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Reduced adiponectin expression after high-fat diet is associated with selective up-regulation of ALDH1A1 and further retinoic acid receptor signaling in adipose tissue

Adiponectin is an adipocyte-derived adipokine with potent antidiabetic, anti-inflammatory, and antiatherogenic activity. Long-term, high-fat diet results in gain of body weight, adiposity, further inflammatory-based cardiovascular diseases, and reduced adiponectin secretion. Vitamin A derivatives/re...

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Autores principales: Landrier, Jean-Francois, Kasiri, Elnaz, Karkeni, Esma, Mihály, Johanna, Béke, Gabriella, Weiss, Kathrin, Lucas, Renata, Aydemir, Gamze, Salles, Jérome, Walrand, Stéphane, de Lera, Angel R., Rühl, Ralph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Federation of American Societies for Experimental Biology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5161515/
https://www.ncbi.nlm.nih.gov/pubmed/27729412
http://dx.doi.org/10.1096/fj.201600263RR
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author Landrier, Jean-Francois
Kasiri, Elnaz
Karkeni, Esma
Mihály, Johanna
Béke, Gabriella
Weiss, Kathrin
Lucas, Renata
Aydemir, Gamze
Salles, Jérome
Walrand, Stéphane
de Lera, Angel R.
Rühl, Ralph
author_facet Landrier, Jean-Francois
Kasiri, Elnaz
Karkeni, Esma
Mihály, Johanna
Béke, Gabriella
Weiss, Kathrin
Lucas, Renata
Aydemir, Gamze
Salles, Jérome
Walrand, Stéphane
de Lera, Angel R.
Rühl, Ralph
author_sort Landrier, Jean-Francois
collection PubMed
description Adiponectin is an adipocyte-derived adipokine with potent antidiabetic, anti-inflammatory, and antiatherogenic activity. Long-term, high-fat diet results in gain of body weight, adiposity, further inflammatory-based cardiovascular diseases, and reduced adiponectin secretion. Vitamin A derivatives/retinoids are involved in several of these processes, which mainly take place in white adipose tissue (WAT). In this study, we examined adiponectin expression as a function of dietary high-fat and high–vitamin A conditions in mice. A decrease of adiponectin expression in addition to an up-regulation of aldehyde dehydrogenase A1 (ALDH1A1), retinoid signaling, and retinoic acid response element signaling was selectively observed in WAT of mice fed a normal–vitamin A, high-fat diet. Reduced adiponectin expression in WAT was also observed in mice fed a high–vitamin A diet. Adipocyte cell culture revealed that endogenous and synthetic retinoic acid receptor (RAR)α- and RARγ-selective agonists, as well as a synthetic retinoid X receptor agonist, efficiently reduced adiponectin expression, whereas ALDH1A1 expression only increased with RAR agonists. We conclude that reduced adiponectin expression under high-fat dietary conditions is dependent on 1) increased ALDH1A1 expression in adipocytes, which does not increase all-trans-retinoic acid levels; 2) further RAR ligand–induced, WAT-selective, increased retinoic acid response element–mediated signaling; and 3) RAR ligand–dependent reduction of adiponectin expression.—Landrier, J.-F., Kasiri, E., Karkeni, E., Mihály, J., Béke, G., Weiss, K., Lucas, R., Aydemir, G., Salles, J., Walrand, S., de Lera, A. R., Rühl, R. Reduced adiponectin expression after high-fat diet is associated with selective up-regulation of ALDH1A1 and further retinoic acid receptor signaling in adipose tissue.
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spelling pubmed-51615152016-12-19 Reduced adiponectin expression after high-fat diet is associated with selective up-regulation of ALDH1A1 and further retinoic acid receptor signaling in adipose tissue Landrier, Jean-Francois Kasiri, Elnaz Karkeni, Esma Mihály, Johanna Béke, Gabriella Weiss, Kathrin Lucas, Renata Aydemir, Gamze Salles, Jérome Walrand, Stéphane de Lera, Angel R. Rühl, Ralph FASEB J Research Adiponectin is an adipocyte-derived adipokine with potent antidiabetic, anti-inflammatory, and antiatherogenic activity. Long-term, high-fat diet results in gain of body weight, adiposity, further inflammatory-based cardiovascular diseases, and reduced adiponectin secretion. Vitamin A derivatives/retinoids are involved in several of these processes, which mainly take place in white adipose tissue (WAT). In this study, we examined adiponectin expression as a function of dietary high-fat and high–vitamin A conditions in mice. A decrease of adiponectin expression in addition to an up-regulation of aldehyde dehydrogenase A1 (ALDH1A1), retinoid signaling, and retinoic acid response element signaling was selectively observed in WAT of mice fed a normal–vitamin A, high-fat diet. Reduced adiponectin expression in WAT was also observed in mice fed a high–vitamin A diet. Adipocyte cell culture revealed that endogenous and synthetic retinoic acid receptor (RAR)α- and RARγ-selective agonists, as well as a synthetic retinoid X receptor agonist, efficiently reduced adiponectin expression, whereas ALDH1A1 expression only increased with RAR agonists. We conclude that reduced adiponectin expression under high-fat dietary conditions is dependent on 1) increased ALDH1A1 expression in adipocytes, which does not increase all-trans-retinoic acid levels; 2) further RAR ligand–induced, WAT-selective, increased retinoic acid response element–mediated signaling; and 3) RAR ligand–dependent reduction of adiponectin expression.—Landrier, J.-F., Kasiri, E., Karkeni, E., Mihály, J., Béke, G., Weiss, K., Lucas, R., Aydemir, G., Salles, J., Walrand, S., de Lera, A. R., Rühl, R. Reduced adiponectin expression after high-fat diet is associated with selective up-regulation of ALDH1A1 and further retinoic acid receptor signaling in adipose tissue. Federation of American Societies for Experimental Biology 2017-01 2016-10-11 /pmc/articles/PMC5161515/ /pubmed/27729412 http://dx.doi.org/10.1096/fj.201600263RR Text en © The Author(s) http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0) (http://creativecommons.org/licenses/by-nc/4.0/) which permits noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Landrier, Jean-Francois
Kasiri, Elnaz
Karkeni, Esma
Mihály, Johanna
Béke, Gabriella
Weiss, Kathrin
Lucas, Renata
Aydemir, Gamze
Salles, Jérome
Walrand, Stéphane
de Lera, Angel R.
Rühl, Ralph
Reduced adiponectin expression after high-fat diet is associated with selective up-regulation of ALDH1A1 and further retinoic acid receptor signaling in adipose tissue
title Reduced adiponectin expression after high-fat diet is associated with selective up-regulation of ALDH1A1 and further retinoic acid receptor signaling in adipose tissue
title_full Reduced adiponectin expression after high-fat diet is associated with selective up-regulation of ALDH1A1 and further retinoic acid receptor signaling in adipose tissue
title_fullStr Reduced adiponectin expression after high-fat diet is associated with selective up-regulation of ALDH1A1 and further retinoic acid receptor signaling in adipose tissue
title_full_unstemmed Reduced adiponectin expression after high-fat diet is associated with selective up-regulation of ALDH1A1 and further retinoic acid receptor signaling in adipose tissue
title_short Reduced adiponectin expression after high-fat diet is associated with selective up-regulation of ALDH1A1 and further retinoic acid receptor signaling in adipose tissue
title_sort reduced adiponectin expression after high-fat diet is associated with selective up-regulation of aldh1a1 and further retinoic acid receptor signaling in adipose tissue
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5161515/
https://www.ncbi.nlm.nih.gov/pubmed/27729412
http://dx.doi.org/10.1096/fj.201600263RR
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