Retinoic Acid Upregulates Preadipocyte Genes to Block Adipogenesis and Suppress Diet-Induced Obesity

被引:170
作者
Berry, Daniel C. [1 ,2 ]
DeSantis, David [2 ]
Soltanian, Hooman [3 ]
Croniger, Colleen M. [2 ]
Noy, Noa [1 ,2 ]
机构
[1] Case Western Reserve Univ, Sch Med, Dept Pharmacol, Cleveland, OH 44106 USA
[2] Case Western Reserve Univ, Sch Med, Dept Nutr, Cleveland, OH USA
[3] Case Med Ctr, Dept Plast Surg, Cleveland, OH USA
基金
美国国家卫生研究院;
关键词
BINDING PROTEIN-II; INHIBIT ADIPOCYTE DIFFERENTIATION; ACUTE PROMYELOCYTIC LEUKEMIA; ACTIVATED-RECEPTOR-GAMMA; CARCINOMA-CELL-GROWTH; TRANSCRIPTION FACTOR; ADIPOSE CONVERSION; INSULIN-RESISTANCE; PPAR-BETA/DELTA; PHASE-I;
D O I
10.2337/db11-1620
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Retinoic acid (RA) protects mice from diet-induced obesity. The activity is mediated in part through activation of the nuclear receptors RA receptors (RARs) and peroxisome proliferator activated receptor beta/delta and their associated binding proteins cellular RA binding protein type II (CRABP-II) and fatty acid binding protein type 5 in adipocytes and skeletal muscle, leading to enhanced lipid oxidation and energy dissipation. It was also reported that RA inhibits differentiation of cultured preadipocytes. However, whether the hormone suppresses adipogenesis in vivo and how the activity is propagated remained unknown. In this study, we show that RA inhibits adipocyte differentiation by activating the CRABP-II/RAR gamma path in preadipose cells, thereby upregulating the expression of the adipogenesis inhibitors Pref-1, Sox9, and Kruppel-like factor 2 (KLF2). In turn, KLF2 induces the expression of CRABP-II and RAR gamma, further potentiating inhibition of adipocyte differentiation by RA. The data also indicate that RA suppresses adipogenesis in vivo and that the activity significantly contributes to the ability of the hormone to counteract diet-induced obesity. Diabetes 61:1112-1121, 2012
引用
收藏
页码:1112 / 1121
页数:10
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