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Notch signaling in the collecting duct regulates renal tubulointerstitial fibrosis induced by unilateral ureteral obstruction in mice
BACKGROUND/AIMS: Mind bomb-1 (Mib1) encodes an E3 ubiquitin ligase, which is required for the initiation of Notch signaling. Recently, it was demonstrated that the renal collecting duct plays an important role in renal fibrosis. Here, we investigated the role of Notch signaling in renal fibrosis usi...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Association of Internal Medicine
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6030409/ https://www.ncbi.nlm.nih.gov/pubmed/28602064 http://dx.doi.org/10.3904/kjim.2016.230 |
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author | Choi, Arum Nam, Sun Ah Kim, Wan-Young Park, Sang Hee Kim, Hyang Yang, Chul Woo Kim, Jin Kim, Yong Kyun |
author_facet | Choi, Arum Nam, Sun Ah Kim, Wan-Young Park, Sang Hee Kim, Hyang Yang, Chul Woo Kim, Jin Kim, Yong Kyun |
author_sort | Choi, Arum |
collection | PubMed |
description | BACKGROUND/AIMS: Mind bomb-1 (Mib1) encodes an E3 ubiquitin ligase, which is required for the initiation of Notch signaling. Recently, it was demonstrated that the renal collecting duct plays an important role in renal fibrosis. Here, we investigated the role of Notch signaling in renal fibrosis using conditional knockout mice with the specific ablation of Mib1 in renal collecting duct principal cells. METHODS: Mib1-floxed mice (Mib1(f/f)) were crossed with aquaporin 2 (AQP2)-Cre mice in order to generate principal cell-specific Mib1 knockout mice (Mib1(f/f) :AQP2-Cre(+)). Unilateral ureteral obstruction (UUO) was performed, and mice were sacrificed 7 days after UUO. RESULTS: After performing the UUO, renal tubulointerstitial fibrosis and the expression of transforming growth factor β were markedly enhanced in the obstructed kidneys of Mib1(f/f) mice compared with the sham-operated kidney of Mib1(f/f) mice. These changes were shown to be even more pronounced in the obstructed kidneys of Mib1(f/f) :AQP2-Cre(+) mice than in those of the Mib1(f/f) mice . Furthermore, the number of TUNNEL-positive cells in renal collecting duct was higher in the obstructed kidneys of Mib1(f/f) :AQP2-Cre(+) mice than in the kidneys of Mib1(f/f) mice. CONCLUSIONS: Notch signaling in the renal collecting duct plays an important role in the regulation of renal tubulointerstitial fibrosis and apoptosis after UUO. |
format | Online Article Text |
id | pubmed-6030409 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Korean Association of Internal Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-60304092018-07-06 Notch signaling in the collecting duct regulates renal tubulointerstitial fibrosis induced by unilateral ureteral obstruction in mice Choi, Arum Nam, Sun Ah Kim, Wan-Young Park, Sang Hee Kim, Hyang Yang, Chul Woo Kim, Jin Kim, Yong Kyun Korean J Intern Med Original Article BACKGROUND/AIMS: Mind bomb-1 (Mib1) encodes an E3 ubiquitin ligase, which is required for the initiation of Notch signaling. Recently, it was demonstrated that the renal collecting duct plays an important role in renal fibrosis. Here, we investigated the role of Notch signaling in renal fibrosis using conditional knockout mice with the specific ablation of Mib1 in renal collecting duct principal cells. METHODS: Mib1-floxed mice (Mib1(f/f)) were crossed with aquaporin 2 (AQP2)-Cre mice in order to generate principal cell-specific Mib1 knockout mice (Mib1(f/f) :AQP2-Cre(+)). Unilateral ureteral obstruction (UUO) was performed, and mice were sacrificed 7 days after UUO. RESULTS: After performing the UUO, renal tubulointerstitial fibrosis and the expression of transforming growth factor β were markedly enhanced in the obstructed kidneys of Mib1(f/f) mice compared with the sham-operated kidney of Mib1(f/f) mice. These changes were shown to be even more pronounced in the obstructed kidneys of Mib1(f/f) :AQP2-Cre(+) mice than in those of the Mib1(f/f) mice . Furthermore, the number of TUNNEL-positive cells in renal collecting duct was higher in the obstructed kidneys of Mib1(f/f) :AQP2-Cre(+) mice than in the kidneys of Mib1(f/f) mice. CONCLUSIONS: Notch signaling in the renal collecting duct plays an important role in the regulation of renal tubulointerstitial fibrosis and apoptosis after UUO. The Korean Association of Internal Medicine 2018-07 2017-05-26 /pmc/articles/PMC6030409/ /pubmed/28602064 http://dx.doi.org/10.3904/kjim.2016.230 Text en Copyright © 2018 The Korean Association of Internal Medicine This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Choi, Arum Nam, Sun Ah Kim, Wan-Young Park, Sang Hee Kim, Hyang Yang, Chul Woo Kim, Jin Kim, Yong Kyun Notch signaling in the collecting duct regulates renal tubulointerstitial fibrosis induced by unilateral ureteral obstruction in mice |
title | Notch signaling in the collecting duct regulates renal tubulointerstitial fibrosis induced by unilateral ureteral obstruction in mice |
title_full | Notch signaling in the collecting duct regulates renal tubulointerstitial fibrosis induced by unilateral ureteral obstruction in mice |
title_fullStr | Notch signaling in the collecting duct regulates renal tubulointerstitial fibrosis induced by unilateral ureteral obstruction in mice |
title_full_unstemmed | Notch signaling in the collecting duct regulates renal tubulointerstitial fibrosis induced by unilateral ureteral obstruction in mice |
title_short | Notch signaling in the collecting duct regulates renal tubulointerstitial fibrosis induced by unilateral ureteral obstruction in mice |
title_sort | notch signaling in the collecting duct regulates renal tubulointerstitial fibrosis induced by unilateral ureteral obstruction in mice |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6030409/ https://www.ncbi.nlm.nih.gov/pubmed/28602064 http://dx.doi.org/10.3904/kjim.2016.230 |
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