The NLRP3 inflammasome: A sensor of immune danger signals

被引:188
作者
Cassel, Suzanne L. [1 ]
Joly, Sophie [2 ]
Sutterwala, Fayyaz S. [2 ,3 ]
机构
[1] Univ Iowa, Div Allergy & Immunol, Dept Internal Med, Iowa City, IA 52242 USA
[2] Univ Iowa, Inflammat Program, Dept Internal Med, Iowa City, IA 52242 USA
[3] Univ Iowa, Div Infect Dis, Dept Internal Med, Iowa City, IA 52242 USA
基金
美国国家卫生研究院;
关键词
Inflammasome; NLRP3; Caspase-1; Interleukin-1; beta; PATTERN-RECOGNITION RECEPTORS; MUCKLE-WELLS-SYNDROME; NALP3; INFLAMMASOME; INTERLEUKIN-1-BETA RELEASE; DENDRITIC CELLS; URIC-ACID; ACTIVATION; CASPASE-1; INFECTION; SECRETION;
D O I
10.1016/j.smim.2009.05.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The innate immune system senses danger signals via evolutionary conserved receptors. The nucleotide-binding domain leucine-rich repeat containing receptor (NLR) family is a group of intracellular receptors that drive a wide variety of inflammatory responses. A number of the NLR family members can form inflammasomes, which are multiprotein complexes that can activate caspase-1 and ultimately lead to the processing and secretion of interleukin (IL)-1 beta, IL-18 and IL-33. One of the best-studied members of the NLR family is NLRP3 for which a number of divergent activators have recently been described. These and other studies examining the NLRP3 inflammasome will be discussed in this review. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:194 / 198
页数:5
相关论文
共 54 条
[1]   NALP3 forms an IL-lβ-Processing inflammasome with increased activity in Muckle-Wells autoinflammatory disorder [J].
Agostini, L ;
Martinon, F ;
Burns, K ;
McDermott, MF ;
Hawkins, PN ;
Tschopp, J .
IMMUNITY, 2004, 20 (03) :319-325
[2]   Pattern recognition receptors: From the cell surface to intracellular dynamics [J].
Altenbach, Denise ;
Robatzek, Silke .
MOLECULAR PLANT-MICROBE INTERACTIONS, 2007, 20 (09) :1031-1039
[3]   Nalp1b controls mouse macrophage susceptibility to anthrax lethal toxin [J].
Boyden, ED ;
Dietrich, WF .
NATURE GENETICS, 2006, 38 (02) :240-244
[4]   The Nalp3 inflammasome is essential for the development of silicosis [J].
Cassel, Suzanne L. ;
Eisenbarth, Stephanie C. ;
Iyer, Shankar S. ;
Sadler, Jeffrey J. ;
Colegio, Oscar R. ;
Tephly, Linda A. ;
Carter, A. Brent ;
Rothman, Paul B. ;
Flavell, Richard A. ;
Sutterwala, Fayyaz S. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (26) :9035-9040
[5]   ATP activates a reactive oxygen species-dependent oxidative stress response and secretion of proinflammatory cytokines in macrophages [J].
Cruz, Cristiane M. ;
Rinna, Alessandra ;
Forman, Henry Jay ;
Ventura, Ana L. M. ;
Persechini, Pedro M. ;
Ojcius, David M. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (05) :2871-2879
[6]   New mutations of CIAS1 that are responsible for Muckle-Wells syndrome and familial cold urticaria:: A novel mutation underlies both syndromes [J].
Dodé, C ;
Le Dû, N ;
Cuisset, L ;
Letourneur, F ;
Berthelot, JM ;
Vaudour, G ;
Meyrier, A ;
Watts, RA ;
Scott, DGI ;
Nicholls, A ;
Granel, B ;
Frances, C ;
Garcier, F ;
Edery, P ;
Boulinguez, S ;
Domergues, JP ;
Delpech, M ;
Grateau, G .
AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 70 (06) :1498-1506
[7]   Intracellular pattern-recognition receptors [J].
Dostert, Catherine ;
Meylan, Etienne ;
Tschopp, Juerg .
ADVANCED DRUG DELIVERY REVIEWS, 2008, 60 (07) :830-840
[8]   Innate immune activation through Nalp3 inflammasome sensing of asbestos and silica [J].
Dostert, Catherine ;
Petrilli, Virginie ;
Van Bruggen, Robin ;
Steele, Chad ;
Mossman, Brooke T. ;
Tschopp, Jurg .
SCIENCE, 2008, 320 (5876) :674-677
[9]   Crucial role for the Nalp3 inflammasome in the immunostimulatory properties of aluminium adjuvants [J].
Eisenbarth, Stephanie C. ;
Colegio, Oscar R. ;
O'Connor, William, Jr. ;
Sutterwala, Fayyaz S. ;
Flavell, Richard A. .
NATURE, 2008, 453 (7198) :1122-U13
[10]   Chronic infantile neurological cutaneous and articular syndrome is caused by mutations in CIAS1, a gene highly expressed in polymorphonuclear cells and chondrocytes [J].
Feldmann, J ;
Prieur, AM ;
Quartier, P ;
Berquin, P ;
Certain, S ;
Cortis, E ;
Teillac-Hamel, D ;
Fischer, A ;
de Saint Basile, G .
AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (01) :198-203