Cutting edge: Role of Toll-like receptor 1 in mediating immune response to microbial lipoproteins

被引:1026
作者
Takeuchi, O
Sato, S
Horiuchi, T
Hoshino, K
Takeda, K
Dong, ZY
Modlin, RL
Akira, S
机构
[1] Osaka Univ, Dept Host Def, Microbial Dis Res Inst, Suita, Osaka 5650871, Japan
[2] Japan Sci & Technol Corp, Solut Oriented Res Sci & Technol, Osaka, Japan
[3] Univ Texas, Dept Canc Biol, MD Anderson Canc Ctr, Houston, TX 77030 USA
[4] Univ Calif Los Angeles, Sch Med, Div Dermatol, Dept Microbiol & Immunol, Los Angeles, CA 90095 USA
[5] Univ Calif Los Angeles, Sch Med, Inst Mol Biol, Los Angeles, CA 90095 USA
关键词
D O I
10.4049/jimmunol.169.1.10
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 Toll-like receptor (TLR) family acts as pattern recognition receptors for pathogen-specific molecular patterns (PAMPs). TLR2 is essential for the signaling of a variety of PAMPs, including bacterial lipoprotein/lipopeptides, peptidoglycan, and GPI anchors. TLR6 associates with TLR2 and recognizes diacylated mycoplasmal lipopeptide along with TLR2. We report here that TLR1 associates with TLR2 and recognizes the native mycobacterial 19-kDa lipoprotein along with TLR2. Macrophages from TLR1-deficient (TLR1(-/-)) mice showed impaired proinflammatory cytokine production in response to the 19-kDa lipoprotein and a synthetic triacylated lipopeptide. In contrast, TLR1(-/-) cells responded normally to diacylated lipopeptide. TLR1 interacts with TLR2 and coexpression of TLR1 and TLR2 enhanced the NF-kappaB activation in response to a synthetic lipopeptide. Furthermore, lipoprotein analogs whose acylation was modified were preferentially recognized by TLR1. Taken together, TLR1 interacts with TLR2 to recognize the lipid configuration of the native mycobacterial lipoprotein as well as several triacylated lipopeptides.
引用
收藏
页码:10 / 14
页数:5
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