The Nuclear Orphan Receptor COUP-TFII Plays an Essential Role in Adipogenesis, Glucose Homeostasis, and Energy Metabolism

被引:120
作者
Li, Luoping [1 ]
Xie, Xin [1 ]
Qin, Jun [1 ]
Jeha, George S. [1 ]
Saha, Pradip K. [1 ,2 ]
Yan, Jun [1 ]
Haueter, Claire M. [3 ]
Chan, Lawrence [1 ,2 ]
Tsai, Sophia Y. [1 ,2 ,4 ]
Tsai, Ming-Jer [1 ,2 ,4 ]
机构
[1] Baylor Coll Med, Dept Mol & Cellular Biol, Houston, TX 77030 USA
[2] Baylor Coll Med, Dept Med, Houston, TX 77030 USA
[3] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
[4] Baylor Coll Med, Program Dev Biol, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
TRANSCRIPTION FACTOR-II; INSULIN-RESISTANCE; OBESITY; MUSCLE; MICE;
D O I
10.1016/j.cmet.2008.12.002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Adipose tissue development and function play a central role in the pathogenesis and pathophysiology of metabolic syndromes. Here, we show that chicken ovalbumin upstream promoter transcription factor II (COUP-TFII) plays a pivotal role in adipogenesis and energy homeostasis. COUP-TFII is expressed in the early stages of white adipocyte development. COUP-TFII heterozygous mice (COUP-TFII+/-) have much less white adipose tissue (WAT) than wild-type mice (COUP-TFII+/+). COUP-TFII+/- mice display a decreased expression of key regulators for WAT development. Knockdown COUP-TFII in 3T3-L1 cells resulted in an increased expression of Wnt10b, while chromatin immunoprecipitation analysis revealed that Wnt10b is a direct target of COUP-TFII. Moreover, COUP-TFII+/- mice have increased mitochondrial biogenesis in WAT, and COUP-TFII+/- mice have improved glucose homeostasis and increased energy expenditure. Thus, COUP-TFII regulates adipogenesis by regulating the key molecules in adipocyte development and can serve as a target for regulating energy metabolism.
引用
收藏
页码:77 / 87
页数:11
相关论文
共 23 条
[1]   CELLULAR AND MOLECULAR ASPECTS OF ADIPOSE-TISSUE DEVELOPMENT [J].
AILHAUD, G ;
GRIMALDI, P ;
NEGREL, R .
ANNUAL REVIEW OF NUTRITION, 1992, 12 :207-233
[2]   From mice to men: Insights into the insulin resistance syndromes [J].
Biddinger, SB ;
Kahn, CR .
ANNUAL REVIEW OF PHYSIOLOGY, 2006, 68 :123-158
[3]   Complete rescue of obesity, diabetes, and infertility in db/db mice by neuron-specific LEPR-B transgenes [J].
de Luca, C ;
Kowalski, TJ ;
Zhang, YY ;
Elmquist, JK ;
Lee, C ;
Kilimann, MW ;
Ludwig, T ;
Liu, SM ;
Chua, SC .
JOURNAL OF CLINICAL INVESTIGATION, 2005, 115 (12) :3484-3493
[4]   Transcriptional control of adipocyte formation [J].
Farmer, Stephen R. .
CELL METABOLISM, 2006, 4 (04) :263-273
[5]   A nuclear receptor atlas: 3T3-L1 adipogenesis [J].
Fu, MG ;
Sun, TW ;
Bookout, AL ;
Downes, M ;
Yu, RT ;
Evans, RM ;
Mangelsdorf, DJ .
MOLECULAR ENDOCRINOLOGY, 2005, 19 (10) :2437-2450
[6]  
HOSHIZAKI DK, 1994, DEVELOPMENT, V120, P2489
[7]   The role of lipid accumulation in liver and muscle for insulin resistance and type 2 diabetes mellitus in humans [J].
Krssak, M ;
Roden, M .
REVIEWS IN ENDOCRINE & METABOLIC DISORDERS, 2004, 5 (02) :127-134
[8]   COUP-TFII mediates progesterone regulation of uterine implantation by controlling ER activity [J].
Kurihara, Isao ;
Lee, Dong-Kee ;
Petit, Fabrice G. ;
Jeong, Jaewook ;
Lee, Kevin ;
Lydon, John P. ;
DeMayo, Francesco J. ;
Tsai, Ming-Jer ;
Tsai, Sophia Y. .
PLOS GENETICS, 2007, 3 (06) :1053-1064
[9]   The nuclear orphan receptor COUP-TFII is required for limb and skeletal muscle development [J].
Lee, CT ;
Li, LP ;
Takamoto, N ;
Martin, JF ;
DeMayo, FJ ;
Tsai, MJ ;
Tsai, SY .
MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (24) :10835-10843
[10]   Peroxisome-proliferator-activated receptor γ suppresses Wnt/β-catenin signalling during adipogenesis [J].
Moldes, M ;
Zuo, Y ;
Morrison, RF ;
Silva, D ;
Park, BH ;
Liu, JJ ;
Farmer, SR .
BIOCHEMICAL JOURNAL, 2003, 376 :607-613