Dissecting negative regulation of Toll-like receptor signaling

被引:354
作者
Kondo, Takeshi [1 ,2 ]
Kawai, Taro [1 ,2 ]
Akira, Shizuo [1 ,2 ]
机构
[1] Osaka Univ, Lab Host Def, WPI Immunol Frontier Res Ctr, Suita, Osaka 5650871, Japan
[2] Osaka Univ, Microbial Dis Res Inst, Suita, Osaka 5650871, Japan
基金
美国国家卫生研究院;
关键词
NF-KAPPA-B; ARYL-HYDROCARBON RECEPTOR; I INTERFERON; DC-SIGN; ANTIVIRAL RESPONSE; IMMUNE-RESPONSES; INNATE IMMUNITY; PROTEIN; INFLAMMATION; DEGRADATION;
D O I
10.1016/j.it.2012.05.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Toll-like receptors (TLRs) sense invading microbial pathogens and play crucial roles in the activation of innate and adaptive immunity. However, excessive TLR activation can disrupt immune homeostasis, and may be responsible for the development of autoimmune and inflammatory diseases. As such, the molecules and pathways that negatively control TLR signaling have been intensively investigated. Here, we discuss recent insights into the negative regulation of TLR signaling, with focus on three major mechanisms: (i) dissociation of adaptor complexes; (ii) degradation of signal proteins; and WO transcriptional regulation. We also highlight how pathogens negatively target TLR signaling as a strategy to evade the host immune response.
引用
收藏
页码:449 / 458
页数:10
相关论文
共 97 条
[1]   Leishmania-Induced IRAK-1 Inactivation Is Mediated by SHP-1 Interacting with an Evolutionarily Conserved KTIM Motif [J].
Abu-Dayyeh, Issa ;
Shio, Marina Tiemi ;
Sato, Shintaro ;
Akira, Shizuo ;
Cousineau, Benoit ;
Olivier, Martin .
PLOS NEGLECTED TROPICAL DISEASES, 2008, 2 (12)
[2]   TAK1 Negatively Regulates NF-κB and p38 MAP Kinase Activation in Gr-1+CD11b+ Neutrophils [J].
Ajibade, Adebusola Alagbala ;
Wang, Qinfu ;
Cui, Jun ;
Zou, Jia ;
Xia, Xiaojun ;
Wang, Mingjun ;
Tong, Yanzheng ;
Hui, Wei ;
Liu, Dou ;
Su, Bing ;
Wang, Helen Y. ;
Wang, Rong-Fu .
IMMUNITY, 2012, 36 (01) :43-54
[3]   Pathogen recognition and innate immunity [J].
Akira, S ;
Uematsu, S ;
Takeuchi, O .
CELL, 2006, 124 (04) :783-801
[4]   Phosphatase SHP-1 promotes TLR- and RIG-I-activated production of type I interferon by inhibiting the kinase IRAK1 [J].
An, Huazhang ;
Hou, Jin ;
Zhou, Jun ;
Zhao, Wei ;
Xu, Hongmei ;
Zheng, Yuejuan ;
Yu, Yizhi ;
Liu, Shuxun ;
Cao, Xuetao .
NATURE IMMUNOLOGY, 2008, 9 (05) :542-550
[5]   SHP-2 phosphatase negatively regulates the TRIF adaptor protein-dependent type I interferon and proinflammatory cytokine production [J].
An, Huazhang ;
Zhao, Wei ;
Hou, Jin ;
Zhang, Yan ;
Xie, Yun ;
Zheng, Yuejuan ;
Xu, Hongmei ;
Qian, Cheng ;
Zhou, Jun ;
Yu, Yizhi ;
Liu, Shuxun ;
Feng, Gensheng ;
Cao, Xuetao .
IMMUNITY, 2006, 25 (06) :919-928
[6]   The kinases MSK1 and MSK2 act as negative regulators of Toll-like receptor signaling [J].
Ananieva, Olga ;
Darragh, Joanne ;
Johansen, Claus ;
Carr, Julia M. ;
McIlrath, Joanne ;
Park, Jin Mo ;
Wingate, Andrew ;
Monk, Claire E. ;
Toth, Rachel ;
Santos, Susana G. ;
Iversen, Lars ;
Arthur, J. Simon C. .
NATURE IMMUNOLOGY, 2008, 9 (09) :1028-1036
[7]   A bacterial E3 ubiquitin ligase IpaH9.8 targets NEMO/IKKγ to dampen the host NF-κB-mediated inflammatory response [J].
Ashida, Hiroshi ;
Kim, Minsoo ;
Schmidt-Supprian, Marc ;
Ma, Averil ;
Ogawa, Michinaga ;
Sasakawa, Chihiro .
NATURE CELL BIOLOGY, 2010, 12 (01) :66-U164
[8]   Nucleic acids of mammalian origin can act as endogenous ligands for toll-like receptors and may promote systemic lupus erythematosus [J].
Barrat, FJ ;
Meeker, T ;
Gregorio, J ;
Chan, JH ;
Uematsu, S ;
Akira, S ;
Chang, B ;
Duramad, O ;
Coffman, RL .
JOURNAL OF EXPERIMENTAL MEDICINE, 2005, 202 (08) :1131-1139
[9]   Treatment of lupus-prone of TLR7 and TLR9 leads to mice with a dual inhibitor reduction of autoantibody production and amelioration of disease symptoms [J].
Barrat, Franck J. ;
Meeker, Thea ;
Chan, Jean H. ;
Guiducci, Cristiana ;
Cofftnan, Robert L. .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2007, 37 (12) :3582-3586
[10]  
Barry Michele, 2006, Sci STKE, V2006, ppe21