Cargando…

Global gene expression profiling of brown to white adipose tissue transformation in sheep reveals novel transcriptional components linked to adipose remodeling

BACKGROUND: Large mammals are capable of thermoregulation shortly after birth due to the presence of brown adipose tissue (BAT). The majority of BAT disappears after birth and is replaced by white adipose tissue (WAT). RESULTS: We analyzed the postnatal transformation of adipose in sheep with a time...

Descripción completa

Detalles Bibliográficos
Autores principales: Basse, Astrid L, Dixen, Karen, Yadav, Rachita, Tygesen, Malin P, Qvortrup, Klaus, Kristiansen, Karsten, Quistorff, Bjørn, Gupta, Ramneek, Wang, Jun, Hansen, Jacob B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4407871/
https://www.ncbi.nlm.nih.gov/pubmed/25887780
http://dx.doi.org/10.1186/s12864-015-1405-8
_version_ 1782367973465391104
author Basse, Astrid L
Dixen, Karen
Yadav, Rachita
Tygesen, Malin P
Qvortrup, Klaus
Kristiansen, Karsten
Quistorff, Bjørn
Gupta, Ramneek
Wang, Jun
Hansen, Jacob B
author_facet Basse, Astrid L
Dixen, Karen
Yadav, Rachita
Tygesen, Malin P
Qvortrup, Klaus
Kristiansen, Karsten
Quistorff, Bjørn
Gupta, Ramneek
Wang, Jun
Hansen, Jacob B
author_sort Basse, Astrid L
collection PubMed
description BACKGROUND: Large mammals are capable of thermoregulation shortly after birth due to the presence of brown adipose tissue (BAT). The majority of BAT disappears after birth and is replaced by white adipose tissue (WAT). RESULTS: We analyzed the postnatal transformation of adipose in sheep with a time course study of the perirenal adipose depot. We observed changes in tissue morphology, gene expression and metabolism within the first two weeks of postnatal life consistent with the expected transition from BAT to WAT. The transformation was characterized by massively decreased mitochondrial abundance and down-regulation of gene expression related to mitochondrial function and oxidative phosphorylation. Global gene expression profiling demonstrated that the time points grouped into three phases: a brown adipose phase, a transition phase and a white adipose phase. Between the brown adipose and the transition phase 170 genes were differentially expressed, and 717 genes were differentially expressed between the transition and the white adipose phase. Thirty-eight genes were shared among the two sets of differentially expressed genes. We identified a number of regulated transcription factors, including NR1H3, MYC, KLF4, ESR1, RELA and BCL6, which were linked to the overall changes in gene expression during the adipose tissue remodeling. Finally, the perirenal adipose tissue expressed both brown and brite/beige adipocyte marker genes at birth, the expression of which changed substantially over time. CONCLUSIONS: Using global gene expression profiling of the postnatal BAT to WAT transformation in sheep, we provide novel insight into adipose tissue plasticity in a large mammal, including identification of novel transcriptional components linked to adipose tissue remodeling. Moreover, our data set provides a useful resource for further studies in adipose tissue plasticity. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-1405-8) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-4407871
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-44078712015-04-24 Global gene expression profiling of brown to white adipose tissue transformation in sheep reveals novel transcriptional components linked to adipose remodeling Basse, Astrid L Dixen, Karen Yadav, Rachita Tygesen, Malin P Qvortrup, Klaus Kristiansen, Karsten Quistorff, Bjørn Gupta, Ramneek Wang, Jun Hansen, Jacob B BMC Genomics Research Article BACKGROUND: Large mammals are capable of thermoregulation shortly after birth due to the presence of brown adipose tissue (BAT). The majority of BAT disappears after birth and is replaced by white adipose tissue (WAT). RESULTS: We analyzed the postnatal transformation of adipose in sheep with a time course study of the perirenal adipose depot. We observed changes in tissue morphology, gene expression and metabolism within the first two weeks of postnatal life consistent with the expected transition from BAT to WAT. The transformation was characterized by massively decreased mitochondrial abundance and down-regulation of gene expression related to mitochondrial function and oxidative phosphorylation. Global gene expression profiling demonstrated that the time points grouped into