Cutting Edge: TLR-Dependent Viral Recognition Along with Type I IFN Positive Feedback Signaling Masks the Requirement of Viral Replication for IFN-α Production in Plasmacytoid Dendritic Cells

被引:77
|
作者
Kumagai, Yutaro [1 ,2 ,3 ]
Kumar, Himanshu [1 ,2 ]
Koyama, Shohei [1 ,2 ]
Kawai, Taro [1 ,2 ]
Takeuchi, Osamu [1 ,2 ]
Akira, Shizuo [1 ,2 ,3 ]
机构
[1] Osaka Univ, Host Def Lab, World Premier Int Immunol Frontier Res Ctr, Suita, Osaka 5650871, Japan
[2] Osaka Univ, Dept Host Def, Microbial Dis Res Inst, Suita, Osaka 5650871, Japan
[3] Osaka Univ, Global Ctr Excellence Program, Frontier Biomed Sci Underlying Organelle Network, Suita, Osaka 5650871, Japan
来源
JOURNAL OF IMMUNOLOGY | 2009年 / 182卷 / 07期
基金
日本学术振兴会; 美国国家卫生研究院;
关键词
TANK-BINDING KINASE-1; IMMUNE-RESPONSES; RNA VIRUSES; RIG-I; INTERFERON; INDUCTION; INNATE; INFECTION; GENES;
D O I
10.4049/jimmunol.0804315
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Plasmacytoid dendritic cells (pDCs) recognize RNA virus infection via TLRs and consequently produce vast amounts of type I IFN. Because nucleic acid-sensing TLRs reside in the intracellular membrane compartment, it is presumable that pDCs do not require cytoplasmic viral replication to recognize the infection. By checking Newcastle disease virus (NDV) RNA abundance in GFP(+) and GFP(-) pDCs from Ifna6gfp mice, we found that NDV replication was not detected in IFN-producing pDCs. GFP(+) pDC was induced in response to replication-incompetent NDV. In contrast, the replication-incompetent NDV failed to induce IFN-producing pDCs in type I IFNR-deficient mice. The lack of IFNR signaling led to the replication of NDV and the subsequent RIG-I-like helicase-dependent IFN-alpha production in pDCs. These results showed that detection of viruses via TLRs together with a type I IFN feedback system circumvents the requirement for viral replication-dependent recognition in pDCs. The Journal of Immunology, 2009, 182: 3960-3964.
引用
收藏
页码:3960 / 3964
页数:5
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