Cargando…
A Quantitative HILIC–MS/MS Assay of the Metabolic Response of Huh-7 Cells Exposed to 2,3,7,8-Tetrachlorodibenzo-p-Dioxin
A hydrophilic interaction liquid chromatography (HILIC)–ultra high-pressure liquid chromatography (UHPLC) coupled with tandem mass spectrometry (MS/MS) method was developed and applied to profile metabolite changes in human Huh-7 cells exposed to the potent aryl hydrocarbon receptor (AHR) ligand 2,3...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6631636/ https://www.ncbi.nlm.nih.gov/pubmed/31226775 http://dx.doi.org/10.3390/metabo9060118 |
_version_ | 1783435564123422720 |
---|---|
author | Liu, Qing Cai, Jingwei Nichols, Robert G. Tian, Yuan Zhang, Jintao Smith, Philip B. Wang, Yan Yan, Chao Patterson, Andrew D. |
author_facet | Liu, Qing Cai, Jingwei Nichols, Robert G. Tian, Yuan Zhang, Jintao Smith, Philip B. Wang, Yan Yan, Chao Patterson, Andrew D. |
author_sort | Liu, Qing |
collection | PubMed |
description | A hydrophilic interaction liquid chromatography (HILIC)–ultra high-pressure liquid chromatography (UHPLC) coupled with tandem mass spectrometry (MS/MS) method was developed and applied to profile metabolite changes in human Huh-7 cells exposed to the potent aryl hydrocarbon receptor (AHR) ligand 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD). Comparisons of sensitivity (limit of detection as low as 0.01 µM) and reproducibility (84% of compounds had an interday relative standard deviation (RSD) less than 10.0%; 83% of compounds had an intraday RSD less than 15.0%) were assessed for all the metabolites. The exposure of Huh-7 cells to the hepatotoxic carcinogen TCDD at low doses (1 nM and 10 nM for 4 h and 24 h, respectively) was reflected by the disturbance of amino acid metabolism, energy metabolism (glycolysis, TCA cycle), and nucleic acid metabolism. TCDD caused a significant decrease in amino acids such as serine, alanine, and proline while promoting an increase in arginine levels with 24 h treatment. Energy metabolism intermediates such as phosphoenolpyruvate and acetyl–CoA and nucleosides such as UMP, XMP, and CMP were also markedly decreased. These results support the application of HILIC–UHPLC–MS/MS for robust and reliable analysis of the cellular response to environmentally relevant toxicants at lower doses. |
format | Online Article Text |
id | pubmed-6631636 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-66316362019-08-19 A Quantitative HILIC–MS/MS Assay of the Metabolic Response of Huh-7 Cells Exposed to 2,3,7,8-Tetrachlorodibenzo-p-Dioxin Liu, Qing Cai, Jingwei Nichols, Robert G. Tian, Yuan Zhang, Jintao Smith, Philip B. Wang, Yan Yan, Chao Patterson, Andrew D. Metabolites Article A hydrophilic interaction liquid chromatography (HILIC)–ultra high-pressure liquid chromatography (UHPLC) coupled with tandem mass spectrometry (MS/MS) method was developed and applied to profile metabolite changes in human Huh-7 cells exposed to the potent aryl hydrocarbon receptor (AHR) ligand 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD). Comparisons of sensitivity (limit of detection as low as 0.01 µM) and reproducibility (84% of compounds had an interday relative standard deviation (RSD) less than 10.0%; 83% of compounds had an intraday RSD less than 15.0%) were assessed for all the metabolites. The exposure of Huh-7 cells to the hepatotoxic carcinogen TCDD at low doses (1 nM and 10 nM for 4 h and 24 h, respectively) was reflected by the disturbance of amino acid metabolism, energy metabolism (glycolysis, TCA cycle), and nucleic acid metabolism. TCDD caused a significant decrease in amino acids such as serine, alanine, and proline while promoting an increase in arginine levels with 24 h treatment. Energy