RDF/XMLNTriplesTurtleShow queryShare
SubjectPredicateObject
http://purl.uniprot.org/citations/29244194http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/29244194http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/29244194http://www.w3.org/2000/01/rdf-schema#comment"AT-rich interactive domain-containing protein 5a (Arid5a) is an RNA-binding protein (RBP) required for autoimmunity via stabilization of interleukin-6 (Il6) and signal transducer and activator of transcription 3 (STAT3) mRNAs. However, the roles of Arid5a in Th17 cells and its association with autoimmunity remain unknown. Here, we show that the levels of Arid5a and OX40 are correlated in CD4+ T cells under Th17 conditions in an IL-6-dependent manner. Lack of Arid5a in T cells reduced OX40 expression levels and repressed IL-17 production in response to OX40 ligation. Arid5a stabilized OX40 mRNA by recognizing the alternative decay element (ADE)-like stem-loop (SL) in the 3' untranslated region (3'UTR). Interestingly, Arid5a impaired the RNA-destabilizing functions of Regnase-1 and Roquin-1 on OX40 ADE-like SL. In EAE, Arid5a-deficient mice exhibited resistance to EAE, with reduced OX40 expression in CD4+ T cells, and the number of CD4+ CD45+ T cells was decreased in CNS. Furthermore, ameliorated EAE was induced by adoptive transfer of Arid5a-/- encephalitogenic CD4+ T cells expressing less OX40 mRNA and producing less IL-17. In conclusion, our findings indicate that the Arid5a/OX40 axis in CD4+ T cells may have important implications in pathogenesis of autoimmune diseases such as EAE."xsd:string
http://purl.uniprot.org/citations/29244194http://purl.org/dc/terms/identifier"doi:10.1002/eji.201747109"xsd:string
http://purl.uniprot.org/citations/29244194http://purl.org/dc/terms/identifier"doi:10.1002/eji.201747109"xsd:string
http://purl.uniprot.org/citations/29244194http://purl.uniprot.org/core/author"Li S."xsd:string
http://purl.uniprot.org/citations/29244194http://purl.uniprot.org/core/author"Li S."xsd:string
http://purl.uniprot.org/citations/29244194http://purl.uniprot.org/core/author"Kishimoto T."xsd:string
http://purl.uniprot.org/citations/29244194http://purl.uniprot.org/core/author"Kishimoto T."xsd:string
http://purl.uniprot.org/citations/29244194http://purl.uniprot.org/core/author"Higa M."xsd:string
http://purl.uniprot.org/citations/29244194http://purl.uniprot.org/core/author"Higa M."xsd:string
http://purl.uniprot.org/citations/29244194http://purl.uniprot.org/core/author"Masuda K."xsd:string
http://purl.uniprot.org/citations/29244194http://purl.uniprot.org/core/author"Masuda K."xsd:string
http://purl.uniprot.org/citations/29244194http://purl.uniprot.org/core/author"Standley D.M."xsd:string
http://purl.uniprot.org/citations/29244194http://purl.uniprot.org/core/author"Standley D.M."xsd:string
http://purl.uniprot.org/citations/29244194http://purl.uniprot.org/core/author"Mohamed M."xsd:string
http://purl.uniprot.org/citations/29244194http://purl.uniprot.org/core/author"Mohamed M."xsd:string
http://purl.uniprot.org/citations/29244194http://purl.uniprot.org/core/author"Chalise J.P."xsd:string
http://purl.uniprot.org/citations/29244194http://purl.uniprot.org/core/author"Chalise J.P."xsd:string
http://purl.uniprot.org/citations/29244194http://purl.uniprot.org/core/author"Hanieh H."xsd:string
http://purl.uniprot.org/citations/29244194http://purl.uniprot.org/core/author"Hanieh H."xsd:string
http://purl.uniprot.org/citations/29244194http://purl.uniprot.org/core/author"Metwally H."xsd:string
http://purl.uniprot.org/citations/29244194http://purl.uniprot.org/core/author"Metwally H."xsd:string
http://purl.uniprot.org/citations/29244194http://purl.uniprot.org/core/author"Nyati K.K."xsd:string
http://purl.uniprot.org/citations/29244194http://purl.uniprot.org/core/author"Nyati K.K."xsd:string