Cutting edge: Naturally occurring soluble form of mouse toll-like receptor 4 inhibits lipopolysaccharide signaling

被引:230
作者
Iwami, K
Matsuguchi, T
Masuda, A
Kikuchi, T
Musikacharoen, T
Yoshikai, Y
机构
[1] Nagoya Univ, Sch Med, Lab Host Def & Germfree Life, Dis Mechanism & Control Res Inst,Showa Ku, Nagoya, Aichi 4668550, Japan
[2] Aichi Gakuin Univ, Sch Dent, Dept Periodontol, Nagoya, Aichi 464, Japan
关键词
D O I
10.4049/jimmunol.165.12.6682
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Toll-like receptors (TLRs) are a family of proteins playing important roles in host defense. Mice defective of functional TLR4 are hyporesponsive to LPS, suggesting that TLR4 is essential for LPS signaling. Here we report the cloning of an alternatively spliced mouse TLR4 (mTLR4) mRNA, The additional exon exists between the second and third exon of the reported mTLR4 gene and contains an in-frame stop codon, The alternatively spliced mRNA encodes 86 aa of the reported mTLR4 and an additional 36 aa, This alternatively spliced mTLR4 mRNA expressed a partially secretary 20-kDa protein, which we named soluble mTLR4 (smTLR4), In a mouse macrophage cell line, the exogenously expressed smTLR4 significantly inhibited LPS-mediated TNF-alpha production and NF-KB activation. Additionally, in mouse macrophages, LPS increased the mRNA for smTLR4, Taken together, our results indicate that smTLR4 may function as a feedback mechanism to inhibit the excessive LPS responses in mouse macrophages.
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收藏
页码:6682 / 6686
页数:5
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