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Hepatic Gene Expression Profiling in Nrf2 Knockout Mice after Long-Term High-Fat Diet-Induced Obesity

Introduction. The transcription factor NFE2-related factor 2 (Nrf2) is a central regulator of antioxidant and detoxification gene expression in response to electrophilic or oxidative stress. Nrf2 has recently been shown to cross-talk with metabolic pathways, and its gene deletion protected mice from...

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Autores principales: Chartoumpekis, Dionysios V., Ziros, Panos G., Zaravinos, Apostolos, Iskrenova, Ralitsa P., Psyrogiannis, Agathoklis I., Kyriazopoulou, Venetsana E., Sykiotis, Gerasimos P., Habeos, Ioannis G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3654373/
https://www.ncbi.nlm.nih.gov/pubmed/23710285
http://dx.doi.org/10.1155/2013/340731
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author Chartoumpekis, Dionysios V.
Ziros, Panos G.
Zaravinos, Apostolos
Iskrenova, Ralitsa P.
Psyrogiannis, Agathoklis I.
Kyriazopoulou, Venetsana E.
Sykiotis, Gerasimos P.
Habeos, Ioannis G.
author_facet Chartoumpekis, Dionysios V.
Ziros, Panos G.
Zaravinos, Apostolos
Iskrenova, Ralitsa P.
Psyrogiannis, Agathoklis I.
Kyriazopoulou, Venetsana E.
Sykiotis, Gerasimos P.
Habeos, Ioannis G.
author_sort Chartoumpekis, Dionysios V.
collection PubMed
description Introduction. The transcription factor NFE2-related factor 2 (Nrf2) is a central regulator of antioxidant and detoxification gene expression in response to electrophilic or oxidative stress. Nrf2 has recently been shown to cross-talk with metabolic pathways, and its gene deletion protected mice from high-fat-diet-(HFD-) induced obesity and insulin resistance. This study aimed to identify potential Nrf2-regulated genes of metabolic interest by comparing gene expression profiles of livers of wild-type (WT) versus Nrf2 knockout (Nrf2-KO) mice after a long-term HFD. Methods. WT and Nrf2-KO mice were fed an HFD for 180 days; total RNA was prepared from liver and used for microarray analysis and quantitative real-time RT-PCR (qRT-PCR). Results. The microarray analysis identified 601 genes that were differentially expressed between WT and Nrf2-KO mice after long-term HFD. Selected genes, including ones known to be involved in metabolic regulation, were prioritized for verification by qRT-PCR: Cyp7a1 and Fabp5 were significantly overexpressed in Nrf2-KO mice; in contrast, Car, Cyp2b10, Lipocalin 13, Aquaporin 8, Cbr3, Me1, and Nqo1 were significantly underexpressed in Nrf2-KO mice. Conclusion. Transcriptome profiling after HFD-induced obesity confirms that Nrf2 is implicated in liver metabolic gene networks. The specific genes identified here may provide insights into Nrf2-dependent mechanisms of metabolic regulation.
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spelling pubmed-36543732013-05-24 Hepatic Gene Expression Profiling in Nrf2 Knockout Mice after Long-Term High-Fat Diet-Induced Obesity Chartoumpekis, Dionysios V. Ziros, Panos G. Zaravinos, Apostolos Iskrenova, Ralitsa P. Psyrogiannis, Agathoklis I. Kyriazopoulou, Venetsana E. Sykiotis, Gerasimos P. Habeos, Ioannis G. Oxid Med Cell Longev Research Article Introduction. The transcription factor NFE2-related factor 2 (Nrf2) is a central regulator of antioxidant and detoxification gene expression in response to electrophilic or oxidative stress. Nrf2 has recently been shown to cross-talk with metabolic pathways, and its gene deletion protected mice from high-fat-diet-(HFD-) induced obesity and insulin resistance. This study aimed to identify potential Nrf2-regulated genes of metabolic interest by comparing gene expression profiles of livers of wild-type (WT) versus Nrf2 knockout (Nrf2-KO) mice after a long-term HFD. Methods. WT and Nrf2-KO mice were fed an HFD for 180 days; total RNA was prepared from liver and used for microarray analysis and quantitative real-time RT-PCR (qRT-PCR). Results. The microarray analysis identified 601 genes that were differentially expressed between WT and Nrf2-KO mice after long-term HFD. Selected genes, including ones known to be involved in metabolic regulation, were prioritized for verification by qRT-PCR: Cyp7a1 and Fabp5 were significantly overexpressed in Nrf2-KO mice; in contrast, Car, Cyp2b10, Lipocalin 13, Aquaporin 8, Cbr3, Me1, and Nqo1 were significantly underexpressed in Nrf2-KO mice. Conclusion. Transcriptome profiling after HFD-induced obesity confirms that Nrf2 is implicated in liver metabolic gene networks. The specific genes identified here may provide insights into Nrf2-dependent mechanisms of metabolic regulation. Hindawi Publishing Corporation 2013 2013-04-18 /pmc/articles/PMC3654373/ /pubmed/23710285 http://dx.doi.org/10.1155/2013/340731 Text en Copyright © 2013 Dionysios V. Chartoumpekis et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Chartoumpekis, Dionysios V.
Ziros, Panos G.
Zaravinos, Apostolos
Iskrenova, Ralitsa P.
Psyrogiannis, Agathoklis I.
Kyriazopoulou, Venetsana E.
Sykiotis, Gerasimos P.
Habeos, Ioannis G.
Hepatic Gene Expression Profiling in Nrf2 Knockout Mice after Long-Term High-Fat Diet-Induced Obesity
title Hepatic Gene Expression Profiling in Nrf2 Knockout Mice after Long-Term High-Fat Diet-Induced Obesity
title_full Hepatic Gene Expression Profiling in Nrf2 Knockout Mice after Long-Term High-Fat Diet-Induced Obesity
title_fullStr Hepatic Gene Expression Profiling in Nrf2 Knockout Mice after Long-Term High-Fat Diet-Induced Obesity
title_full_unstemmed Hepatic Gene Expression Profiling in Nrf2 Knockout Mice after Long-Term High-Fat Diet-Induced Obesity
title_short Hepatic Gene Expression Profiling in Nrf2 Knockout Mice after Long-Term High-Fat Diet-Induced Obesity
title_sort hepatic gene expression profiling in nrf2 knockout mice after long-term high-fat diet-induced obesity
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3654373/
https://www.ncbi.nlm.nih.gov/pubmed/23710285
http://dx.doi.org/10.1155/2013/340731
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