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Publication : Flightless I homolog negatively modulates the TLR pathway.

First Author  Wang T Year  2006
Journal  J Immunol Volume  176
Issue  3 Pages  1355-62
PubMed ID  16424162 Mgi Jnum  J:126432
Mgi Id  MGI:3761242 Doi  10.4049/jimmunol.176.3.1355
Citation  Wang T, et al. (2006) Flightless I homolog negatively modulates the TLR pathway. J Immunol 176(3):1355-62
abstractText  To date, much of our knowledge about the signaling networks involved in the innate immune response has come from studies using nonphysiologic model systems rather than actual immune cells. In this study, we used a dual-tagging proteomic strategy to identify the components of the MyD88 signalosome in murine macrophages stimulated with lipid A. This systems approach revealed 16 potential MyD88-interacting partners, one of which, flightless I homolog (Fliih) was verified to interact with MyD88 and was further characterized as a negative regulator of the TLR4-MyD88 pathway. Conversely, a reduction in endogenous Fliih by small-interfering RNA enhanced the activation of NF-kappaB, as well as cytokine production by LPS. Results from immunoprecipitation and a two-hybrid assay further indicated that Fliih directly interfered with the formation of the TLR4-MyD88 signaling complex. These results in turn suggest a new basis for the regulation of the TLR pathway by Fliih.
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