Innate Immune Receptors as Competitive Determinants of Cell Fate

被引:50
作者
Franz, Kate M. [1 ,2 ]
Kagan, Jonathan C. [1 ,2 ]
机构
[1] Harvard Med Sch, Boston Childrens Hosp, Div Gastroenterol, Boston, MA 02115 USA
[2] Harvard Med Sch, Program Virol, Boston, MA 02115 USA
关键词
DOUBLE-STRANDED-RNA; NONCANONICAL INFLAMMASOME ACTIVATION; PROTEIN-KINASE PKR; CYCLIC GMP-AMP; PATTERN-RECOGNITION; DENDRITIC CELL; RIG-I; TRANSCRIPTION FACTOR; BACTERIAL LIGANDS; ADAPTIVE IMMUNITY;
D O I
10.1016/j.molcel.2017.05.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Infections can cause a multitude of stresses on the host and microbe. To detect potential infections, the mammalian immune system utilizes several families of pattern recognition receptors, which survey the intracellular and extracellular environments for microbial products. Members of each receptor family induce antimicrobial effector responses, which include inflammatory cytokine or interferon expression, downregulation of protein synthesis, or host cell death. In this review, we discuss the benefits of each of these innate immune responses. We highlight hownon-infectious bacteria and viruses typically activate a single family of receptors, which results in a predictable host response. Infections with virulent pathogens, in contrast, may activate receptors from distinct families. As each receptor family may induce responses that antagonize or synergize with the activities of another family, cell fate decisions during pathogenic encounters are unpredictable. Understanding the antagonistic antimicrobial activities of the innate immune system should provide insight into how cell fate decisions are made during infections and potentially during other environmental stresses.
引用
收藏
页码:750 / 760
页数:11
相关论文
共 100 条
[1]   Regulation by destruction: design of the σE envelope stress response [J].
Ades, Sarah E. .
CURRENT OPINION IN MICROBIOLOGY, 2008, 11 (06) :535-540
[2]   Characterization of a mammalian homolog of the GCN2 eukaryotic initiation factor 2α kinase [J].
Berlanga, JJ ;
Santoyo, J ;
de Haro, C .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1999, 265 (02) :754-762
[3]   The role of oxidized phospholipids in atherosclerosis [J].
Berliner, Judith A. ;
Leitinger, Norbert ;
Tsimikas, Sotirios .
JOURNAL OF LIPID RESEARCH, 2009, 50 :S207-S212
[4]   Beyond pattern recognition: five immune checkpoints for scaling the microbial threat [J].
Blander, J. Magarian ;
Sander, Leif E. .
NATURE REVIEWS IMMUNOLOGY, 2012, 12 (03) :215-225
[5]   Toll-dependent selection of microbial antigens for presentation by dendritic cells [J].
Blander, JM ;
Medzhitov, R .
NATURE, 2006, 440 (7085) :808-812
[6]   Protective role of phospholipid oxidation products in endotoxin-induced tissue damage [J].
Bochkov, VN ;
Kadl, A ;
Huber, J ;
Gruber, F ;
Binder, BR ;
Leitinger, N .
NATURE, 2002, 419 (6902) :77-81
[7]   Innate Immune Pattern Recognition: A Cell Biological Perspective [J].
Brubaker, Sky W. ;
Bonham, Kevin S. ;
Zanoni, Ivan ;
Kagan, Jonathan C. .
ANNUAL REVIEW OF IMMUNOLOGY VOL 33, 2015, 33 :257-290
[8]   Recognition and delivery of effector proteins into eukaryotic cells by bacterial secretion systems [J].
Cambronne, Eric D. ;
Roy, Craig R. .
TRAFFIC, 2006, 7 (08) :929-939
[9]   REGULATION OF PROTEIN-SYNTHESIS BY HEME-REGULATED EIF-2-ALPHA KINASE [J].
CHEN, JJ ;
LONDON, IM .
TRENDS IN BIOCHEMICAL SCIENCES, 1995, 20 (03) :105-108
[10]   Dendritic cell maturation triggers retrograde MHC class II transport from lysosomes to the plasma membrane [J].
Chow, A ;
Toomre, D ;
Garrett, W ;
Mellman, I .
NATURE, 2002, 418 (6901) :988-994