Jing Huiyuan, Zhou Yanrong, Fang Liurong, Ding Zhen, Wang Dang, Ke Wenting, Chen Huanchun, Xiao Shaobo
State Key Laboratory of Agricultural Microbiology, College of Veterinary Medicine, Huazhong Agricultural University, Wuhan, China.
Key Laboratory of Preventive Veterinary Medicine in Hubei Province, The Cooperative Innovation Center for Sustainable Pig Production, Wuhan, China.
Front Immunol. 2017 Oct 23;8:1365. doi: 10.3389/fimmu.2017.01365. eCollection 2017.
DExD/H-box helicase 36 (DHX36) is known to be an ATP-dependent RNA helicase that unwinds the guanine-quadruplexes DNA or RNA, but emerging data suggest that it also functions as pattern recognition receptor in innate immunity. Porcine reproductive and respiratory syndrome virus (PRRSV) is an that has been devastating the swine industry worldwide. Interstitial pneumonia is considered to be one of the most obvious clinical signs of PRRSV infection, suggesting that the inflammatory response plays an important role in PRRSV pathogenesis. However, whether DHX36 is involved in PRRSV-induced inflammatory cytokine expression remains unclear. In this study, we found that PRRSV infection increased the expression of DHX36. Knockdown of DHX36 and its adaptor myeloid differentiation primary response gene 88 (MyD88) by small-interfering RNA in MARC-145 cells significantly reduced NF-κB activation and pro-inflammatory cytokine expression after PRRSV infection. Further investigation revealed that PRRSV nucleocapsid protein interacted with the N-terminal quadruplex binding domain of DHX36, which in turn augmented nucleocapsid protein-induced NF-κB activation. Taken together, our results suggest that DHX36-MyD88 has a relevant role in the recognition of PRRSV nucleocapsid protein and in the subsequent activation of pro-inflammatory NF-κB pathway.
已知解旋酶DExD/H盒36(DHX36)是一种依赖ATP的RNA解旋酶,可解开鸟嘌呤四链体DNA或RNA,但新出现的数据表明,它在先天免疫中也作为模式识别受体发挥作用。猪繁殖与呼吸综合征病毒(PRRSV)是一种给全球养猪业带来巨大破坏的病毒。间质性肺炎被认为是PRRSV感染最明显的临床症状之一,这表明炎症反应在PRRSV发病机制中起重要作用。然而,DHX36是否参与PRRSV诱导的炎性细胞因子表达仍不清楚。在本研究中,我们发现PRRSV感染会增加DHX36的表达。在MARC-145细胞中,通过小干扰RNA敲低DHX36及其衔接蛋白髓样分化初级反应基因88(MyD88),可显著降低PRRSV感染后NF-κB的激活和促炎细胞因子的表达。进一步研究表明,PRRSV核衣壳蛋白与DHX36的N端四链体结合结构域相互作用,进而增强核衣壳蛋白诱导的NF-κB激活。综上所述,我们的结果表明,DHX36-MyD88在识别PRRSV核衣壳蛋白以及随后激活促炎NF-κB途径中具有相关作用。