| Literature DB >> 25616107 |
Maili Zimmermann1, Francisco Bianchetto Aguilera1, Monica Castellucci1, Marzia Rossato1, Sara Costa1, Claudio Lunardi2, Renato Ostuni3, Giampiero Girolomoni4, Gioacchino Natoli3, Flavia Bazzoni1, Nicola Tamassia1, Marco A Cassatella1.
Abstract
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.Entities:
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Year: 2015 PMID: 25616107 DOI: 10.1038/ncomms7061
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919