| Literature DB >> 17355969 |
Jill F Wright1, Yongjing Guo, Amira Quazi, Deborah P Luxenberg, Frann Bennett, John F Ross, Yongchang Qiu, Matthew J Whitters, Kathleen N Tomkinson, Kyri Dunussi-Joannopoulos, Beatriz M Carreno, Mary Collins, Neil M Wolfman.
Abstract
IL-17F and IL-17A are members of the IL-17 pro-inflammatory cytokine family. IL-17A has been implicated in the pathogenesis of autoimmune diseases. IL-17F is a disulfide-linked dimer that contains a cysteine-knot motif. We hypothesized that IL-17F and IL-17A could form a heterodimer due to their sequence homology and overlapping pattern of expression. We evaluated the structure of recombinant IL-17F and IL-17A proteins, as well as that of natural IL-17F and IL-17A derived from activated human CD4+ T cells, by enzyme-linked immunosorbent assay, immunoprecipitation followed by Western blotting, and mass spectrometry. We find that both IL-17F and IL-17A can form both homodimeric and heterodimeric proteins when expressed in a recombinant system, and that all forms of the recombinant proteins have in vitro functional activity. Furthermore, we find that in addition to the homodimers of IL-17F and IL-17A, activated human CD4+ T cells also produce the IL-17F/IL-17A heterodimer. These data suggest that the IL-17F/IL-17A heterodimer may contribute to the T cell-mediated immune responses.Entities:
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Year: 2007 PMID: 17355969 DOI: 10.1074/jbc.M700499200
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157