Essential role of RIG-I in the activation of endothelial cells by dengue virus

被引:52
作者
da Conceicao, Thais Moraes [1 ]
Rust, Naiara Miranda [2 ]
Egypto Rosa Berbel, Ana Carolina [2 ]
Martins, Nathalia Balthazar [3 ]
do Nascimento Santos, Carlos Antonio [3 ]
Da Poian, Andrea Thompson [1 ]
de Arruda, Luciana Barros [2 ]
机构
[1] Univ Fed Rio de Janeiro, CCS, Inst Bioquim Med, Bloco E,Lab E-018,Av Carlos Chagas Filho,373 Cida, Rio De Janeiro, RJ, Brazil
[2] Univ Fed Rio de Janeiro, CCS, Inst Microbiol Paulo de Goes, Rio De Janeiro, RJ, Brazil
[3] Inst Nacl Metrol Qualidade & Tecnol Inmetro, Programa Bioengn, Rio De Janeiro, RJ, Brazil
关键词
Dengue; Endothelial cells; RIG-I; Interferon; Proinflammatory cytokines; NECROSIS-FACTOR-ALPHA; TOLL-LIKE RECEPTORS; INDUCIBLE GENE-I; TNF-ALPHA; ADHESION MOLECULES; HEMORRHAGIC-FEVER; VASCULAR ENDOTHELIUM; CYTOKINE PRODUCTION; IMMUNE-RESPONSES; TIGHT JUNCTION;
D O I
10.1016/j.virol.2012.09.038
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Dengue virus (DENV) infection is associated to exacerbated inflammatory response and structural and functional alterations in the vascular endothelium. However, the mechanisms underlying DENV-induced endothelial cell activation and their role in the inflammatory response were not investigated so far. We demonstrated that human brain microvascular endothelial cells (HBMECs) are susceptible to DENV infection, which induces the expression of the cytoplasmic pattern recognition receptor (PRR) RIG-I. Infection of HBMECs promoted an increase in the production of type I IFN and proinflammatory cytokines, which were abolished after RIG-I silencing. DEN V-infected HBMECs also presented a higher ICAM-1 expression dependent on RIG-I activation as well. On the other hand, ablation of RIG-I did not interfere with virus replication. Our data suggest that RIG-I activation by DENV may participate in the disease pathogenesis through the modulation of cytokine release and expression of adhesion molecules, probably contributing to leukocyte recruitment and amplification of the inflammatory response. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:281 / 292
页数:12
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