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PPARs in the Control of Uncoupling Proteins Gene Expression

Uncoupling proteins (UCPs) are mitochondrial membrane transporters involved in the control of energy conversion in mitochondria. Experimental and genetic evidence relate dysfunctions of UCPs with metabolic syndrome and obesity. The PPAR subtypes mediate to a large extent the transcriptional regulati...

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Detalles Bibliográficos
Autores principales: Villarroya, Francesc, Iglesias, Roser, Giralt, Marta
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1779581/
https://www.ncbi.nlm.nih.gov/pubmed/17389766
http://dx.doi.org/10.1155/2007/74364
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author Villarroya, Francesc
Iglesias, Roser
Giralt, Marta
author_facet Villarroya, Francesc
Iglesias, Roser
Giralt, Marta
author_sort Villarroya, Francesc
collection PubMed
description Uncoupling proteins (UCPs) are mitochondrial membrane transporters involved in the control of energy conversion in mitochondria. Experimental and genetic evidence relate dysfunctions of UCPs with metabolic syndrome and obesity. The PPAR subtypes mediate to a large extent the transcriptional regulation of the UCP genes, with a distinct relevance depending on the UCP gene and the tissue in which it is expressed. UCP1 gene is under the dual control of PPARγ and PPARα in relation to brown adipocyte differentiation and lipid oxidation, respectively. UCP3 gene is regulated by PPARα and PPARδ in the muscle, heart, and adipose tissues. UCP2 gene is also under the control of PPARs even in tissues in which it is the predominantly expressed UCP (eg, the pancreas and liver). This review summarizes the current understanding of the role of PPARs in UCPs gene expression in normal conditions and also in the context of type-2 diabetes or obesity.
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spelling pubmed-17795812007-02-01 PPARs in the Control of Uncoupling Proteins Gene Expression Villarroya, Francesc Iglesias, Roser Giralt, Marta PPAR Res Review Article Uncoupling proteins (UCPs) are mitochondrial membrane transporters involved in the control of energy conversion in mitochondria. Experimental and genetic evidence relate dysfunctions of UCPs with metabolic syndrome and obesity. The PPAR subtypes mediate to a large extent the transcriptional regulation of the UCP genes, with a distinct relevance depending on the UCP gene and the tissue in which it is expressed. UCP1 gene is under the dual control of PPARγ and PPARα in relation to brown adipocyte differentiation and lipid oxidation, respectively. UCP3 gene is regulated by PPARα and PPARδ in the muscle, heart, and adipose tissues. UCP2 gene is also under the control of PPARs even in tissues in which it is the predominantly expressed UCP (eg, the pancreas and liver). This review summarizes the current understanding of the role of PPARs in UCPs gene expression in normal conditions and also in the context of type-2 diabetes or obesity. Hindawi Publishing Corporation 2007 2006-11-28 /pmc/articles/PMC1779581/ /pubmed/17389766 http://dx.doi.org/10.1155/2007/74364 Text en Copyright © 2007 Francesc Villarroya 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 Review Article
Villarroya, Francesc
Iglesias, Roser
Giralt, Marta
PPARs in the Control of Uncoupling Proteins Gene Expression
title PPARs in the Control of Uncoupling Proteins Gene Expression
title_full PPARs in the Control of Uncoupling Proteins Gene Expression
title_fullStr PPARs in the Control of Uncoupling Proteins Gene Expression
title_full_unstemmed PPARs in the Control of Uncoupling Proteins Gene Expression
title_short PPARs in the Control of Uncoupling Proteins Gene Expression
title_sort ppars in the control of uncoupling proteins gene expression
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1779581/
https://www.ncbi.nlm.nih.gov/pubmed/17389766
http://dx.doi.org/10.1155/2007/74364
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