The Signaling Pathways Regulating NLRP3 Inflammasome Activation

被引:113
作者
Chen, Ming-ye [1 ]
Ye, Xun-jia [1 ]
He, Xian-hui [1 ]
Ouyang, Dong-yun [1 ]
机构
[1] Jinan Univ, Coll Life Sci & Technol, Dept Immunobiol, Guangzhou 510632, Peoples R China
基金
中国国家自然科学基金;
关键词
NLRP3; inflammasome; mTOR; MAPK; Autophagy; PKA; AMPK; FACTOR-KAPPA-B; PROTEIN-KINASE; OXIDATIVE STRESS; INTERLEUKIN-1; PRODUCTION; CASPASE-11; ACTIVATION; TRANSCRIPTION FACTORS; LYSOSOME RUPTURE; INNATE IMMUNITY; CYCLIC-AMP; K+ EFFLUX;
D O I
10.1007/s10753-021-01439-6
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The NLRP3 inflammasome is a multi-molecular complex that acts as a molecular platform to mediate caspase-1 activation, leading to IL-1 beta/IL-18 maturation and release in cells stimulated by various pathogen-associated molecular patterns (PAMPs) or damageassociated molecular patterns (DAMPs). This inflammasome plays an important role in the innate immunity as its activation can further promote the occurrence of inflammation, enhance the ability of host to remove pathogens, and thus facilitate the repair of injured tissues. But if the inflammasome activation is dysregulated, it will cause the development of various inflammatory diseases and metabolic disorders. Therefore, under normal conditions, the activation of inflammasome is tightly regulated by various positive and negative signaling pathways to respond to the stimuli without damaging the host itself while maintaining homeostasis. In this review, we summarize recent advances in the major signaling pathways (including TLRs, MAPK, mTOR, autophagy, PKA, AMPK, and IFNR) that regulate NLRP3 inflammasome activation, providing a brief view of the molecular network that regulates this inflammasome as a theoretical basis for therapeutic intervention of NLRP3 dysregulationrelated diseases.
引用
收藏
页码:1229 / 1245
页数:17
相关论文
共 150 条
[1]   Defective noncanonical autophagy in SLE-like disease [J].
Susan J. Allison .
Nature Reviews Nephrology, 2016, 12 (7) :375-375
[2]   Mitogen-activated protein kinases in innate immunity [J].
Arthur, J. Simon C. ;
Ley, Steven C. .
NATURE REVIEWS IMMUNOLOGY, 2013, 13 (09) :679-692
[3]   The eIF2α/ATF4 pathway is essential for stress-induced autophagy gene expression [J].
B'chir, Wafa ;
Maurin, Anne-Catherine ;
Carraro, Valerie ;
Averous, Julien ;
Jousse, Celine ;
Muranishi, Yuki ;
Parry, Laurent ;
Stepien, Georges ;
Fafournoux, Pierre ;
Bruhat, Alain .
NUCLEIC ACIDS RESEARCH, 2013, 41 (16) :7683-7699
[4]   Caspase-1 self-cleavage is an intrinsic mechanism to terminate inflammasome activity [J].
Boucher, Dave ;
Monteleone, Mercedes ;
Coll, Rebecca C. ;
Chen, Kaiwen W. ;
Ross, Connie M. ;
Teo, Jessica L. ;
Gomez, Guillermo A. ;
Holley, Caroline L. ;
Bierschenk, Damien ;
Stacey, Katryn J. ;
Yap, Alpha S. ;
Bezbradica, Jelena S. ;
Schroder, Kate .
JOURNAL OF EXPERIMENTAL MEDICINE, 2018, 215 (03) :827-840
[5]  
BRANDWEIN SR, 1986, J BIOL CHEM, V261, P8624
[6]   Interaction between autophagy and the NLRP3 inflammasome [J].
Cao, Zhenrui ;
Wang, Yanhao ;
Long, Zhimin ;
He, Guiqiong .
ACTA BIOCHIMICA ET BIOPHYSICA SINICA, 2019, 51 (11) :1087-1095
[7]   Inflammasome signaling and regulation of interleukin-1 family cytokines [J].
Chan, Amy H. ;
Schroder, Kate .
JOURNAL OF EXPERIMENTAL MEDICINE, 2020, 217 (01)
[8]   Mammalian MAP kinase signalling cascades [J].
Chang, LF ;
Karin, M .
NATURE, 2001, 410 (6824) :37-40
[9]   Peptidoglycan-induced IL-6 production in RAW 264.7 macrophages is mediated by cyclooxygenase-2, PGE2/PGE4 receptors, protein kinase A, IκB kinase, and NF-KB1 [J].
Chen, BC ;
Liao, CC ;
Hsu, MJ ;
Liao, YT ;
Lin, CC ;
Sheu, JR ;
Lin, CH .
JOURNAL OF IMMUNOLOGY, 2006, 177 (01) :681-693
[10]   PtdIns4P on dispersed trans-Golgi network mediates NLRP3 inflammasome activation [J].
Chen, Jueqi ;
Chen, Zhijian J. .
NATURE, 2018, 564 (7734) :71-+