中一种属于鱼类IFNd亚组,另一种被归为鱼类I型干扰素的一个新亚组,暂称为IFNh。这两种干扰素基因在所有检测组织中均组成性表达,但表达水平各异。两种干扰素基因均可被聚肌苷酸-聚胞苷酸快速诱导在头肾和脾脏组织中表达。重组IFNh比IFNd更有效地触发抗病毒基因Mx A和蛋白激酶R的快速诱导,表明它们在调节早期抗病毒免疫中可能发挥不同作用。令人惊讶的是,IFNd而非IFNh可通过由IFNd依赖性激活IRF3和IRF7介导的正反馈环诱导自身和IFNh的基因表达。此外,我们的数据表明,IRF3和IRF7的二聚体形成可增强IFNd的诱导,而IFNh的表达主要涉及IRF3。综上所述,我们的研究结果表明,鱼类中的干扰素反应具有多样性,且可能受不同机制调控。