Deng Minnan, Du Ganqin, Zhao Jiegang, Du Xiaowei
Department of Neurology, The First Affiliated Hospital, and College of Clinical Medicine of Henan University of Science and Technology, Luoyang, 471003, Henan, China.
Department of Graduate Student Section, The First Affiliated Hospital, and College of Clinical Medicine of Henan University of Science and Technology, Luoyang, 471003, Henan, China.
Arch Virol. 2017 Jun;162(6):1495-1505. doi: 10.1007/s00705-017-3226-3. Epub 2017 Feb 11.
Increasing evidence confirms the involvement of virus infection and miRNA, such as miR-146a, in neuroinflammation-associated epilepsy. In the present study, we investigated the upregulation of miR-146a with RT-qPCR and in situ hybridization methods in a mice infection model of Japanese encephalitis virus (JEV) and in vitro. Subsequently we investigated the involvement of miR-146a in modulating JEV-induced neuroinflammation. It was demonstrated that JEV infection promoted miR-146a production in BALB/c mice brain and in cultured mouse microglial C8-B4 cells, along with pro-inflammatory cytokines, such as IL-1β, IL-6, TNF-α, IFN-β and IFN-α. We also found that miR-146a exerted negative regulatory effects upon IL-1β, IL-6, TNF-α, IFN-β and IFN-α in C8-B4 cells. Accordingly, miR-146a downregulation with a miR-146a inhibitor promoted the upregulation of IL-1β, IL-6, TNF-α, IFN-β and IFN-α, whereas miR-146a upregulation with miR-146a mimics reduced the upregulation of these cytokines. Moreover, miR-146a exerted no regulation upon JEV growth in C8-B4 cells. In conclusion, JEV infection upregulated miR-146a and pro-inflammatory cytokine production, in mice brain and in cultured C8-B4 cells. Furthermore, miR-146a negatively regulated the production of JEV-induced pro-inflammatory cytokines, in virus growth independent fashion, identifying miR-146a as a negative feedback regulator in JEV-induced neuroinflammation, and possibly in epilepsy.
越来越多的证据证实病毒感染和微小RNA(如miR-146a)与神经炎症相关的癫痫有关。在本研究中,我们采用逆转录定量聚合酶链反应(RT-qPCR)和原位杂交方法,在日本脑炎病毒(JEV)小鼠感染模型及体外实验中,研究了miR-146a的上调情况。随后,我们研究了miR-146a在调节JEV诱导的神经炎症中的作用。结果表明,JEV感染促进了BALB/c小鼠脑和培养的小鼠小胶质细胞C8-B4中miR-146a的产生,同时还促进了白细胞介素-1β(IL-1β)、白细胞介素-6(IL-6)、肿瘤坏死因子-α(TNF-α)、干扰素-β(IFN-β)和干扰素-α(IFN-α)等促炎细胞因子的产生。我们还发现,miR-146a对C8-B4细胞中的IL-1β、IL-6、TNF-α、IFN-β和IFN-α发挥负调节作用。相应地,用miR-146a抑制剂下调miR-146a可促进IL-1β、IL-6、TNF-α、IFN-β和IFN-α的上调,而用miR-146a模拟物上调miR-146a则可降低这些细胞因子的上调。此外,miR-146a对C8-B4细胞中JEV的生长没有调节作用。总之,JEV感染上调了小鼠脑和培养的C8-B4细胞中miR-146a和促炎细胞因子的产生。此外,miR-146a以独立于病毒生长的方式对JEV诱导的促炎细胞因子的产生发挥负调节作用,表明miR-146a是JEV诱导的神经炎症以及可能在癫痫中起作用的负反馈调节因子。