Epithelial SIRT6 governs IL-17A pathogenicity and drives allergic airway inflammation and remodeling

Author:

Quan Jingyun,Wen Xiaoxia,Su Guomei,Zhong Yu,Huang Tong,Xiong Zhilin,Huang Jiewen,Lv Yingying,Li Shihai,Luo Shuhua,Luo Chaole,Cai Xin,Lai Xianwen,Xiang Yuanyuan,Zheng Song GuoORCID,Shao Yiming,Lin Haitao,Gao Xiao,Tang JingORCID,Lai Tianwen

Abstract

AbstractDysregulation 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.

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry,Multidisciplinary

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