Roles of Nucleoporin RanBP2/Nup358 in Acute Necrotizing Encephalopathy Type 1 (ANE1) and Viral Infection

被引:31
作者
Jiang, Jing [1 ]
Wang, Yifan E. [2 ]
Palazzo, Alexander F. [2 ]
Shen, Qingtang [1 ]
机构
[1] Fujian Med Univ, Sch Basic Med Sci, Dept Immunol, Fuzhou 350108, Peoples R China
[2] Univ Toronto, Dept Biochem, Toronto, ON M5G 1M1, Canada
基金
加拿大健康研究院;
关键词
RanBP2; acute necrotizing encephalopathy type 1 (ANE1); viruses; cytokines; NUCLEAR-PORE COMPLEX; TUMOR-NECROSIS-FACTOR; PAPILLOMAVIRUS E1 PROTEIN; GTPASE-ACTIVATING PROTEIN; RANBP2; MUTATION; MESSENGER-RNA; CEREBROSPINAL-FLUID; SUMO-1; MODIFICATION; VIRUS INFECTION; DNA-REPLICATION;
D O I
10.3390/ijms23073548
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ran Binding Protein 2 (RanBP2 or Nucleoporin358) is one of the main components of the cytoplasmic filaments of the nuclear pore complex. Mutations in the RANBP2 gene are associated with acute necrotizing encephalopathy type 1 (ANE1), a rare condition where patients experience a sharp rise in cytokine production in response to viral infection and undergo hyperinflammation, seizures, coma, and a high rate of mortality. Despite this, it remains unclear howRanBP2 and its ANE1-associated mutations contribute to pathology. Mounting evidence has shown that RanBP2 interacts with distinct viruses to regulate viral infection. In addition, RanBP2 may regulate innate immune response pathways. This review summarizes recent advances in our understanding of how mutations in RANBP2 contribute to ANE1 and discusses how RanBP2 interacts with distinct viruses and affects viral infection. Recent findings indicate that RanBP2 might be an important therapeutic target, not only in the suppression of ANE1-driven cytokine storms, but also to combat hyperinflammation in response to viral infections.
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页数:17
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