Literature DB >> 17272390

A novel inhibitory protein in adipose tissue, the aldo-keto reductase AKR1B7: its role in adipogenesis.

Julien Tirard1, Johann Gout, Anne Marie Lefrançois-Martinez, Antoine Martinez, Martine Begeot, Danielle Naville.   

Abstract

The aldo-keto reductase 1B7 (AKR1B7) encodes an aldose-reductase that has been reported as a detoxification enzyme until now. We have demonstrated that AKR1B7 is differently expressed in various mouse white adipose tissues depending on their location. Its expression is associated with a higher ratio of preadipocytes vs. adipocytes. The cells that express AKR1B7 did not contain lipid droplets, and the expression level of akr1b7 was very low in mature adipocytes. We have defined the role of AKR1B7 in adipogenesis using either primary cultures of adipose stromal cells (containing adipocyte precursors) or the 3T3-L1 cell line. Under the same differentiation conditions, adipose stromal cells from tissues that expressed AKR1B7 had a decreased capacity to accumulate lipids compared with those that did not express it. Moreover, the overexpression of sense or antisense AKR1B7 in 3T3-L1 preadipocytes inhibited or accelerated, respectively, their rate of differentiation into adipocytes. In vivo experiments demonstrated that AKR1B7-encoding mRNA expression decreased in adipose tissues from mice where obesity was induced by a high-fat diet. All these results attributed for the first time a novel role to AKR1B7, which is the inhibition of adipogenesis in some adipose tissues.

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Year:  2007        PMID: 17272390     DOI: 10.1210/en.2006-1707

Source DB:  PubMed          Journal:  Endocrinology        ISSN: 0013-7227            Impact factor:   4.736


  17 in total

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Journal:  Acta Endocrinol (Buchar)       Date:  2021 Apr-Jun       Impact factor: 0.877

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Authors:  Sharda P Singh; Maciej Niemczyk; Ludwika Zimniak; Piotr Zimniak
Journal:  Aging (Albany NY)       Date:  2008-12-18       Impact factor: 5.682

4.  Suppression of adipocyte differentiation by aldo-keto reductase 1B3 acting as prostaglandin F2alpha synthase.

Authors:  Ko Fujimori; Toshiyuki Ueno; Nanae Nagata; Kaori Kashiwagi; Kosuke Aritake; Fumio Amano; Yoshihiro Urade
Journal:  J Biol Chem       Date:  2010-01-21       Impact factor: 5.157

5.  The aldo-keto reductase Akr1b7 gene is a common transcriptional target of xenobiotic receptors pregnane X receptor and constitutive androstane receptor.

Authors:  Ming-Jie Liu; Yuki Takahashi; Taira Wada; Jinhan He; Jie Gao; Yanan Tian; Song Li; Wen Xie
Journal:  Mol Pharmacol       Date:  2009-06-19       Impact factor: 4.436

6.  Role of the pregnane X receptor in binge ethanol-induced steatosis and hepatotoxicity.

Authors:  Sora Choi; Afua A Gyamfi; Prince Neequaye; Samuel Addo; Frank J Gonzalez; Maxwell A Gyamfi
Journal:  J Pharmacol Exp Ther       Date:  2018-02-05       Impact factor: 4.030

7.  Aldo-Keto Reductases 1B in Endocrinology and Metabolism.

Authors:  Emilie Pastel; Jean-Christophe Pointud; Fanny Volat; Antoine Martinez; Anne-Marie Lefrançois-Martinez
Journal:  Front Pharmacol       Date:  2012-08-02       Impact factor: 5.810

8.  Aldo keto reductase 1B7 and prostaglandin F2alpha are regulators of adrenal endocrine functions.

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Journal:  PLoS One       Date:  2009-10-07       Impact factor: 3.240

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Authors:  Fanny E Volat; Jean-Christophe Pointud; Emilie Pastel; Béatrice Morio; Benoit Sion; Ghislaine Hamard; Michel Guichardant; Romain Colas; Anne-Marie Lefrançois-Martinez; Antoine Martinez
Journal:  Diabetes       Date:  2012-07-30       Impact factor: 9.461

10.  Prostaglandins as PPARγ Modulators in Adipogenesis.

Authors:  Ko Fujimori
Journal:  PPAR Res       Date:  2012-12-25       Impact factor: 4.964

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