Secreted stromal protein ISLR promotes intestinal regeneration by suppressing epithelial Hippo signaling

EMBO J. 2020 Apr 1;39(7):e103255. doi: 10.15252/embj.2019103255. Epub 2020 Mar 4.

Abstract

The Hippo-YAP signaling pathway plays an essential role in epithelial cells during intestinal regeneration and tumorigenesis. However, the molecular mechanism linking stromal signals to YAP-mediated intestinal regeneration and tumorigenesis is poorly defined. Here, we report a stroma-epithelium ISLR-YAP signaling axis essential for stromal cells to modulate epithelial cell growth during intestinal regeneration and tumorigenesis. Specifically, upon inflammation and in cancer, an oncogenic transcription factor ETS1 in stromal cells induces expression of a secreted protein ISLR that can inhibit Hippo signaling and activate YAP in epithelial cells. Deletion of Islr in stromal cells in mice markedly impaired intestinal regeneration and suppressed tumorigenesis in the colon. Moreover, the expression of stromal cell-specific ISLR and ETS1 significantly increased in inflamed mucosa of human IBD patients and in human colorectal adenocarcinoma, accounting for the epithelial YAP hyperactivation. Collectively, our findings provide new insights into the signaling crosstalk between stroma and epithelium during tissue regeneration and tumorigenesis.

Keywords: Hippo signaling; ISLR; colorectal cancer; intestinal regeneration; stroma-epithelia crosstalk.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Colorectal Neoplasms / genetics
  • Colorectal Neoplasms / metabolism*
  • Disease Models, Animal
  • Gene Knockout Techniques
  • HCT116 Cells
  • HEK293 Cells
  • HT29 Cells
  • Hippo Signaling Pathway
  • Humans
  • Immunoglobulins / genetics*
  • Immunoglobulins / metabolism*
  • Inflammatory Bowel Diseases / genetics
  • Inflammatory Bowel Diseases / metabolism*
  • Intestinal Mucosa / metabolism
  • Male
  • Mice
  • Mutation
  • Promoter Regions, Genetic
  • Protein Serine-Threonine Kinases / metabolism
  • Proto-Oncogene Protein c-ets-1 / metabolism*
  • Signal Transduction

Substances

  • ETS1 protein, human
  • ISLR protein, human
  • Immunoglobulins
  • Proto-Oncogene Protein c-ets-1
  • Protein Serine-Threonine Kinases

Associated data

  • GEO/GSE135259
  • GEO/GSE135280