Extracellular and intracellular decoys in the tuning of inflammatory cytokines and Toll-like receptors: the new entry TIR8/SIGIRR

被引:60
作者
Mantovani, A
Locati, M
Polentarutti, N
Vecchi, A
Garlanda, C
机构
[1] Ist Ric Farmacol Mario Negri, Dept Immunol & Cell Biol, I-20157 Milan, Italy
[2] Univ Milan, Ctr Eccellenza Innovaz Diagnost & Terapeut, Inst Gen Pathol, Fac Med, Milan, Italy
关键词
inflammation; interleukin-1; signaling; chemokines;
D O I
10.1189/jlb.1003473
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Following the identification of the interleukin (IL)-1 type II receptor as a prototypic decoy receptor, nonsignaling receptors with decoy functions have been identified for members of the IL-1/IL-18, tumor necrosis factor, IL-10, and IL-13 receptor families. Moreover, the silent receptor D6 is a promiscuous decoy and scavenger receptor of inflammatory chemokines. The type II IL-1 decoy receptor also acts as a dominant-negative molecule. Intracellular pathways of inhibition of IL-1 and Toll-like receptor (TLR) signaling have been identified. In particular, recent results suggest that the To11/IL-1 receptor (TIR) family member TIR8, also known as single immunoglobulin IL-1-related receptor (SIGIRR), is a negative regulator of IL-1 and TLR signaling. Thus, extracellular and intracellular decoys tune the activation of members of the IL-1/TLR receptor family.
引用
收藏
页码:738 / 742
页数:5
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