Porcine reproductive and respiratory syndrome virus infection triggers HMGB1 release to promote inflammatory cytokine production

被引:31
作者
Duan, Erzhen [1 ]
Wang, Dang [1 ]
Luo, Rui [1 ]
Luo, Jingyi [1 ]
Gao, Li [1 ]
Chen, Huanchun [1 ]
Fang, Liurong [1 ]
Xiao, Shaobo [1 ]
机构
[1] Huazhong Agr Univ, Coll Vet Med, State Key Lab Agr Microbiol, Wuhan 430070, Peoples R China
基金
中国国家自然科学基金;
关键词
Porcine reproductive and respiratory syndrome virus (PRRSV); HMGB1; Cytokines; Inflammatory response; GROUP BOX 1; MOBILITY GROUP BOX-1; NF-KAPPA-B; DENDRITIC CELLS; PROTEIN HMGB1; HIGH-MOBILITY-GROUP-BOX-1; PROTEIN; HIV-1; REPLICATION; TISSUE-DAMAGE; RECEPTOR; ACTIVATION;
D O I
10.1016/j.virol.2014.07.046
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The high mobility group box 1 (HMGB1) protein is an endogenous damage-associated molecular pattern (DAMP) molecule involved in the pathogenesis of various infectious agents. Based on meta-analysis of all publicly available microarray datasets, HMGB1 has recently been proposed as the most significant immune modulator during the porcine response to porcine reproductive and respiratory syndrome virus (PRRSV) infection. However, the function of HMGB1 in PRRSV pathogenesis is unclear. In this study, we found that PRRSV infection triggers the translocation of HMGB1 from the nucleus to the extracellular milieu in MARC-145 cells and porcine alveolar macrophages. Although HMGB1 has no effect on PRRSV replication, HMGB1 promotes PRRSV-induced NF-kappa B activation and subsequent expression of inflammatory cytokines through receptors RAGE, TLR2 and TLR4. Our findings show that HMGB1 release, triggered by PRRSV infection, enhances the efficiency of virus-induced inflammatory responses, thereby providing new insights into the pathogenesis of PRRSV infection. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:1 / 9
页数:9
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