Cutting Edge: Evidence for Ligand-Independent Multimerization of the IL-17 Receptor
Author(s) -
Jill M. Kramer,
Ling Yi,
Fang Shen,
Amarnath Maitra,
Xuanmao Jiao,
Tian Jin,
Sarah L. Gaffen
Publication year - 2006
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.176.2.711
Subject(s) - förster resonance energy transfer , receptor , protein subunit , cytokine receptor , ligand (biochemistry) , hek 293 cells , cyan , biophysics , biology , chemistry , cytokine , microbiology and biotechnology , biochemistry , fluorescence , immunology , gene , art , physics , quantum mechanics , visual arts
IL-17 and its receptor are founding members of a novel inflammatory cytokine family. To date, only one IL-17 receptor subunit has been identified, termed IL-17RA. All known cytokine receptors consist of a complex of multiple subunits. Although IL-17-family cytokines exist as homodimers, the configuration and stoichiometry of the IL-17R complex remain unknown. We used fluorescence resonance energy transfer (FRET) to determine whether IL-17RA subunits multimerize, and, if so, whether they are preassembled in the plasma membrane. HEK293 cells coexpressing IL-17RA fused to cyan or yellow fluorescent proteins (CFP or YFP) were used to evaluate FRET before and after IL-17A or IL-17F treatment. In the absence of ligand, IL-17RA molecules exhibited significant specific FRET efficiency, demonstrating that they exist in a multimeric, preformed receptor complex. Strikingly, treatment with IL-17A or IL-17F markedly reduced FRET efficiency, suggesting that IL-17RA subunits within the IL-17R complex undergo a conformational change upon ligand binding.
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