| First Author | Sakuma C | Year | 2015 |
| Journal | Mol Immunol | Volume | 63 |
| Issue | 2 | Pages | 328-36 |
| PubMed ID | 25213142 | Mgi Jnum | J:222332 |
| Mgi Id | MGI:5644373 | Doi | 10.1016/j.molimm.2014.08.004 |
| Citation | Sakuma C, et al. (2015) Specific binding of the WASP N-terminal domain to Btk is critical for TLR2 signaling in macrophages. Mol Immunol 63(2):328-36 |
| abstractText | Wiskott-Aldrich syndrome protein (WASP) is an adaptor molecule in immune cells. Recently, we revealed that WASP is involved in lipopolysaccharide-TLR4 signaling in macrophages by association of Bruton's tyrosine kinase (Btk) with the WASP N-terminal domain. Btk has been shown to play important roles in the signaling of several TLRs and to modulate the inflammatory response in macrophages. In this study, we evaluated the importance of the interaction between Btk and WASP in TLR2 signaling by using bone marrow-derived macrophage cell lines from transgenic (Tg) mice expressing anti-WASP N-terminal domain single-chain variable fragment (scFv) or VL single-domain intrabodies. In this Tg bone marrow-derived macrophages, specific interaction between WASP and Btk were strongly inhibited by masking of the binding site in the WASP N-terminal domain. There was impairment of gene expression of TNF-alpha, IL-6, and IL-1beta and phosphorylation of inhibitor of kappaB alpha/beta (IKKalpha/beta) and nuclear factor (NF)-kappaB upon stimulation with TLR2 ligands. Furthermore, tyrosine phosphorylation of WASP following TLR2-ligand stimulation was severely inhibited in the Tg bone marrow-derived macrophages, as shown by the impairment in WASP tyrosine phosphorylation following lipopolysaccharide stimulation. These results strongly suggest that the association between the WASP N-terminal domain and Btk plays an important role in the TLR2-signaling pathway in macrophages. |
