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dc.contributor.author이수영*
dc.date.accessioned2016-08-27T04:08:22Z-
dc.date.available2016-08-27T04:08:22Z-
dc.date.issued2015*
dc.identifier.issn2041-1723*
dc.identifier.otherOAK-14793*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/217130-
dc.description.abstractTRAF6 is critical for the production of inflammatory cytokines in various TLR-mediated signalling pathways. However, it is poorly understood how TRAF6 regulates TLR3 responses. Here we demonstrate that GSK3 beta interacts with TRAF6 and positively regulates the TLR3-mediated signalling. Suppression of GSK3 beta expression or its kinase activity drastically reduces the production of inflammatory cytokines and the induction of c-Fos by decreasing ERK and p38 phosphorylation. GSK3 beta physically associates with TRAF6 in a TLR3 ligand poly I:C-dependent manner. TRAF6 is determined to be a direct E3 ligase for GSK3 beta, and TRAF6-mediated GSK3 beta ubiquitination is essential for poly I:C-dependent cytokine production by promoting the TLR3 adaptor protein TRIF-assembled signalling complex.*
dc.languageEnglish*
dc.publisherNATURE PUBLISHING GROUP*
dc.titleGlycogen synthase kinase 3 beta ubiquitination by TRAF6 regulates TLR3-mediated pro-inflammatory cytokine production*
dc.typeArticle*
dc.relation.volume6*
dc.relation.indexSCI*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.journaltitleNATURE COMMUNICATIONS*
dc.identifier.doi10.1038/ncomms7765*
dc.identifier.wosidWOS:000353702500005*
dc.identifier.scopusid2-s2.0-84926395603*
dc.author.googleKo, Ryeojin*
dc.author.googlePark, Jin Hee*
dc.author.googleHa, Hyunil*
dc.author.googleChoi, Yongwon*
dc.author.googleLee, Soo Young*
dc.contributor.scopusid이수영(53980218900;7409697278)*
dc.date.modifydate20240415140424*


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