Mature interleukin-33 is produced by calpain-mediated cleavage in vivo

被引:72
作者
Hayakawa, Morisada [1 ]
Hayakawa, Hiroko [1 ]
Matsuyama, Yasushi [2 ]
Tamemoto, Hiroyuki [1 ]
Okazaki, Hitoaki [2 ]
Tominaga, Shin-ichi [1 ]
机构
[1] Jichi Med Univ, Dept Biochem, Shimotsuke, Tochigi 3290498, Japan
[2] Jichi Med Univ, Div Clin Immunol & Rheumatol, Shimotsuke, Tochigi 3290498, Japan
关键词
IL-33; IL-1; family; ST2; Processing; Calpain; IL-1-LIKE CYTOKINE IL-33; CONVERTING-ENZYME; RECEPTOR; ST2; PRECURSOR; PROTEASE; IDENTIFICATION; TRANSCRIPTION; ACTIVATION; EXPRESSION;
D O I
10.1016/j.bbrc.2009.07.018
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
Interleukin (IL)-33 is a novel member of the IL-1 family. IL-33 is primarily synthesized as a 30-kDa precursor (pro-IL-33). Pro-IL-33 is cleaved by caspase-1 into an 18-kDa mature form (mature IL-33) in vitro. Recombinant mature IL-33 has been known to induce T-helper type-2 (Th2)-associated cytokines and inflammatory cytokines via its receptor, ST2L However, processing of pro-IL-33 in vivo has not been clarified yet. Here, we report that calpain mediates pro-IL-33 processing in vivo. Pro-IL-33 was expressed by stimulating human epithelial cells with phorbol 12-myristate 13-acetate. Calcium ionophore induced pro-IL-33 cleavage and mature IL-33 production. This cleavage was inhibited by treatment with a calcium and calpain inhibitors. Moreover, short interfering RNA-mediated knockdown of calpains chelator suppressed pro-IL-33 cleavage. These results indicate that calpains play a critical role in pro-IL-33 processing in vivo. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:218 / 222
页数:5
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