MDP-induced interleukin-1β processing requires Nod2 and CIAS1/NALP3

被引:112
作者
Pan, Qilin
Mathison, John
Fearns, Colleen
Kravchenko, Vladimir V.
Correia, Jean Da Silva
Hoffman, Hal M.
Kobayashi, Koichi S.
Bertin, John
Grant, Ethan P.
Coyle, Anthony J.
Sutterwala, Fayyaz S.
Ogura, Yasunori
Flavell, Richard A.
Ulevitch, Richard J.
机构
[1] Scripps Res Inst, Dept Immunol, La Jolla, CA 92037 USA
[2] Univ Calif San Diego, La Jolla, CA 92093 USA
[3] Ludwig Inst Canc Res, La Jolla, CA USA
[4] Harvard Univ, Sch Publ Hlth, Dana Farber Canc Inst, Dept Canc Immunol & AIDS, Boston, MA 02115 USA
[5] Millennium Pharmaceut Inc, Cambridge, MA USA
[6] Yale Univ, Sch Med, Immunobiol Sect, New Haven, CT USA
关键词
cytokine; inflammation; PAMP; NLR;
D O I
10.1189/jlb.1006627
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Nucleotide-binding oligomerization domain (Nod)2 is a sensor of muramyl dipeptides (AIDP) derived from bacterial peptidoglycan. Nod2 also plays a role in some autoinflammatory diseases. Cold-induced autoinflammatory syndrome I (CIAS1)/NACHT domain, leucine-rich repeat, and pyrin domain-containing protein 3 (NALP3) has been suggested to be sufficient for MDP-dependent release of mature IL-1 beta, but the role of Nod2 in this process is unclear. Using mice bearing selective gene deletions, we provide in vitro and in vivo data showing that AIDP-induced IL-1 beta release requires Nod2 and CIASI/NALP3 as well as receptor-interacting protein-2 (Rip2), apoptosis-associated speck-like protein containing a caspase activation and recruitment domain (ASC), and caspase-1. In contrast, AIDP-dependent IL-6 production only requires Nod2 and Rip2. Together, our data provide a new understanding of this important pathway of IL-I beta production and allow for further studies of the role of these proteins within the broader context of inflammatory disease.
引用
收藏
页码:177 / 183
页数:7
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