Nature Communications · 2023 · 48 citations · 38 references
Life SciencesImmunologyMolecular BiologyEpigeneticsInflammationTranscriptional RegulationCytokine BiologyImmune Gene RegulationImmune RegulationInflammatory Cell ResponsesInflammatory Response RegulationInflammatory SignalingAirway Inflammation CorrelatesAirway Inflammation ModulationAllergic Airway InflammationAsthma PathophysiologyInflammatory ChemokinesPro-inflammatory ChemokinesSirtuin RegulationTherapeutic Target Identification
Dysregulation of IL-17A is closely associated with airway inflammation and remodeling in severe asthma. However, the molecular mechanisms by which IL-17A is regulated remain unclear. Here we identify epithelial sirtuin 6 (SIRT6) as an epigenetic regulator that governs IL-17A pathogenicity in severe asthma. Mice with airway epithelial cell-specific deletion of Sirt6 are protected against allergen-induced airway inflammation and remodeling via inhibiting IL-17A-mediated inflammatory chemokines and mesenchymal reprogramming. Mechanistically, SIRT6 directly interacts with RORγt and mediates RORγt deacetylation at lysine 192 via its PPXY motifs. SIRT6 promotes RORγt recruitment to the IL-17A gene promoter and enhances its transcription. In severe asthma patients, high expression of SIRT6 positively correlates with airway remodeling and disease severity. SIRT6 inhibitor (OSS_128167) treatment significantly attenuates airway inflammation and remodeling in mice. Collectively, these results uncover a function for SIRT6 in regulating IL-17A pathogenicity in severe asthma, implicating SIRT6 as a potential therapeutic target for severe asthma.
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