Nature communications · 2015
Chromatin remodelling and autocrine TNFα are required for optimal interleukin-6 expression in activated human neutrophils.
СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод пока не подготовлен
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Zimmermann Maili, Aguilera Francisco Bianchetto, Castellucci Monica, Rossato Marzia, Costa Sara, Lunardi Claudio, Ostuni Renato, Girolomoni Giampiero, Natoli Gioacchino, Bazzoni Flavia, Tamassia Nicola, Cassatella Marco A
Аннотация
Controversy currently exists about the ability of human neutrophils to produce IL-6. Here, we show that the chromatin organization of the IL-6 genomic locus in human neutrophils is constitutively kept in an inactive configuration. However, we also show that upon exposure to stimuli that trigger chromatin remodelling at the IL-6 locus, such as ligands for TLR8 or, less efficiently, TLR4, highly purified neutrophils express and secrete IL-6. In TLR8-activated neutrophils, but not monocytes, IL-6 expression is preceded by the induction of a latent enhancer located 14 kb upstream of the IL-6 transcriptional start site. In addition, IL-6 induction is potentiated by endogenous TNFα, which prolongs the synthesis of the IκBζ co-activator and sustains C/EBPβ recruitment and histone acetylation at IL-6 regulatory regions. Altogether, these data clarify controversial literature on the ability of human neutrophils to generate IL-6 and uncover chromatin-dependent layers of regulation of IL-6 in these cells.
Предметные рубрики MeSH
Adaptor Proteins, Signal TransducingAnimalsAutocrine CommunicationChromatin Assembly and DisassemblyEnhancer Elements, GeneticGenetic LociGranulocyte Colony-Stimulating FactorHistonesHumansI-kappa B ProteinsImidazolesInflammationInterleukin 1 Receptor Antagonist ProteinInterleukin-12 Receptor beta 1 SubunitInterleukin-6LigandsMice, Inbred C57BLModels, BiologicalNeutrophil ActivationNeutrophilsNuclear ProteinsPeritoneumPromoter Regions, GeneticProtein BindingProtein Processing, Post-TranslationalRNA, MessengerToll-Like ReceptorsTranscription FactorsTumor Necrosis Factor-alpha