TSLP links intestinal nutrient sensing with amplification of the ILC2-tuft cell circuit

Nat Immunol. 2025 Dec;26(12):2218-2226. doi: 10.1038/s41590-025-02328-y. Epub 2025 Nov 12.

Abstract

Group 2 innate lymphocytes (ILC2s) are prevalent in small intestine but their role during homeostasis is unclear. Here we show that thymic stromal lymphopoietin (TSLP)-a cytokine implicated in ILC2 activation-is expressed constitutively in subepithelial fibroblasts, including telocytes and crypt-associated trophocytes, which are specialized fibroblasts necessary to sustain epithelial identity. Feeding increases TSLP and induces ILC2 type 2 cytokines that are attenuated by deletion of TSLP in fibroblasts or TSLP receptor on ILC2s. Both mouse and human intestinal fibroblasts express receptors for glucagon-like peptide-2 (GLP-2)-an intestinotrophic growth factor released by enteroendocrine cells following food intake. GLP-2 promotes intestinal TSLP in mouse and human intestinal fibroblasts, and TSLP-dependent ILC2 activation and tuft cell hyperplasia in mice, thus linking nutrient detection with ILC2-mediated amplification of the tuft cell chemosensory circuit that promotes epithelial surveillance of ingested cargo.

MeSH terms

  • Animals
  • Cytokines* / genetics
  • Cytokines* / immunology
  • Cytokines* / metabolism
  • Fibroblasts* / immunology
  • Fibroblasts* / metabolism
  • Humans
  • Immunity, Innate
  • Intestinal Mucosa* / immunology
  • Intestinal Mucosa* / metabolism
  • Intestine, Small* / immunology
  • Lymphocytes* / immunology
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Nutrients / metabolism
  • Thymic Stromal Lymphopoietin
  • Tuft Cells

Substances

  • Cytokines
  • Thymic Stromal Lymphopoietin
  • Nutrients