Proteolytic Processing of Interleukin-1 Family Cytokines: Variations on a Common Theme

被引:386
作者
Afonina, Inna S. [1 ,2 ]
Muller, Christina [1 ,2 ]
Martin, Seamus J. [3 ]
Beyaert, Rudi [1 ,2 ]
机构
[1] VIB, Inflammat Res Ctr, Unit Mol Signal Transduct Inflammat, B-9052 Ghent, Belgium
[2] Univ Ghent, Dept Biomed Mol Biol, B-9052 Ghent, Belgium
[3] Trinity Coll Dublin, Smurfit Inst, Dept Genet, Mol Cell Biol Lab, Dublin 2, Ireland
关键词
MAST-CELL CHYMASE; GENERALIZED PUSTULAR PSORIASIS; ALLERGIC AIRWAY INFLAMMATION; GAMMA-INDUCING FACTOR; GRANZYME-B; CONVERTING-ENZYME; STERILE INFLAMMATION; HUMAN KERATINOCYTES; MICE DEFICIENT; IN-VIVO;
D O I
10.1016/j.immuni.2015.06.003
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Members of the extended interleukin-1 (IL-1) cytokine family, such as IL-1, IL-18, IL-33, and IL-36, play a pivotal role in the initiation and amplification of immune responses. However, deregulated production and/or activation of these cytokines can lead to the development of multiple inflammatory disorders. IL-1 family members share a broadly similar domain organization and receptor signaling pathways. Another striking similarity between IL-1 family members is the requirement for proteolytic processing in order to unlock their full biological potential. Although much emphasis has been put on the role of caspase-1, another emerging theme is the involvement of neutrophil-and mast cell-derived proteases in IL-1 family cytokine processing. Elucidating the regulation of IL-1 family members by proteolytic processing is of great interest for understanding inflammation and immunity. Here, we review the identity of the proteases involved in the proteolytic processing of IL-1 family cytokines and the therapeutic implications in inflammatory disease.
引用
收藏
页码:991 / 1004
页数:14
相关论文
共 118 条
[101]   The IL-1 family member 7b translocates to the nucleus and down-regulates proinflammatory cytokines [J].
Sharma, Sheetal ;
Kulk, Nicole ;
Nold, Marcel F. ;
Graef, Ralph ;
Kim, Soo-Hyun ;
Reinhardt, Dietrich ;
Dinarello, Charles A. ;
Bufler, Philip .
JOURNAL OF IMMUNOLOGY, 2008, 180 (08) :5477-5482
[102]   Cutting Edge: Endoplasmic Reticulum Stress Licenses Macrophages To Produce Mature IL-1β in Response to TLR4 Stimulation through a Caspase-8-and TRIF-Dependent Pathway [J].
Shenderov, Kevin ;
Riteau, Nicolas ;
Yip, Ronald ;
Mayer-Barber, Katrin D. ;
Oland, Sandy ;
Hieny, Sara ;
Fitzgerald, Pat ;
Oberst, Andrew ;
Dillon, Christopher P. ;
Green, Douglas R. ;
Cerundolo, Vincenzo ;
Sher, Alan .
JOURNAL OF IMMUNOLOGY, 2014, 192 (05) :2029-2033
[103]   Four new members expand the interleukin-1 superfamily [J].
Smith, DE ;
Renshaw, BR ;
Ketchem, RR ;
Kubin, M ;
Garka, KE ;
Sims, JE .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (02) :1169-1175
[104]   Neutrophil proteinase 3-mediated induction of bioactive IL-18 secretion by human oral epithelial cells [J].
Sugawara, S ;
Uehara, A ;
Nochi, T ;
Yamaguchi, T ;
Ueda, H ;
Sugiyama, A ;
Hanzawa, K ;
Kumagai, K ;
Okamura, H ;
Takada, H .
JOURNAL OF IMMUNOLOGY, 2001, 167 (11) :6568-6575
[105]   Generalized Pustular Psoriasis Triggered by Amoxicillin in Monozygotic Twins with Compound Heterozygous IL36RN Mutations: Comment on the Article by Navarini et al. [J].
Sugiura, Kazumitsu ;
Shoda, Yukiko ;
Akiyama, Masashi .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2014, 134 (02) :578-579
[106]   Interleukin-33 Is Biologically Active Independently of Caspase-1 Cleavage [J].
Talabot-Ayer, Dominique ;
Lamacchia, Celine ;
Gabay, Cem ;
Palmer, Gaby .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2009, 284 (29) :19420-19426
[107]   A NOVEL HETERODIMERIC CYSTEINE PROTEASE IS REQUIRED FOR INTERLEUKIN-1-BETA PROCESSING IN MONOCYTES [J].
THORNBERRY, NA ;
BULL, HG ;
CALAYCAY, JR ;
CHAPMAN, KT ;
HOWARD, AD ;
KOSTURA, MJ ;
MILLER, DK ;
MOLINEAUX, SM ;
WEIDNER, JR ;
AUNINS, J ;
ELLISTON, KO ;
AYALA, JM ;
CASANO, FJ ;
CHIN, J ;
DING, GJF ;
EGGER, LA ;
GAFFNEY, EP ;
LIMJUCO, G ;
PALYHA, OC ;
RAJU, SM ;
ROLANDO, AM ;
SALLEY, JP ;
YAMIN, TT ;
LEE, TD ;
SHIVELY, JE ;
MACCROSS, M ;
MUMFORD, RA ;
SCHMIDT, JA ;
TOCCI, MJ .
NATURE, 1992, 356 (6372) :768-774
[108]   Interleukin-36 (IL-36) Ligands Require Processing for Full Agonist (IL-36α, IL-36β, and IL-36γ) or Antagonist (IL-36Ra) Activity [J].
Towne, Jennifer E. ;
Renshaw, Blair R. ;
Douangpanya, Jason ;
Lipsky, Brian P. ;
Shen, Min ;
Gabel, Christopher A. ;
Sims, John E. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2011, 286 (49) :42594-42602
[109]   Caspase-1-independent, Fas/Fas ligand-mediated IL-18 secretion from macrophages causes acute liver injury in mice [J].
Tsutsui, H ;
Kayagaki, N ;
Kuida, K ;
Nakano, H ;
Hayashi, N ;
Takeda, K ;
Matsui, K ;
Kashiwamura, S ;
Hada, T ;
Akira, S ;
Yagita, H ;
Okamura, H ;
Nakanishi, K .
IMMUNITY, 1999, 11 (03) :359-367
[110]  
Ushio S, 1996, J IMMUNOL, V156, P4274