SMYD3-catalyzed dimethylation of gasdermin D at lysine 43 promotes pyroptosis and inflammatory responses

Gasdermin D (GSDMD), a key pyroptosis effector downstream of inflammasome activation, undergoes precise regulation by multiple posttranslational modifications. Here, we identify SMYD3, a lysine methyltransferase, as a positive regulator of GSDMD. SMYD3 interacts with GSDMD and catalyzes its dimethylation at lysine 43. This modification promotes GSDMD cleavage by caspases, leading to increased oligomerization and membrane localization of GSDMD N-terminal fragment (GSDMD-NT), which ultimately induces pyroptosis. Disrupting or inhibiting SMYD3 alleviates overactivated inflammation, thereby protecting against lipopolysaccharide-induced death in mice and zebrafish. Our findings reveal a role for SMYD3 in regulating the inflammatory response and shed light on a new mechanism that modulates GSDMD-mediated pyroptosis.

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Publication Details

Journal
Proceedings of the National Academy of Sciences
Published
2026-10-27
DOI
https://doi.org/10.1073/pnas.2616180123
Primary Topic
Inflammasome and immune disorders
Type
article
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article

SMYD3-catalyzed dimethylation of gasdermin D at lysine 43 promotes pyroptosis and inflammatory responses

Chunchun Zhu, Xiaoli Zeng, Shuke Jia, Wuhan Xiao et al.
1 links
Proceedings of the National Academy of Sciences
Inflammasome and immune disorders
article

SMYD3-catalyzed dimethylation of gasdermin D at lysine 43 promotes pyroptosis and inflammatory responses

Chunchun Zhu, Xiaoli Zeng, Shuke Jia, Wuhan Xiao, 于乐乐, Xueyi Sun, Xing Liu, Zixuan Wang, Hongyan Deng, Yiman Luo, Yuhan Xiang, Wen Liu
article en

Abstract

Gasdermin D (GSDMD), a key pyroptosis effector downstream of inflammasome activation, undergoes precise regulation by multiple posttranslational modifications. Here, we identify SMYD3, a lysine methyltransferase, as a positive regulator of GSDMD. SMYD3 interacts with GSDMD and catalyzes its dimethylation at lysine 43. This modification promotes GSDMD cleavage by caspases, leading to increased oligomerization and membrane localization of GSDMD N-terminal fragment (GSDMD-NT), which ultimately induces pyroptosis. Disrupting or inhibiting SMYD3 alleviates overactivated inflammation, thereby protecting against lipopolysaccharide-induced death in mice and zebrafish. Our findings reveal a role for SMYD3 in regulating the inflammatory response and shed light on a new mechanism that modulates GSDMD-mediated pyroptosis.

Proceedings of the National Academy of SciencesVol. 123(44)
Chinese Academy of Sciences (CN), Institute of Hydrobiology (CN), Qingdao National Laboratory for Marine Science and Technology (CN), University of Chinese Academy of Sciences (CN)
Good health and well-being
Openalex Percentile: Top 22%
Inflammasome and immune disorders
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