A Novel Organoid Model of Damage and Repair Identifies HNF4α as a Critical Regulator of Intestinal Epithelial Regeneration

Cell Mol Gastroenterol Hepatol. 2020;10(2):209-223. doi: 10.1016/j.jcmgh.2020.02.007. Epub 2020 Mar 5.

Abstract

Background & aims: Recent evidence has suggested that the intact intestinal epithelial barrier protects our body from a range of immune-mediated diseases. The epithelial layer has an impressive ability to reconstitute and repair upon damage and this process of repair increasingly is seen as a therapeutic target. In vitro models to study this process in primary intestinal cells are lacking.

Methods: We established and characterized an in vitro model of intestinal damage and repair by applying γ-radiation on small-intestinal organoids. We then used this model to identify novel regulators of intestinal regeneration.

Results: We identified hepatocyte nuclear factor 4α (HNF4α) as a pivotal upstream regulator of the intestinal regenerative response. Organoids lacking Hnf4a were not able to propagate in vitro. Importantly, intestinal Hnf4a knock-out mice showed impaired regeneration after whole-body irradiation, confirming intestinal organoids as a valuable alternative to in vivo studies.

Conclusions: In conclusion, we established and validated an in vitro damage-repair model and identified HNF4α as a crucial regulator of intestinal regeneration. Transcript profiling: GSE141515 and GSE141518.

Keywords: Irradiation; Organoids; Regeneration.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cells, Cultured
  • Hepatocyte Nuclear Factor 4 / genetics
  • Hepatocyte Nuclear Factor 4 / metabolism*
  • Intestinal Mucosa / pathology*
  • Intestinal Mucosa / radiation effects
  • Intestine, Small / pathology*
  • Intestine, Small / radiation effects
  • Male
  • Mice
  • Mice, Knockout
  • Organoids
  • Primary Cell Culture
  • Radiation Injuries, Experimental
  • Regeneration*

Substances

  • Hepatocyte Nuclear Factor 4
  • Hnf4a protein, mouse