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Metabolomic Changes of Human Proximal Tubular Cell Line in High Glucose Environment
Hyperglycemia causes mitochondrial damage renal tubular cells, which contribute to the progression of diabetic kidney disease. However, the metabolic aberration of renal tubular cells in an hyperglycemic milieu has not been fully elucidated. In this study, human proximal renal tubular cell line (HK-...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6851361/ https://www.ncbi.nlm.nih.gov/pubmed/31719648 http://dx.doi.org/10.1038/s41598-019-53214-1 |
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author | Wei, Pascal Zhongping Fung, Winston Wing-Shing Ng, Jack Kit-Chung Lai, Ka-Bik Luk, Cathy Choi-Wan Chow, Kai Ming Li, Philip Kam-Tao Szeto, Cheuk Chun |
author_facet | Wei, Pascal Zhongping Fung, Winston Wing-Shing Ng, Jack Kit-Chung Lai, Ka-Bik Luk, Cathy Choi-Wan Chow, Kai Ming Li, Philip Kam-Tao Szeto, Cheuk Chun |
author_sort | Wei, Pascal Zhongping |
collection | PubMed |
description | Hyperglycemia causes mitochondrial damage renal tubular cells, which contribute to the progression of diabetic kidney disease. However, the metabolic aberration of renal tubular cells in an hyperglycemic milieu has not been fully elucidated. In this study, human proximal renal tubular cell line (HK-2 cell) are incubated in glucose and mannitol at 5 mM or 25 mM. Cellular metabolome was determined by capillary electrophoresis time of flight mass spectrometer (CE-TOF/MS) and capillary electrophoresis-triple quadrupole mass spectrometry (CE-QqQMS). A total of 116 metabolites were quantified. Principal component analysis (PCA) revealed excellent clustering of metabolomic changes for different treatment conditions, and exposure to glucose at 5 and 25 mM lead to distinct metabolomic profiles as compared to samples treated with serum-free medium or mannitol as osmotic control. Hierarchical clustering analysis showed a number of characteristic changes in metabolic profile following exposure to 5 mM or 25 mM glucose. Notably, lactate-to-pyruvate ratio was significantly increased, while cellular levels of citric acid, α-ketoglutaric acid (i.e. 2-oxoglutaric acid), and fumaric acid were significantly reduced after exposure to glucose at 25 mM but not 5 mM. Moreover, cellular levels of reduced glutathione and total glutathione were significantly decreased, and S-adenosylmethionine (SAM) to S-adenosylhomocysteine (SAH) ratio was significantly increased after exposure to glucose 25 mM but not 5 mM. We conclude that in response to high glucose, HK-2 cells characteristic metabolomic changes, including increase in lactate-to-pyruvate ratio, reduction in Krebs cycle metabolites, reduction in glutathione antioxidant activity, and increase in cellular methylation potential. Our results may shed light on the pathogenesis of diabetic kidney disease, but the expression of glucose metabolism-related protein and enzyme activity in HK-2 cells after hyperglycemia condition need to be confirmed by further studies. |
format | Online Article Text |
id | pubmed-6851361 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-68513612019-11-19 Metabolomic Changes of Human Proximal Tubular Cell Line in High Glucose Environment Wei, Pascal Zhongping Fung, Winston Wing-Shing Ng, Jack Kit-Chung Lai, Ka-Bik Luk, Cathy Choi-Wan Chow, Kai Ming Li, Philip Kam-Tao Szeto, Cheuk Chun Sci Rep Article Hyperglycemia causes mitochondrial damage renal tubular cells, which contribute to the progression of diabetic kidney disease. However, the metabolic aberration of renal tubular cells in an hyperglycemic milieu has not been fully elucidated. In this study, human proximal renal tubular cell line (HK-2 cell) are incubated in glucose and mannitol at 5 mM or 25 mM. Cellular metabolome was determined by capillary electrophoresis time of flight mass spectrometer (CE-TOF/MS) and capillary electrophoresis-triple quadrupole mass spectrometry (CE-QqQMS). A total of 116 metabolites were quantified. Principal component analysis (PCA) revealed excellent clustering of metabolomic changes for different treatment conditions, and exposure to glucose at 5 and 25 mM lead to distinct metabolomic profiles as compared to samples treated with serum-free medium or mannitol as osmotic control. Hierarchical clustering analysis showed a number of characteristic changes in metabolic profile following exposure to 5 mM or 25 mM glucose. Notably, lactate-to-pyruvate ratio was significantly increased, while cellular levels of citric acid, α-ketoglutaric acid (i.e. 2-oxoglutaric acid), and fumaric acid were significantly reduced after exposure to glucose at 25 mM but not 5 mM. Moreover, cellular levels of reduced glutathione and total glutathione were significantly decreased, and S-adenosylmethionine (SAM) to S-adenosylhomocysteine (SAH) ratio was significantly increased after exposure to glucose 25 mM but not 5 mM. We conclude that in response to high glucose, HK-2 cells characteristic metabolomic changes, including increase in lactate-to-pyruvate ratio, reduction in Krebs cycle metabolites, reduction in glutathione antioxidant activity, and increase in cellular methylation potential. Our results may shed light on the pathogenesis of diabetic kidney disease, but the expression of glucose metabolism-related protein and enzyme activity in HK-2 cells after hyperglycemia condition need to be confirmed by further studies. Nature Publishing Group UK 2019-11-12 /pmc/articles/PMC6851361/ /pubmed/31719648 http://dx.doi.org/10.1038/s41598-019-53214-1 Text en © The Author(s) 2019 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Wei, Pascal Zhongping Fung, Winston Wing-Shing Ng, Jack Kit-Chung Lai, Ka-Bik Luk, Cathy Choi-Wan Chow, Kai Ming Li, Philip Kam-Tao Szeto, Cheuk Chun Metabolomic Changes of Human Proximal Tubular Cell Line in High Glucose Environment |
title | Metabolomic Changes of Human Proximal Tubular Cell Line in High Glucose Environment |
title_full | Metabolomic Changes of Human Proximal Tubular Cell Line in High Glucose Environment |
title_fullStr | Metabolomic Changes of Human Proximal Tubular Cell Line in High Glucose Environment |
title_full_unstemmed | Metabolomic Changes of Human Proximal Tubular Cell Line in High Glucose Environment |
title_short | Metabolomic Changes of Human Proximal Tubular Cell Line in High Glucose Environment |
title_sort | metabolomic changes of human proximal tubular cell line in high glucose environment |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6851361/ https://www.ncbi.nlm.nih.gov/pubmed/31719648 http://dx.doi.org/10.1038/s41598-019-53214-1 |
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