Intestinal epithelial Gasdermin C is induced by IL-4R/STAT6 signaling but is dispensable for gut immune homeostasis

Sci Rep. 2024 Nov 3;14(1):26522. doi: 10.1038/s41598-024-78336-z.

Abstract

Gasdermin C is one of the least studied members of the gasdermin family of proteins, known for their critical involvement in pyroptosis and host defense. Furthermore, evidence for the role of Gasdermin C in the intestine is scarce and partly controversial. Here, we tested the functional role of Gasdermin C in intestinal homeostasis, inflammation and tumorigenesis. : We studied Gasdermin C in response to cytokines in intestinal organoids. We evaluated epithelial differentiation, cell death and immune infiltration under steady state conditions in a new mouse line deficient in Gasdermin C. The role of Gasdermin C was analyzed in acute colitis, infection and colitis-associated cancer. Gasdemin C is highly expressed in the intestinal epithelium and strongly induced by the type 2 cytokines IL-4 and IL-13 in a STAT6-dependent manner. Gasdermin C-deficient mice show no changes in tissue architecture and epithelial homeostasis. Epithelial organoids deficient in Gasdermin C develop normally and show no alterations in proliferation or cell death. No changes were found in models of acute colitis, type 2 intestinal infection and colitis-associated cancer. Gasdermin C genes are upregulated by type 2 immunity, yet appear dispensable for the development of intestinal inflammation, infection and colitis-associated cancer.

Keywords: Gasdermin; Gut pathology; Intestinal homeostasis.

MeSH terms

  • Animals
  • Colitis* / genetics
  • Colitis* / immunology
  • Colitis* / metabolism
  • Colitis* / pathology
  • Gasdermins
  • Homeostasis*
  • Humans
  • Intestinal Mucosa* / immunology
  • Intestinal Mucosa* / metabolism
  • Intestinal Mucosa* / pathology
  • Intracellular Signaling Peptides and Proteins / genetics
  • Intracellular Signaling Peptides and Proteins / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Organoids / metabolism
  • Phosphate-Binding Proteins / genetics
  • Phosphate-Binding Proteins / metabolism
  • STAT6 Transcription Factor* / genetics
  • STAT6 Transcription Factor* / metabolism
  • Signal Transduction*

Substances

  • STAT6 Transcription Factor
  • Stat6 protein, mouse
  • Phosphate-Binding Proteins
  • Gsdma3 protein, mouse
  • Gsdmd protein, mouse
  • Intracellular Signaling Peptides and Proteins
  • Gasdermins