DDX19A Senses Viral RNA and Mediates NLRP3-Dependent Inflammasome Activation

被引:83
作者
Li, Jiangnan [1 ]
Hu, Liang [1 ]
Liu, Yuanyuan [1 ]
Huang, Li [1 ]
Mu, Yang [2 ]
Cai, Xuehui [1 ]
Weng, Changjiang [1 ]
机构
[1] Chinese Acad Agr Sci, State Key Lab Vet Biotechnol, Harbin Vet Res Inst, Harbin 150001, Heilongjiang, Peoples R China
[2] Northwest A&F Univ, Vet Immunol Res Inst Northwest A&F Univ, Coll Vet Med, Yangling 712100, Shanxi, Peoples R China
基金
中国国家自然科学基金; 黑龙江省自然科学基金;
关键词
RESPIRATORY SYNDROME VIRUS; NOD-LIKE RECEPTORS; NLRP3; INFLAMMASOME; EXPERIMENTAL-INFECTION; IMMUNE-RESPONSES; INFLUENZA-VIRUS; RIG-I; HELICASE; REPLICATION; RECOGNITION;
D O I
10.4049/jimmunol.1501606
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The NLRP3 inflammasome plays a major role in innate immune responses by activating caspase-1, resulting in secretion of IL-1 beta and inflammatory pathologic responses. Viral RNA can induce NLRP3 inflammasome activation. However, none of the components of NLRP3 inflammasome has the ability to bind viral RNA. Therefore, it had been proposed that there might have been some unidentified cytosolic RNA sensors that could bind viral RNA and NLRP3 to initiate NLRP3 inflammasome activation. In this study, DDX19A, a member of the DEAD/H-box protein family, was identified as a novel component of NLRP3 inflammasome using arterivirus infection as a model. We found that DDX19A interacted with viral RNA and NLRP3. Knockdown of DDX19A expression efficiently inhibited procaspase-1 cleavage and IL-1 beta secretion in porcine reproductive and respiration syndrome virus (PRRSV)-infected or PRRSV RNA-stimulated primary porcine alveolar macrophages. Overall, DDX19A was identified as a novel cytosolic RNA sensor that bridged PRRSV RNA and NLRP3 to activate NLRP3 inflammasome.
引用
收藏
页码:5732 / 5749
页数:18
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