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WISP1/CCN4 inhibits adipocyte differentiation through repression of PPARγ activity

WISP1 (Wnt1-inducible signaling pathway protein-1, also known as CCN4) is a member of the CCN family able to mediate cell growth, transformation and survival in a tissue-specific manner. Here, we report that WISP1 expression was highly increased in preadipocytes and decreased during adipocyte differ...

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Autores principales: Ferrand, Nathalie, Béreziat, Véronique, Moldes, Marthe, Zaoui, Maurice, Larsen, Annette K., Sabbah, Michèle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5431985/
https://www.ncbi.nlm.nih.gov/pubmed/28496206
http://dx.doi.org/10.1038/s41598-017-01866-2
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author Ferrand, Nathalie
Béreziat, Véronique
Moldes, Marthe
Zaoui, Maurice
Larsen, Annette K.
Sabbah, Michèle
author_facet Ferrand, Nathalie
Béreziat, Véronique
Moldes, Marthe
Zaoui, Maurice
Larsen, Annette K.
Sabbah, Michèle
author_sort Ferrand, Nathalie
collection PubMed
description WISP1 (Wnt1-inducible signaling pathway protein-1, also known as CCN4) is a member of the CCN family able to mediate cell growth, transformation and survival in a tissue-specific manner. Here, we report that WISP1 expression was highly increased in preadipocytes and decreased during adipocyte differentiation. Moreover, we observed an increase in WISP1 gene expression in adipose tissue from both diet-induced and leptin-deficient ob/ob obese mice, suggesting that WISP1 could be involved in the pathophysiological onset of obesity. Interestingly, overexpression of WISP1 in 3T3-F442A cells prevented adipocyte differentiation via downregulation of peroxisome proliferator-activated receptor (PPARγ) transcriptional activity thereby attenuating the expression of adipogenic markers. Conversely, silencing of WISP1 enhanced adipocyte differentiation. We further show that the inactivation of PPARγ transcriptional activity was mediated, at least in part, by a direct physical association between WISP1 and PPARγ, followed by proteasome-dependent degradation of PPARγ. These results suggest for the first time that WISP1 interacts with PPARγ and that this interaction results in the inhibition of PPARγ activity. Taken together our results suggest that WISP1 functions as a negative regulator of adipogenesis.
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spelling pubmed-54319852017-05-16 WISP1/CCN4 inhibits adipocyte differentiation through repression of PPARγ activity Ferrand, Nathalie Béreziat, Véronique Moldes, Marthe Zaoui, Maurice Larsen, Annette K. Sabbah, Michèle Sci Rep Article WISP1 (Wnt1-inducible signaling pathway protein-1, also known as CCN4) is a member of the CCN family able to mediate cell growth, transformation and survival in a tissue-specific manner. Here, we report that WISP1 expression was highly increased in preadipocytes and decreased during adipocyte differentiation. Moreover, we observed an increase in WISP1 gene expression in adipose tissue from both diet-induced and leptin-deficient ob/ob obese mice, suggesting that WISP1 could be involved in the pathophysiological onset of obesity. Interestingly, overexpression of WISP1 in 3T3-F442A cells prevented adipocyte differentiation via downregulation of peroxisome proliferator-activated receptor (PPARγ) transcriptional activity thereby attenuating the expression of adipogenic markers. Conversely, silencing of WISP1 enhanced adipocyte differentiation. We further show that the inactivation of PPARγ transcriptional activity was mediated, at least in part, by a direct physical association between WISP1 and PPARγ, followed by proteasome-dependent degradation of PPARγ. These results suggest for the first time that WISP1 interacts with PPARγ and that this interaction results in the inhibition of PPARγ activity. Taken together our results suggest that WISP1 functions as a negative regulator of adipogenesis. Nature Publishing Group UK 2017-05-11 /pmc/articles/PMC5431985/ /pubmed/28496206 http://dx.doi.org/10.1038/s41598-017-01866-2 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Ferrand, Nathalie
Béreziat, Véronique
Moldes, Marthe
Zaoui, Maurice
Larsen, Annette K.
Sabbah, Michèle
WISP1/CCN4 inhibits adipocyte differentiation through repression of PPARγ activity
title WISP1/CCN4 inhibits adipocyte differentiation through repression of PPARγ activity
title_full WISP1/CCN4 inhibits adipocyte differentiation through repression of PPARγ activity
title_fullStr WISP1/CCN4 inhibits adipocyte differentiation through repression of PPARγ activity
title_full_unstemmed WISP1/CCN4 inhibits adipocyte differentiation through repression of PPARγ activity
title_short WISP1/CCN4 inhibits adipocyte differentiation through repression of PPARγ activity
title_sort wisp1/ccn4 inhibits adipocyte differentiation through repression of pparγ activity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5431985/
https://www.ncbi.nlm.nih.gov/pubmed/28496206
http://dx.doi.org/10.1038/s41598-017-01866-2
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