DNA-PK is a DNA sensor for IRF-3-dependent innate immunity

被引:334
作者
Ferguson, Brian J. [1 ,2 ]
Mansur, Daniel S. [1 ]
Peters, Nicholas E. [1 ]
Ren, Hongwei [1 ,2 ]
Smith, Geoffrey L. [1 ,2 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Virol, London, England
[2] Univ Cambridge, Dept Pathol, Cambridge CB2 1QP, England
来源
ELIFE | 2012年 / 1卷
基金
英国惠康基金; 英国医学研究理事会;
关键词
DEPENDENT PROTEIN-KINASE; NEUTROPHIL EXTRACELLULAR TRAPS; INTRACELLULAR DNA; CYTOSOLIC DNA; V(D)J RECOMBINATION; AUTOIMMUNE-DISEASE; CYTOPLASMIC DNA; DAI DLM-1/ZBP1; MAMMALIAN DNA; IN-VIVO;
D O I
10.7554/eLife.00047
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Innate immunity is the first immunological defence against pathogens. During virus infection detection of nucleic acids is crucial for the inflammatory response. Here we identify DNA-dependent protein kinase (DNA-PK) as a DNA sensor that activates innate immunity. We show that DNA-PK acts as a pattern recognition receptor, binding cytoplasmic DNA and triggering the transcription of type I interferon (IFN), cytokine and chemokine genes in a manner dependent on IFN regulatory factor 3 (IRF-3), TANK-binding kinase 1 (TBK1) and stimulator of interferon genes (STING). Both cells and mice lacking DNA-PKcs show attenuated cytokine responses to both DNA and DNA viruses but not to RNA or RNA virus infection. DNA-PK has well-established functions in the DNA repair and V(D)J recombination, hence loss of DNA-PK leads to severe combined immunodeficiency (SCID). However, we now define a novel anti-microbial function for DNA-PK, a finding with implications for host defence, vaccine development and autoimmunity.
引用
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页数:17
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