metabolism intermediates such as phosphoenolpyruvate and acetyl–CoA and nucleosides such as UMP, XMP, and CMP were also markedly decreased. These results support the application of HILIC–UHPLC–MS/MS for robust and reliable analysis of the cellular response to environmentally relevant toxicants at lower doses. MDPI 2019-06-20 /pmc/articles/PMC6631636/ /pubmed/31226775 http://dx.doi.org/10.3390/metabo9060118 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Liu, Qing Cai, Jingwei Nichols, Robert G. Tian, Yuan Zhang, Jintao Smith, Philip B. Wang, Yan Yan, Chao Patterson, Andrew D. A Quantitative HILIC–MS/MS Assay of the Metabolic Response of Huh-7 Cells Exposed to 2,3,7,8-Tetrachlorodibenzo-p-Dioxin |
title | A Quantitative HILIC–MS/MS Assay of the Metabolic Response of Huh-7 Cells Exposed to 2,3,7,8-Tetrachlorodibenzo-p-Dioxin |
title_full | A Quantitative HILIC–MS/MS Assay of the Metabolic Response of Huh-7 Cells Exposed to 2,3,7,8-Tetrachlorodibenzo-p-Dioxin |
title_fullStr | A Quantitative HILIC–MS/MS Assay of the Metabolic Response of Huh-7 Cells Exposed to 2,3,7,8-Tetrachlorodibenzo-p-Dioxin |
title_full_unstemmed | A Quantitative HILIC–MS/MS Assay of the Metabolic Response of Huh-7 Cells Exposed to 2,3,7,8-Tetrachlorodibenzo-p-Dioxin |
title_short | A Quantitative HILIC–MS/MS Assay of the Metabolic Response of Huh-7 Cells Exposed to 2,3,7,8-Tetrachlorodibenzo-p-Dioxin |
title_sort | quantitative hilic–ms/ms assay of the metabolic response of huh-7 cells exposed to 2,3,7,8-tetrachlorodibenzo-p-dioxin |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6631636/ https://www.ncbi.nlm.nih.gov/pubmed/31226775 http://dx.doi.org/10.3390/metabo9060118 |
work_keys_str_mv | AT liuqing aquantitativehilicmsmsassayofthemetabolicresponseofhuh7cellsexposedto2378tetrachlorodibenzopdioxin AT caijingwei aquantitativehilicmsmsassayofthemetabolicresponseofhuh7cellsexposedto2378tetrachlorodibenzopdioxin AT nicholsrobertg aquantitativehilicmsmsassayofthemetabolicresponseofhuh7cellsexposedto2378tetrachlorodibenzopdioxin AT tianyuan aquantitativehilicmsmsassayofthemetabolicresponseofhuh7cellsexposedto2378tetrachlorodibenzopdioxin AT zhangjintao aquantitativehilicmsmsassayofthemetabolicresponseofhuh7cellsexposedto2378tetrachlorodibenzopdioxin AT smithphilipb aquantitativehilicmsmsassayofthemetabolicresponseofhuh7cellsexposedto2378tetrachlorodibenzopdioxin AT wangyan aquantitativehilicmsmsassayofthemetabolicresponseofhuh7cellsexposedto2378tetrachlorodibenzopdioxin AT yanchao aquantitativehilicmsmsassayofthemetabolicresponseofhuh7cellsexposedto2378tetrachlorodibenzopdioxin AT pattersonandrewd aquantitativehilicmsmsassayofthemetabolicresponseofhuh7cellsexposedto2378tetrachlorodibenzopdioxin AT liuqing quantitativehilicmsmsassayofthemetabolicresponseofhuh7cellsexposedto2378tetrachlorodibenzopdioxin AT caijingwei quantitativehilicmsmsassayofthemetabolicresponseofhuh7cellsexposedto2378tetrachlorodibenzopdioxin AT nicholsrobertg quantitativehilicmsmsassayofthemetabolicresponseofhuh7cellsexposedto2378tetrachlorodibenzopdioxin AT tianyuan quantitativehilicmsmsassayofthemetabolicresponseofhuh7cellsexposedto2378tetrachlorodibenzopdioxin AT zhangjintao quantitativehilicmsmsassayofthemetabolicresponseofhuh7cellsexposedto2378tetrachlorodibenzopdioxin AT smithphilipb quantitativehilicmsmsassayofthemetabolicresponseofhuh7cellsexposedto2378tetrachlorodibenzopdioxin AT wangyan quantitativehilicmsmsassayofthemetabolicresponseofhuh7cellsexposedto2378tetrachlorodibenzopdioxin AT yanchao quantitativehilicmsmsassayofthemetabolicresponseofhuh7cellsexposedto2378tetrachlorodibenzopdioxin AT pattersonandrewd quantitativehilicmsmsassayofthemetabolicresponseofhuh7cellsexposedto2378tetrachlorodibenzopdioxin |