Mitochondria in innate immune responses

被引:1046
作者
West, A. Phillip [2 ]
Shadel, Gerald S. [2 ,3 ]
Ghosh, Sankar [1 ]
机构
[1] Columbia Univ, Dept Microbiol & Immunol, Coll Phys & Surg, New York, NY 10032 USA
[2] Yale Univ, Sch Med, Dept Pathol, New Haven, CT 06520 USA
[3] Yale Univ, Sch Med, Dept Genet, New Haven, CT 06520 USA
基金
美国国家卫生研究院;
关键词
NF-KAPPA-B; INTERFERON REGULATORY FACTOR-3; NLRP3 INFLAMMASOME ACTIVATION; ANTIVIRAL SIGNALING PROTEIN; RIG-I; UNCOUPLING PROTEIN-2; ADAPTER PROTEIN; ENDOPLASMIC-RETICULUM; CRYSTAL-STRUCTURE; NECROTIC CELLS;
D O I
10.1038/nri2975
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The innate immune system has a key role in the mammalian immune response. Recent research has demonstrated that mitochondria participate in a broad range of innate immune pathways, functioning as signalling platforms and contributing to effector responses. In addition to regulating antiviral signalling, mounting evidence suggests that mitochondria facilitate antibacterial immunity by generating reactive oxygen species and contribute to innate immune activation following cellular damage and stress. Therefore, in addition to their well-appreciated roles in cellular metabolism and programmed cell death, mitochondria appear to function as centrally positioned hubs in the innate immune system. Here, we review the emerging knowledge about the roles of mitochondria in innate immunity.
引用
收藏
页码:389 / 402
页数:14
相关论文
共 102 条
[1]   The role of mitochondria in cellular defense against microbial infection [J].
Arnoult, Damien ;
Carneiro, Leticia ;
Tattoli, Ivan ;
Girardin, Stephen E. .
SEMINARS IN IMMUNOLOGY, 2009, 21 (04) :223-232
[2]   An N-terminal addressing sequence targets NLRX1 to the mitochondrial matrix [J].
Arnoult, Damien ;
Soares, Fraser ;
Tattoli, Ivan ;
Castanier, Celine ;
Philpott, Dana J. ;
Girardin, Stephen E. .
JOURNAL OF CELL SCIENCE, 2009, 122 (17) :3161-3168
[3]   Disruption of the uncoupling protein-2 gene in mice reveals a role in immunity and reactive oxygen species production [J].
Arsenijevic, D ;
Onuma, H ;
Pecqueur, C ;
Raimbault, S ;
Manning, BS ;
Miroux, B ;
Couplan, E ;
Alves-Guerra, MC ;
Goubern, M ;
Surwit, R ;
Bouillaud, F ;
Richard, D ;
Collins, S ;
Ricquier, D .
NATURE GENETICS, 2000, 26 (04) :435-439
[4]   Persistent nuclear factor-κB activation in UCP2-/- mice leads to enhanced nitric oxide and inflammatory cytokine production [J].
Bai, Y ;
Onuma, H ;
Bai, X ;
Medvedev, AV ;
Misukonis, M ;
Weinberg, JB ;
Cao, WH ;
Robidoux, J ;
Floering, LM ;
Daniel, KW ;
Collins, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (19) :19062-19069
[5]   Initiation and beyond: Multiple functions of the human mitochondril transcription machinery [J].
Bonawitz, Nicholas D. ;
Clayton, David A. ;
Shadel, Gerald S. .
MOLECULAR CELL, 2006, 24 (06) :813-825
[6]   Viral evasion and subversion of pattern-recognition receptor signalling [J].
Bowie, Andrew G. ;
Unterholzner, Leonie .
NATURE REVIEWS IMMUNOLOGY, 2008, 8 (12) :911-922
[7]   Physiological functions of the mitochondrial uncoupling proteins UCP2 and UCP3 [J].
Brand, MD ;
Esteves, TC .
CELL METABOLISM, 2005, 2 (02) :85-93
[8]   Activation of host pattern recognition receptors by viruses [J].
Brennan, Kiva ;
Bowie, Andrew G. .
CURRENT OPINION IN MICROBIOLOGY, 2010, 13 (04) :503-507
[9]   MITOCHONDRIAL N-FORMYLMETHIONYL PROTEINS AS CHEMOATTRACTANTS FOR NEUTROPHILS [J].
CARP, H .
JOURNAL OF EXPERIMENTAL MEDICINE, 1982, 155 (01) :264-275
[10]   The NLRP3 inflammasome: A sensor of immune danger signals [J].
Cassel, Suzanne L. ;
Joly, Sophie ;
Sutterwala, Fayyaz S. .
SEMINARS IN IMMUNOLOGY, 2009, 21 (04) :194-198