Jwa participates the maintenance of intestinal epithelial homeostasis via ERK/FBXW7-mediated NOTCH1/PPARγ/STAT5 axis and acts as a novel putative aging related gene

Int J Biol Sci. 2022 Aug 29;18(14):5503-5521. doi: 10.7150/ijbs.72751. eCollection 2022.

Abstract

The intestinal epithelium is a rapid self-renewal and regenerated tissue of which the structural integrity is beneficial for maintaining health. The integrity of intestinal epithelium depends on the balance of cell proliferation, differentiation, migration, and the function of intestinal stem cells, which declines due to genetic defect or aging. Jwa participates in multiple cellular processes; it also responds to oxidative stress and repairs DNA damage. However, whether Jwa plays a role in maintaining the homeostasis of intestinal renewal and regeneration is not clear. In the present study, we firstly described that the deletion of Jwa disturbed the homeostasis of intestinal epithelial renewal and regeneration. Jwa deficiency promoted NOTCH1 degradation in the ERK/FBXW7-mediated ubiquitin-proteasome pathway, thus disturbing the PPARγ/STAT5 axis. These mechanisms might partially contribute to the reduction of intestinal stem cell function and alteration of intestinal epithelial cell lineage distribution, finally suppressing the renewal and regeneration of intestinal epithelium. Moreover, our results also revealed that Jwa was a novel putative aging related gene.

Keywords: Aging; Intestinal epithelial homeostasis; Intestinal stem cell; JWA; Notch signal; Ubiquitination.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • F-Box-WD Repeat-Containing Protein 7 / metabolism
  • Heat-Shock Proteins / genetics
  • Homeostasis / genetics
  • Intestinal Mucosa / metabolism
  • Membrane Transport Proteins / metabolism
  • PPAR gamma* / genetics
  • PPAR gamma* / metabolism
  • Proteasome Endopeptidase Complex / metabolism
  • STAT5 Transcription Factor* / metabolism
  • Ubiquitins / metabolism

Substances

  • F-Box-WD Repeat-Containing Protein 7
  • Heat-Shock Proteins
  • Membrane Transport Proteins
  • PPAR gamma
  • STAT5 Transcription Factor
  • Ubiquitins
  • Proteasome Endopeptidase Complex