Translation inhibition and stress granules in the antiviral immune response

被引:267
作者
McCormick, Craig [1 ]
Khaperskyy, Denys A. [1 ]
机构
[1] Dalhousie Univ, Dept Microbiol & Immunol, Halifax, NS B3H 4R2, Canada
基金
加拿大自然科学与工程研究理事会; 加拿大健康研究院;
关键词
PROTEIN-KINASE R; MESSENGER-RNA TRANSLATION; FACTOR 2-ALPHA KINASE; BINDING-PROTEINS; EBOLA-VIRUS; ACTIVATION; INITIATION; PKR; PHOSPHORYLATION; INFECTION;
D O I
10.1038/nri.2017.63
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Efficient viral gene expression is threatened by cellular stress response programmes that rapidly reprioritize the translation machinery in response to varied environmental assaults, including virus infection. This results in inhibition of bulk synthesis of housekeeping proteins and causes the aggregation of messenger ribonucleoprotein complexes into cytoplasmic foci that are known as stress granules, which can entrap viral mRNAs. There is accumulating evidence for the antiviral nature of stress granules, which is supported by the discovery of many viral factors that interfere with stress granule formation and/or function. This Review focuses on recent advances in our understanding of the role of translation inhibition and stress granules in antiviral immune responses.
引用
收藏
页码:647 / 660
页数:14
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