Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10770978 | Biochemical and Biophysical Research Communications | 2005 | 4 Pages |
Abstract
CD14 has been shown to enhance Toll-like receptor 2 (TLR2)-mediated signaling in response to peptidoglycan. Anti-CD14 monoclonal antibody MEM-18, whose epitope was located at the amino acid residues 57-64, blocked the binding of sCD14 to the recombinant soluble form of the extracellular TLR2 domain (sTLR2). The deletion mutant sCD14Î57-64 lacking the amino acid residues 57-64 failed to bind to sTLR2. Cotransfection of wild type mCD14 but not mCD14Î57-64 with TLR2 enhanced NF-κB activation in response to peptidoglycan. These results indicate that the CD14 region spanning amino acids 57-64 is critical for interacting with TLR2 and enhancing TLR2-mediated peptidoglycan signaling.
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Authors
Daisuke Iwaki, Chiaki Nishitani, Hiroaki Mitsuzawa, Naoki Hyakushima, Hitomi Sano, Yoshio Kuroki,