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The combination of high glucose and LPS induces autophagy in bovine kidney epithelial cells via the Notch3/mTOR signaling pathway
BACKGROUND: Aside respiratory diseases, beef cattle may also suffer from serious kidney diseases after transportation. Hyperglycemia and gram-negative bacterial infection may be the main reasons why bovine is prone to severe kidney disease during transportation stress, however, the precise mechanism...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9367163/ https://www.ncbi.nlm.nih.gov/pubmed/35953831 http://dx.doi.org/10.1186/s12917-022-03395-1 |
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author | Cui, Yaocheng Guo, Hongrui Zhang, Qin Fang, Jing Xie, Yue Chen, Shiyi Ma, Xiaoping Gou, Liping Cui, Hengmin Geng, Yi Ye, Gang Zhong, Zhijun Ren, Zhihua Wang, Ya Deng, Junliang Yu, Shuming Cao, Suizhong Wang, Zhisheng Zuo, Zhicai |
author_facet | Cui, Yaocheng Guo, Hongrui Zhang, Qin Fang, Jing Xie, Yue Chen, Shiyi Ma, Xiaoping Gou, Liping Cui, Hengmin Geng, Yi Ye, Gang Zhong, Zhijun Ren, Zhihua Wang, Ya Deng, Junliang Yu, Shuming Cao, Suizhong Wang, Zhisheng Zuo, Zhicai |
author_sort | Cui, Yaocheng |
collection | PubMed |
description | BACKGROUND: Aside respiratory diseases, beef cattle may also suffer from serious kidney diseases after transportation. Hyperglycemia and gram-negative bacterial infection may be the main reasons why bovine is prone to severe kidney disease during transportation stress, however, the precise mechanism is still unclear. The purpose of the current study is to explore whether the combined treatment of high glucose (HG) and lipopolysaccharide (LPS) could induce madin-darby bovine kidney (MDBK) cells injury and autophagy, as well as investigate the potential molecular mechanisms involved. RESULTS: As we discovered, the combined effect of HG and LPS decreased MDBK cells viability. And, HG and LPS combination also induced autophagy in MDBK cells, which was characterized by increasing the expression of LC3-II/I and Beclin1 and decreasing p62 expression. LC3 fluorescence signal formation was also significantly increased by HG and LPS combination treatment. Furthermore, we measured whether the mammalian target of rapamycin (mTOR) and the Notch3 signaling pathways were involved in HG and LPS-induced autophagy. The results showed that the combination of HG and LPS significantly increased the protein expression of Notch3 and decreased protein expression of p-mTOR, indicating that Notch3 and mTOR signaling pathways were activated. However, co-treatment with the Notch3 inhibitor (DAPT) could reverse the induction of autophagy, and increased the protein expression of p-mTOR. CONCLUSIONS: This study demonstrated that the combination effect of HG and LPS could induce autophagy in MDBK cells, and the Notch3/mTOR signaling pathway was involved in HG and LPS-induced autophagy. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12917-022-03395-1. |
format | Online Article Text |
id | pubmed-9367163 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-93671632022-08-12 The combination of high glucose and LPS induces autophagy in bovine kidney epithelial cells via the Notch3/mTOR signaling pathway Cui, Yaocheng Guo, Hongrui Zhang, Qin Fang, Jing Xie, Yue Chen, Shiyi Ma, Xiaoping Gou, Liping Cui, Hengmin Geng, Yi Ye, Gang Zhong, Zhijun Ren, Zhihua Wang, Ya Deng, Junliang Yu, Shuming Cao, Suizhong Wang, Zhisheng Zuo, Zhicai BMC Vet Res Research BACKGROUND: Aside respiratory diseases, beef cattle may also suffer from serious kidney diseases after transportation. Hyperglycemia and gram-negative bacterial infection may be the main reasons why bovine is prone to severe kidney disease during transportation stress, however, the precise mechanism is still unclear. The purpose of the current study is to explore whether the combined treatment of high glucose (HG) and lipopolysaccharide (LPS) could induce madin-darby bovine kidney (MDBK) cells injury and autophagy, as well as investigate the potential molecular mechanisms involved. RESULTS: As we discovered, the combined effect of HG and LPS decreased MDBK cells viability. And, HG and LPS combination also induced autophagy in MDBK cells, which was characterized by increasing the expression of LC3-II/I and Beclin1 and decreasing p62 expression. LC3 fluorescence signal formation was also significantly increased by HG and LPS combination treatment. Furthermore, we measured whether the mammalian target of rapamycin (mTOR) and the Notch3 signaling pathways were involved in HG and LPS-induced autophagy. The results showed that the combination of HG and LPS significantly increased the protein expression of Notch3 and decreased protein expression of p-mTOR, indicating that Notch3 and mTOR signaling pathways were activated. However, co-treatment with the Notch3 inhibitor (DAPT) could reverse the induction of autophagy, and increased the protein expression of p-mTOR. CONCLUSIONS: This study demonstrated that the combination effect of HG and LPS could induce autophagy in MDBK cells, and the Notch3/mTOR signaling pathway was involved in HG and LPS-induced autophagy. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12917-022-03395-1. BioMed Central 2022-08-11 /pmc/articles/PMC9367163/ /pubmed/35953831 http://dx.doi.org/10.1186/s12917-022-03395-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Cui, Yaocheng Guo, Hongrui Zhang, Qin Fang, Jing Xie, Yue Chen, Shiyi Ma, Xiaoping Gou, Liping Cui, Hengmin Geng, Yi Ye, Gang Zhong, Zhijun Ren, Zhihua Wang, Ya Deng, Junliang Yu, Shuming Cao, Suizhong Wang, Zhisheng Zuo, Zhicai The combination of high glucose and LPS induces autophagy in bovine kidney epithelial cells via the Notch3/mTOR signaling pathway |
title | The combination of high glucose and LPS induces autophagy in bovine kidney epithelial cells via the Notch3/mTOR signaling pathway |
title_full | The combination of high glucose and LPS induces autophagy in bovine kidney epithelial cells via the Notch3/mTOR signaling pathway |
title_fullStr | The combination of high glucose and LPS induces autophagy in bovine kidney epithelial cells via the Notch3/mTOR signaling pathway |
title_full_unstemmed | The combination of high glucose and LPS induces autophagy in bovine kidney epithelial cells via the Notch3/mTOR signaling pathway |
title_short | The combination of high glucose and LPS induces autophagy in bovine kidney epithelial cells via the Notch3/mTOR signaling pathway |
title_sort | combination of high glucose and lps induces autophagy in bovine kidney epithelial cells via the notch3/mtor signaling pathway |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9367163/ https://www.ncbi.nlm.nih.gov/pubmed/35953831 http://dx.doi.org/10.1186/s12917-022-03395-1 |
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