three phases: a brown adipose phase, a transition phase and a white adipose phase. Between the brown adipose and the transition phase 170 genes were differentially expressed, and 717 genes were differentially expressed between the transition and the white adipose phase. Thirty-eight genes were shared among the two sets of differentially expressed genes. We identified a number of regulated transcription factors, including NR1H3, MYC, KLF4, ESR1, RELA and BCL6, which were linked to the overall changes in gene expression during the adipose tissue remodeling. Finally, the perirenal adipose tissue expressed both brown and brite/beige adipocyte marker genes at birth, the expression of which changed substantially over time. CONCLUSIONS: Using global gene expression profiling of the postnatal BAT to WAT transformation in sheep, we provide novel insight into adipose tissue plasticity in a large mammal, including identification of novel transcriptional components linked to adipose tissue remodeling. Moreover, our data set provides a useful resource for further studies in adipose tissue plasticity. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-1405-8) contains supplementary material, which is available to authorized users. BioMed Central 2015-03-19 /pmc/articles/PMC4407871/ /pubmed/25887780 http://dx.doi.org/10.1186/s12864-015-1405-8 Text en © Basse et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Basse, Astrid L
Dixen, Karen
Yadav, Rachita
Tygesen, Malin P
Qvortrup, Klaus
Kristiansen, Karsten
Quistorff, Bjørn
Gupta, Ramneek
Wang, Jun
Hansen, Jacob B
Global gene expression profiling of brown to white adipose tissue transformation in sheep reveals novel transcriptional components linked to adipose remodeling
title Global gene expression profiling of brown to white adipose tissue transformation in sheep reveals novel transcriptional components linked to adipose remodeling
title_full Global gene expression profiling of brown to white adipose tissue transformation in sheep reveals novel transcriptional components linked to adipose remodeling
title_fullStr Global gene expression profiling of brown to white adipose tissue transformation in sheep reveals novel transcriptional components linked to adipose remodeling
title_full_unstemmed Global gene expression profiling of brown to white adipose tissue transformation in sheep reveals novel transcriptional components linked to adipose remodeling
title_short Global gene expression profiling of brown to white adipose tissue transformation in sheep reveals novel transcriptional components linked to adipose remodeling
title_sort global gene expression profiling of brown to white adipose tissue transformation in sheep reveals novel transcriptional components linked to adipose remodeling
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4407871/
https://www.ncbi.nlm.nih.gov/pubmed/25887780
http://dx.doi.org/10.1186/s12864-015-1405-8
work_keys_str_mv AT basseastridl globalgeneexpressionprofilingofbrowntowhiteadiposetissuetransformationinsheeprevealsnoveltranscriptionalcomponentslinkedtoadiposeremodeling
AT dixenkaren globalgeneexpressionprofilingofbrowntowhiteadiposetissuetransformationinsheeprevealsnoveltranscriptionalcomponentslinkedtoadiposeremodeling
AT yadavrachita globalgeneexpressionprofilingofbrowntowhiteadiposetissuetransformationinsheeprevealsnoveltranscriptionalcomponentslinkedtoadiposeremodeling
AT tygesenmalinp globalgeneexpressionprofilingofbrowntowhiteadiposetissuetransformationinsheeprevealsnoveltranscriptionalcomponentslinkedtoadiposeremodeling
AT qvortrupklaus globalgeneexpressionprofilingofbrowntowhiteadiposetissuetransformationinsheeprevealsnoveltranscriptionalcomponentslinkedtoadiposeremodeling
AT kristiansenkarsten globalgeneexpressionprofilingofbrowntowhiteadiposetissuetransformationinsheeprevealsnoveltranscriptionalcomponentslinkedtoadiposeremodeling
AT quistorffbjørn globalgeneexpressionprofilingofbrowntowhiteadiposetissuetransformationinsheeprevealsnoveltranscriptionalcomponentslinkedtoadiposeremodeling
AT guptaramneek globalgeneexpressionprofilingofbrowntowhiteadiposetissuetransformationinsheeprevealsnoveltranscriptionalcomponentslinkedtoadiposeremodeling
AT wangjun globalgeneexpressionprofilingofbrowntowhiteadiposetissuetransformationinsheeprevealsnoveltranscriptionalcomponentslinkedtoadiposeremodeling
AT hansenjacobb globalgeneexpressionprofilingofbrowntowhiteadiposetissuetransformationinsheeprevealsnoveltranscriptionalcomponentslinkedtoadiposeremodeling