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MLKL mediated necroptosis accelerates JEV-induced neuroinflammation in mice

  • Peiyu Bian
  • , Xuyang Zheng
  • , Li Wei
  • , Chuantao Ye
  • , Hong Fan
  • , Yanhui Cai
  • , Ying Zhang
  • , Fanglin Zhang
  • , Zhansheng Jia
  • , Yingfeng Lei
  • Tangdu Hospital, Fourth Military Medical University
  • Xijing Hospital
  • Air Force Medical University

Research output: Contribution to journalArticlepeer-review

37 Scopus citations

Abstract

Japanese encephalitis virus (JEV) is the most prevalent cause of viral encephalitis in Asia and the western Pacific. Neuronal death caused by JEV infection and inflammation induced cytotoxicity leads to progression and deterioration of Japanese encephalitis (JE). Mixed-lineage kinase domain-like protein (MLKL) mediated necroptosis is a newly discovered pathway of programmed cell death and participates in many inflammatory diseases. In this study, we demonstrated for the first time that necroptosis was involved in the neuronal loss during JE via immune-electron microscopy and immunochemistry. The expression of MLKL in neurons was upregulated in presence of JEV infection in vitro and in vivo. Deletion of MLKL alleviated the progression of JE and decreased the level of inflammatory cytokines in mice model. Taken together, this study provides evidence for the participation of necroptosis in the pathogenesis of JEV infection.

Original languageEnglish
Article number303
JournalFrontiers in Microbiology
Volume8
Issue numberFEB
DOIs
StatePublished - 28 Feb 2017
Externally publishedYes

Keywords

  • Inflammation
  • Japanese encephalitis virus
  • MLKL
  • Necroptosis
  • Neuronal death

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