C4b-binding protein negatively regulates TLR4/MD-2 response but not TLR3 response

被引:5
作者
Morita, Naoko [1 ]
Yamazaki, Tatsuya [1 ]
Murakami, Yusuke [2 ]
Fukui, Ryutaro [2 ]
Yamai, Ikuko [2 ]
Ichimonji, Isao [1 ]
Nakashima, Akina [1 ]
Nagaoka, Fumiaki [1 ]
Takagi, Hidekazu [1 ]
Miyake, Kensuke [2 ]
Akashi-Takamura, Sachiko [1 ]
机构
[1] Aichi Med Univ, Sch Med, Dept Microbiol & Immunol, 1-1 Yazakokarimata, Nagakute, Aichi 4801195, Japan
[2] Univ Tokyo, Inst Med Sci, Dept Microbiol & Immunol, Div Innate Immun, Tokyo, Japan
关键词
C4b-binding protein; lipopolysaccharide; toll-like receptor; TOLL-LIKE RECEPTORS; SURFACE; CELLS; RECOGNITION; EXPRESSION; IMMUNITY; BINDING; PRAT4A; ROLES; MD-2;
D O I
10.1002/1873-3468.12693
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
Recently, we reported a novel function for C4b-binding protein (C4BP) in inhibiting the toll-like receptor (TLR)1/2 response by interacting with TLR2-TLRs share a common structure; hence, we examined the effect of C4BP on activation of other TLRs/TLR4 and TLR3. The results of immunoprecipitation assays suggest that C4BP interacts with TLR4/MD-2 but not TLR3-C4BP inhibits TLR4/MD-2-mediated, but not TLR3-mediated, proinflammatory cytokine production and nuclear factor (NF)-kappa B signaling. C4BP-deficient mice show increased interleukin (IL)-6 production in response to the TLR4/MD-2 ligand. A competition assay revealed that C4BP prevents an interaction between TLR4/MD-2 and its ligand. These findings indicate that C4BP binds to cell surface TLRs and inhibits the TLR-TLR ligand interaction, thereby inhibiting TLR activation.
引用
收藏
页码:1732 / 1741
页数:10
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