E3 ubiquitin ligase SYVN1 is a key positive regulator for GSDMD-mediated pyroptosis

Cell Death Dis. 2022 Feb 3;13(2):106. doi: 10.1038/s41419-022-04553-x.

Abstract

Gasdermin D (GSDMD) participates in the activation of inflammasomes and pyroptosis. Meanwhile, ubiquitination strictly regulates inflammatory responses. However, how ubiquitination regulates Gasdermin D activity is not well understood. In this study, we show that pyroptosis triggered by Gasdermin D is regulated through ubiquitination. Specifically, SYVN1, an E3 ubiquitin ligase of gasdermin D, promotes GSDMD-mediated pyroptosis. SYVN1 deficiency inhibits pyroptosis and subsequent LDH release and PI uptake. SYVN1 directly interacts with GSDMD, and mediates K27-linked polyubiquitination of GSDMD on K203 and K204 residues, promoting GSDMD-induced pyroptotic cell death. Thus, our findings revealed the essential role of SYVN1 in GSDMD-mediated pyroptosis. Overall, GSDMD ubiquitination is a potential therapeutic module for inflammatory diseases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Inflammasomes / metabolism
  • Intracellular Signaling Peptides and Proteins / genetics
  • Intracellular Signaling Peptides and Proteins / metabolism
  • Phosphate-Binding Proteins / metabolism
  • Pyroptosis* / physiology
  • Ubiquitin-Protein Ligases* / genetics
  • Ubiquitin-Protein Ligases* / metabolism

Substances

  • Inflammasomes
  • Intracellular Signaling Peptides and Proteins
  • Phosphate-Binding Proteins
  • Ubiquitin-Protein Ligases