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A Possible Inflammatory Role of Twist1 in Human White Adipocytes

OBJECTIVE: Twist1 is a transcription factor that is highly expressed in murine brown and white adipose tissue (WAT) and negatively regulates fatty acid oxidation in mice. The role of twist1 in WAT is not known and was therefore examined. RESEARCH DESIGN AND METHODS: The expression of twist1 was dete...

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Autores principales: Pettersson, Amanda T., Laurencikiene, Jurga, Mejhert, Niklas, Näslund, Erik, Bouloumié, Anne, Dahlman, Ingrid, Arner, Peter, Rydén, Mikael
Formato: Texto
Lenguaje:English
Publicado: American Diabetes Association 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2828644/
https://www.ncbi.nlm.nih.gov/pubmed/20007935
http://dx.doi.org/10.2337/db09-0997
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author Pettersson, Amanda T.
Laurencikiene, Jurga
Mejhert, Niklas
Näslund, Erik
Bouloumié, Anne
Dahlman, Ingrid
Arner, Peter
Rydén, Mikael
author_facet Pettersson, Amanda T.
Laurencikiene, Jurga
Mejhert, Niklas
Näslund, Erik
Bouloumié, Anne
Dahlman, Ingrid
Arner, Peter
Rydén, Mikael
author_sort Pettersson, Amanda T.
collection PubMed
description OBJECTIVE: Twist1 is a transcription factor that is highly expressed in murine brown and white adipose tissue (WAT) and negatively regulates fatty acid oxidation in mice. The role of twist1 in WAT is not known and was therefore examined. RESEARCH DESIGN AND METHODS: The expression of twist1 was determined by quantitative real-time PCR in different tissues and in different cell types within adipose tissue. The effect of twist1 small interfering RNA on fatty acid oxidation, lipolysis, adipokine secretion, and mRNA expression was determined in human adipocytes. The interaction between twist1 and specific promoters in human adipocytes was investigated by chromatin immunoprecipitation (ChIP) and reporter assays. RESULTS: Twist1 was highly expressed in human WAT compared with a set of other tissues and found predominantly in adipocytes. Twist1 levels increased during in vitro differentiation of human preadipocytes. Gene silencing of twist1 in human white adipocytes had no effect on lipolysis or glucose transport. Unexpectedly, and in contrast with results in mice, twist1 RNA interference reduced fatty acid oxidation. Furthermore, the expression and secretion of the inflammatory factors tumor necrosis factor-α, interleukin-6, and monocyte chemoattractant protein-1 were downregulated by twist1 silencing. ChIP and reporter assays confirmed twist1 interaction with the promoters of these genes. CONCLUSIONS: Twist1 may play a role in inflammation of human WAT because it can regulate the expression and secretion of inflammatory adipokines via direct transcriptional effects in white adipocytes. Furthermore, twist1 may, in contrast to findings in mice, be a positive regulator of fatty acid oxidation in human white adipocytes.
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spelling pubmed-28286442011-03-01 A Possible Inflammatory Role of Twist1 in Human White Adipocytes Pettersson, Amanda T. Laurencikiene, Jurga Mejhert, Niklas Näslund, Erik Bouloumié, Anne Dahlman, Ingrid Arner, Peter Rydén, Mikael Diabetes Original Article OBJECTIVE: Twist1 is a transcription factor that is highly expressed in murine brown and white adipose tissue (WAT) and negatively regulates fatty acid oxidation in mice. The role of twist1 in WAT is not known and was therefore examined. RESEARCH DESIGN AND METHODS: The expression of twist1 was determined by quantitative real-time PCR in different tissues and in different cell types within adipose tissue. The effect of twist1 small interfering RNA on fatty acid oxidation, lipolysis, adipokine secretion, and mRNA expression was determined in human adipocytes. The interaction between twist1 and specific promoters in human adipocytes was investigated by chromatin immunoprecipitation (ChIP) and reporter assays. RESULTS: Twist1 was highly expressed in human WAT compared with a set of other tissues and found predominantly in adipocytes. Twist1 levels increased during in vitro differentiation of human preadipocytes. Gene silencing of twist1 in human white adipocytes had no effect on lipolysis or glucose transport. Unexpectedly, and in contrast with results in mice, twist1 RNA interference reduced fatty acid oxidation. Furthermore, the expression and secretion of the inflammatory factors tumor necrosis factor-α, interleukin-6, and monocyte chemoattractant protein-1 were downregulated by twist1 silencing. ChIP and reporter assays confirmed twist1 interaction with the promoters of these genes. CONCLUSIONS: Twist1 may play a role in inflammation of human WAT because it can regulate the expression and secretion of inflammatory adipokines via direct transcriptional effects in white adipocytes. Furthermore, twist1 may, in contrast to findings in mice, be a positive regulator of fatty acid oxidation in human white adipocytes. American Diabetes Association 2010-03 2009-12-10 /pmc/articles/PMC2828644/ /pubmed/20007935 http://dx.doi.org/10.2337/db09-0997 Text en © 2010 by the American Diabetes Association. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details.
spellingShingle Original Article
Pettersson, Amanda T.
Laurencikiene, Jurga
Mejhert, Niklas
Näslund, Erik
Bouloumié, Anne
Dahlman, Ingrid
Arner, Peter
Rydén, Mikael
A Possible Inflammatory Role of Twist1 in Human White Adipocytes
title A Possible Inflammatory Role of Twist1 in Human White Adipocytes
title_full A Possible Inflammatory Role of Twist1 in Human White Adipocytes
title_fullStr A Possible Inflammatory Role of Twist1 in Human White Adipocytes
title_full_unstemmed A Possible Inflammatory Role of Twist1 in Human White Adipocytes
title_short A Possible Inflammatory Role of Twist1 in Human White Adipocytes
title_sort possible inflammatory role of twist1 in human white adipocytes
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2828644/
https://www.ncbi.nlm.nih.gov/pubmed/20007935
http://dx.doi.org/10.2337/db09-0997
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