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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

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,...

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Autores principales: Li, Xiong, Liu, Jingwen, Zhou, Yan, Wang, Luman, Wen, Yifan, Ding, Kun, Zou, Lu, Liu, Xia, Li, Aiping, Wang, Yun, Fu, Heling, Huang, Min, Ding, Guoxian, Zhou, Jianwei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9461671/
https://www.ncbi.nlm.nih.gov/pubmed/36147468
http://dx.doi.org/10.7150/ijbs.72751
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author Li, Xiong
Liu, Jingwen
Zhou, Yan
Wang, Luman
Wen, Yifan
Ding, Kun
Zou, Lu
Liu, Xia
Li, Aiping
Wang, Yun
Fu, Heling
Huang, Min
Ding, Guoxian
Zhou, Jianwei
author_facet Li, Xiong
Liu, Jingwen
Zhou, Yan
Wang, Luman
Wen, Yifan
Ding, Kun
Zou, Lu
Liu, Xia
Li, Aiping
Wang, Yun
Fu, Heling
Huang, Min
Ding, Guoxian
Zhou, Jianwei
author_sort Li, Xiong
collection PubMed
description 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.
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spelling pubmed-94616712022-09-21 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 Li, Xiong Liu, Jingwen Zhou, Yan Wang, Luman Wen, Yifan Ding, Kun Zou, Lu Liu, Xia Li, Aiping Wang, Yun Fu, Heling Huang, Min Ding, Guoxian Zhou, Jianwei Int J Biol Sci Research Paper 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. Ivyspring International Publisher 2022-08-29 /pmc/articles/PMC9461671/ /pubmed/36147468 http://dx.doi.org/10.7150/ijbs.72751 Text en © The author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Li, Xiong
Liu, Jingwen
Zhou, Yan
Wang, Luman
Wen, Yifan
Ding, Kun
Zou, Lu
Liu, Xia
Li, Aiping
Wang, Yun
Fu, Heling
Huang, Min
Ding, Guoxian
Zhou, Jianwei
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
title 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
title_full 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
title_fullStr 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
title_full_unstemmed 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
title_short 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
title_sort 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
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9461671/
https://www.ncbi.nlm.nih.gov/pubmed/36147468
http://dx.doi.org/10.7150/ijbs.72751
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