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DNA-PK is a DNA sensor for IRF-3-dependent innate immunity
被引:324
|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:
英国医学研究理事会;
英国惠康基金;
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.
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页数:17
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