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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,...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2022
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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. |
format | Online Article Text |
id | pubmed-9461671 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
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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