Smad3 Deficiency in Mice Protects Against Insulin Resistance and Obesity Induced by a High-Fat Diet

被引:120
作者
Tan, Chek Kim [1 ]
Leuenberger, Nicolas [2 ]
Tan, Ming Jie [1 ]
Yan, Yew Wai [1 ]
Chen, Yinghui [1 ]
Kambadur, Ravi [1 ]
Wahli, Walter [2 ]
Tan, Nguan Soon [1 ]
机构
[1] Nanyang Technol Univ, Sch Biol Sci, Singapore, Singapore
[2] Univ Lausanne, Ctr Integrat Genom, Natl Res Ctr Frontiers Genet, Lausanne, Switzerland
基金
瑞士国家科学基金会;
关键词
GROWTH-FACTOR-BETA; ADIPOSE-TISSUE; TGF-BETA; METABOLIC SYNDROME; GENE-TRANSCRIPTION; LIPID-METABOLISM; SKELETAL-MUSCLE; PPAR-BETA/DELTA; LINKING OBESITY; ADIPOGENESIS;
D O I
10.2337/db10-0801
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE-Obesity and associated pathologies are major global health problems. Transforming growth factor-beta/Smad3 signaling has been implicated in various metabolic processes, including adipogenesis, insulin expression, and pancreatic beta-cell function. However, the systemic effects of Smad3 deficiency on adiposity and insulin resistance in vivo remain elusive. This study investigated the effects of Smad3 deficiency on whole-body glucose and lipid homeostasis and its contribution to the development of obesity and type 2 diabetes. RESEARCH DESIGN AND METHODS-We compared various metabolic profiles of Smad3-knockout and wild-type mice. We also determined the mechanism by which Smad3 deficiency affects the expression of genes involved in adipogenesis and metabolism. Mice were then challenged with a high-fat diet to study the impact of Smad3 deficiency on the development of obesity and insulin resistance. RESULTS-Smad3-knockout mice exhibited diminished adiposity with improved glucose tolerance and insulin sensitivity. Chromatin immunoprecipitation assay revealed that Smad3 deficiency increased CCAAT/enhancer-binding protein beta-C/EBP homologous protein 10 interaction and exerted a differential regulation on proliferator-activated receptor beta/delta and proliferator-activated receptor gamma expression in adipocytes. Focused gene expression profiling revealed an altered expression of genes involved in adipogenesis, lipid accumulation, and fatty acid beta-oxidation, indicative of altered adipose physiology. Despite reduced physical activity with no modification in food intake, these mutant mice were resistant to obesity and insulin resistance induced by a high-fat diet. CONCLUSIONS-Smad3 is a multifaceted regulator in adipose physiology and the pathogenesis of obesity and type 2 diabetes, suggesting that Smad3 may be a potential target for the treatment of obesity and its associated disorders. Diabetes 60:464-476, 2011
引用
收藏
页码:464 / 476
页数:13
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