Peroxisome Elevation Induces Stem Cell Differentiation and Intestinal Epithelial Repair

Dev Cell. 2020 Apr 20;53(2):169-184.e11. doi: 10.1016/j.devcel.2020.03.002. Epub 2020 Apr 2.

Abstract

Epithelial-repair-dependent mucosal healing (MH) is associated with a more favorable prognosis for patients with inflammatory bowel disease (IBD). MH is accomplished via repair and regeneration of the intestinal epithelium. However, the mechanism underlying MH is ill defined. We found a striking upregulation of peroxisomes in the injured crypts of IBD patients. By increasing peroxisome levels in Drosophila midguts, we found that peroxisome elevation enhanced RAB7-dependent late endosome maturation, which then promoted stem and/or progenitor-cell differentiation via modulation of Janus Kinase (JAK) and Signal Transducer and Activator of Transcription (STAT)-SOX21A signaling. This in turn enhanced ISC-mediated regeneration. Importantly, RAB7 and SOX21 were upregulated in the crypts of IBD patients. Moreover, administration of drugs that increased peroxisome levels reversed the symptoms of dextran sulfate sodium (DSS)-induced colitis in mice. This study demonstrates a peroxisome-mediated epithelial repair mechanism, which opens a therapeutic avenue for the enhancement of MH in IBD patients.

Keywords: Drosophila; JAK and STAT signaling; SOX21A; differentiation; epithelial repair; inflammatory bowel disease; intestinal stem cells; late endosome maturation; peroxisome.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Animals
  • Cell Differentiation*
  • Colorectal Neoplasms / metabolism
  • Colorectal Neoplasms / pathology*
  • Drosophila melanogaster
  • Female
  • Gene Expression Regulation*
  • Humans
  • Inflammatory Bowel Diseases / metabolism
  • Inflammatory Bowel Diseases / pathology*
  • Intestinal Mucosa / cytology*
  • Intestinal Mucosa / injuries
  • Intestinal Mucosa / metabolism
  • Janus Kinases / genetics
  • Janus Kinases / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Middle Aged
  • Peroxisomes / physiology*
  • SOXB2 Transcription Factors / genetics
  • SOXB2 Transcription Factors / metabolism
  • STAT Transcription Factors / genetics
  • STAT Transcription Factors / metabolism
  • Stem Cells / cytology*
  • Young Adult
  • rab GTP-Binding Proteins / genetics
  • rab GTP-Binding Proteins / metabolism
  • rab7 GTP-Binding Proteins

Substances

  • SOXB2 Transcription Factors
  • STAT Transcription Factors
  • rab7 GTP-Binding Proteins
  • rab7 GTP-binding proteins, human
  • rab7 GTP-binding proteins, mouse
  • Janus Kinases
  • rab GTP-Binding Proteins