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http://purl.uniprot.org/citations/31078730http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/31078730http://www.w3.org/2000/01/rdf-schema#comment"Oxidative stress and effector memory CD8+ T cells have been greatly implicated in vitiligo pathogenesis. However, the crosstalk between these two crucial pathogenic factors has been merely investigated. IL-15 has been regarded as an important cytokine exerting its facilitative effect on memory CD8+ T cells function in various autoimmune diseases. In the present study, we initially discovered that the IL-15 expression was significantly increased in vitiligo epidermis and highly associated with epidermal H2O2 content. In addition, epidermal IL-15 expression was mainly derived from keratinocytes. Then, we showed that oxidative stress promoted IL-15 and IL-15Rα expression as well as IL-15 trans-presentation by activating NF-κB signaling in keratinocytes. What's more, the trans-presented IL-15, rather than the secreted one, was accounted for the potentiation of CD8+ TEMs activation. We further investigated the mechanism underlying trans-presented IL-15 in potentiating CD8+ TEMs activation and found that the blockage of IL-15-JAK-STAT signaling could be a potent therapeutic approach. Taken together, our results demonstrate that oxidative stress-induced IL-15 trans-presentation in keratinocytes contributes to the activation of CD8+ TEMs, providing a novel mechanism by which oxidative stress initiates autoimmunity in vitiligo."xsd:string
http://purl.uniprot.org/citations/31078730http://purl.org/dc/terms/identifier"doi:10.1016/j.freeradbiomed.2019.05.011"xsd:string
http://purl.uniprot.org/citations/31078730http://purl.uniprot.org/core/author"Chen J."xsd:string
http://purl.uniprot.org/citations/31078730http://purl.uniprot.org/core/author"Chen X."xsd:string
http://purl.uniprot.org/citations/31078730http://purl.uniprot.org/core/author"Li C."xsd:string
http://purl.uniprot.org/citations/31078730http://purl.uniprot.org/core/author"Li K."xsd:string
http://purl.uniprot.org/citations/31078730http://purl.uniprot.org/core/author"Li S."xsd:string
http://purl.uniprot.org/citations/31078730http://purl.uniprot.org/core/author"Guo W."xsd:string
http://purl.uniprot.org/citations/31078730http://purl.uniprot.org/core/author"Guo S."xsd:string
http://purl.uniprot.org/citations/31078730http://purl.uniprot.org/core/author"Liu L."xsd:string
http://purl.uniprot.org/citations/31078730http://purl.uniprot.org/core/author"Gao T."xsd:string
http://purl.uniprot.org/citations/31078730http://purl.uniprot.org/core/author"Xiao Q."xsd:string
http://purl.uniprot.org/citations/31078730http://purl.uniprot.org/core/author"Cui T."xsd:string
http://purl.uniprot.org/citations/31078730http://purl.uniprot.org/core/author"Chang Y."xsd:string
http://purl.uniprot.org/citations/31078730http://purl.uniprot.org/core/author"Yi X."xsd:string
http://purl.uniprot.org/citations/31078730http://purl.uniprot.org/core/author"Jian Z."xsd:string
http://purl.uniprot.org/citations/31078730http://purl.uniprot.org/core/author"Kang P."xsd:string
http://purl.uniprot.org/citations/31078730http://purl.uniprot.org/core/date"2019"xsd:gYear
http://purl.uniprot.org/citations/31078730http://purl.uniprot.org/core/name"Free Radic Biol Med"xsd:string
http://purl.uniprot.org/citations/31078730http://purl.uniprot.org/core/pages"80-91"xsd:string
http://purl.uniprot.org/citations/31078730http://purl.uniprot.org/core/title"Oxidative stress-induced IL-15 trans-presentation in keratinocytes contributes to CD8+ T cells activation via JAK-STAT pathway in vitiligo."xsd:string
http://purl.uniprot.org/citations/31078730http://purl.uniprot.org/core/volume"139"xsd:string
http://purl.uniprot.org/citations/31078730http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/31078730
http://purl.uniprot.org/citations/31078730http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/31078730