Cold-induced changes in gene expression in brown adipose tissue, white adipose tissue and liver

Cold exposure imposes a metabolic challenge to mammals that is met by a coordinated response in different tissues to prevent hypothermia. This study reports a transcriptomic analysis in brown adipose tissue (BAT), white adipose (WAT) and liver of mice in response to 24 h cold exposure at 8°C. Expres...

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Main Authors: Shore, Andrew M., Karamitri, Angeliki, Kemp, Paul, Speakman, John R., Graham, Neil S., Lomax, Michael A.
Format: Article
Published: Public Library of Science 2013
Online Access:https://eprints.nottingham.ac.uk/2532/
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author Shore, Andrew M.
Karamitri, Angeliki
Kemp, Paul
Speakman, John R.
Graham, Neil S.
Lomax, Michael A.
author_facet Shore, Andrew M.
Karamitri, Angeliki
Kemp, Paul
Speakman, John R.
Graham, Neil S.
Lomax, Michael A.
author_sort Shore, Andrew M.
building Nottingham Research Data Repository
collection Online Access
description Cold exposure imposes a metabolic challenge to mammals that is met by a coordinated response in different tissues to prevent hypothermia. This study reports a transcriptomic analysis in brown adipose tissue (BAT), white adipose (WAT) and liver of mice in response to 24 h cold exposure at 8°C. Expression of 1895 genes were significantly (P<0.05) up- or down-regulated more than two fold by cold exposure in all tissues but only 5 of these genes were shared by all three tissues, and only 19, 14 and 134 genes were common between WAT and BAT, WAT and liver, and BAT and liver, respectively. We confirmed using qRT-PCR, the increased expression of a number of characteristic BAT genes during cold exposure. In both BAT and the liver, the most common direction of change in gene expression was suppression (496 genes in BAT and 590 genes in liver). Gene ontology analysis revealed for the first time significant (P<0.05) down regulation in response to cold, of genes involved in oxidoreductase activity, lipid metabolic processes and protease inhibitor activity, in both BAT and liver, but not WAT. The results reveal an unexpected importance of down regulation of cytochrome P450 gene expression and apolipoprotein, in both BAT and liver, but not WAT, in response to cold exposure. Pathway analysis suggests a model in which down regulation of the nuclear transcription factors HNF4α and PPARα in both BAT and liver may orchestrate the down regulation of genes involved in lipoprotein and steroid metabolism as well as Phase I enzymes belonging to the cytochrome P450 group in response to cold stress in mice. We propose that the response to cold stress involves decreased gene expression in a range of cellular processes in order to maximise pathways involved in heat production.
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spelling nottingham-25322024-08-15T15:14:17Z https://eprints.nottingham.ac.uk/2532/ Cold-induced changes in gene expression in brown adipose tissue, white adipose tissue and liver Shore, Andrew M. Karamitri, Angeliki Kemp, Paul Speakman, John R. Graham, Neil S. Lomax, Michael A. Cold exposure imposes a metabolic challenge to mammals that is met by a coordinated response in different tissues to prevent hypothermia. This study reports a transcriptomic analysis in brown adipose tissue (BAT), white adipose (WAT) and liver of mice in response to 24 h cold exposure at 8°C. Expression of 1895 genes were significantly (P<0.05) up- or down-regulated more than two fold by cold exposure in all tissues but only 5 of these genes were shared by all three tissues, and only 19, 14 and 134 genes were common between WAT and BAT, WAT and liver, and BAT and liver, respectively. We confirmed using qRT-PCR, the increased expression of a number of characteristic BAT genes during cold exposure. In both BAT and the liver, the most common direction of change in gene expression was suppression (496 genes in BAT and 590 genes in liver). Gene ontology analysis revealed for the first time significant (P<0.05) down regulation in response to cold, of genes involved in oxidoreductase activity, lipid metabolic processes and protease inhibitor activity, in both BAT and liver, but not WAT. The results reveal an unexpected importance of down regulation of cytochrome P450 gene expression and apolipoprotein, in both BAT and liver, but not WAT, in response to cold exposure. Pathway analysis suggests a model in which down regulation of the nuclear transcription factors HNF4α and PPARα in both BAT and liver may orchestrate the down regulation of genes involved in lipoprotein and steroid metabolism as well as Phase I enzymes belonging to the cytochrome P450 group in response to cold stress in mice. We propose that the response to cold stress involves decreased gene expression in a range of cellular processes in order to maximise pathways involved in heat production. Public Library of Science 2013-07-22 Article PeerReviewed Shore, Andrew M., Karamitri, Angeliki, Kemp, Paul, Speakman, John R., Graham, Neil S. and Lomax, Michael A. (2013) Cold-induced changes in gene expression in brown adipose tissue, white adipose tissue and liver. PLoS ONE, 8 (7). e68933/1-e68933/9. ISSN 1932-6203 http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0068933 doi:10.1371/journal.pone.0068933 doi:10.1371/journal.pone.0068933
spellingShingle Shore, Andrew M.
Karamitri, Angeliki
Kemp, Paul
Speakman, John R.
Graham, Neil S.
Lomax, Michael A.
Cold-induced changes in gene expression in brown adipose tissue, white adipose tissue and liver
title Cold-induced changes in gene expression in brown adipose tissue, white adipose tissue and liver
title_full Cold-induced changes in gene expression in brown adipose tissue, white adipose tissue and liver
title_fullStr Cold-induced changes in gene expression in brown adipose tissue, white adipose tissue and liver
title_full_unstemmed Cold-induced changes in gene expression in brown adipose tissue, white adipose tissue and liver
title_short Cold-induced changes in gene expression in brown adipose tissue, white adipose tissue and liver
title_sort cold-induced changes in gene expression in brown adipose tissue, white adipose tissue and liver
url https://eprints.nottingham.ac.uk/2532/
https://eprints.nottingham.ac.uk/2532/
https://eprints.nottingham.ac.uk/2532/