| Literature DB >> 25419628 |
Elizabeth K Flynn1, Bojan Vilagos2, Udochuku Richson2, David E Symer1,3, Alan Aderem4, Christopher Schliehe2, Savitha Swaminanthan4, Berislav Bosnjak5, Lisa Bauer2, Richard K Kandasamy2, Isabel M Griesshammer2, Lindsay Kosack2, Frank Schmitz4, Vladimir Litvak6, James Sissons4, Alexander Lercher2, Anannya Bhattacharya2, Kseniya Khamina2, Anna L Trivett1, Lino Tessarollo1, Ildiko Mesteri7, Anastasiya Hladik2,8, Doron Merkler9,10, Stefan Kubicek2, Sylvia Knapp2,8, Michelle M Epstein5, Andreas Bergthaler2.
Abstract
Immune responses are tightly regulated to ensure efficient pathogen clearance while avoiding tissue damage. Here we report that Setdb2 was the only protein lysine methyltransferase induced during infection with influenza virus. Setdb2 expression depended on signaling via type I interferons, and Setdb2 repressed expression of the gene encoding the neutrophil attractant CXCL1 and other genes that are targets of the transcription factor NF-κB. This coincided with occupancy by Setdb2 at the Cxcl1 promoter, which in the absence of Setdb2 displayed diminished trimethylation of histone H3 Lys9 (H3K9me3). Mice with a hypomorphic gene-trap construct of Setdb2 exhibited increased infiltration of neutrophils during sterile lung inflammation and were less sensitive to bacterial superinfection after infection with influenza virus. This suggested that a Setdb2-mediated regulatory crosstalk between the type I interferons and NF-κB pathways represents an important mechanism for virus-induced susceptibility to bacterial superinfection.Entities:
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Year: 2014 PMID: 25419628 PMCID: PMC4320687 DOI: 10.1038/ni.3046
Source DB: PubMed Journal: Nat Immunol ISSN: 1529-2908 Impact factor: 25.606