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    Orphan receptor IL-17RD regulates Toll-like receptor signalling via SEFIR/TIR interactions


    Mellett, Mark, Atzei, Paola, Bergin, Ronan, Horgan, Alan, Floss, Thomas, Wurst, Wolfgang, Callanan, John J. and Moynagh, Paul N. (2015) Orphan receptor IL-17RD regulates Toll-like receptor signalling via SEFIR/TIR interactions. Nature Communications, 6 (6669). ISSN 2041-1723

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    Abstract

    Receptor families of the innate immune response engage in ‘cross-talk’ to tailor optimal immune responses against invading pathogens. However, these responses are subject to multiple levels of regulation to keep in check aberrant inflammatory signals. Here, we describe a role for the orphan receptor interleukin-17 receptor D (IL-17RD) in negatively regulating Toll-like receptor (TLR)-induced responses. Deficiency of IL-17RD expression in cells leads to enhanced pro-inflammatory signalling and gene expression in response to TLR stimulation, and Il17rd−/− mice are more susceptible to TLR-induced septic shock. We demonstrate that the intracellular Sef/IL-17R (SEFIR) domain of IL-17RD targets TIR adaptor proteins to inhibit TLR downstream signalling thus revealing a paradigm involving cross-regulation of members of the IL-17R and TLR families.
    Item Type: Article
    Keywords: Cell signalling; Interleukins; Regulatory networks; Toll-like receptors;
    Academic Unit: Faculty of Science and Engineering > Biology
    Faculty of Science and Engineering > Research Institutes > Institute of Immunology
    Item ID: 11036
    Identification Number: 10.1038/ncomms7669
    Depositing User: Professor Paul Moynagh
    Date Deposited: 16 Sep 2019 13:55
    Journal or Publication Title: Nature Communications
    Publisher: Nature Publshing Group
    Refereed: Yes
    Funders: Immunology Research Centre, Science Foundation Ireland (SFI), Programme for Research in Third Level Institutions (PRTLI) Cycle 5
    Related URLs:
    URI: https://mural.maynoothuniversity.ie/id/eprint/11036
    Use Licence: This item is available under a Creative Commons Attribution Non Commercial Share Alike Licence (CC BY-NC-SA). Details of this licence are available here

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