Nature Communications (Dec 2023)

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

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

DOI
https://doi.org/10.1038/s41467-023-44179-x
Journal volume & issue
Vol. 14, no. 1
pp. 1 – 14

Abstract

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Abstract 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.