White to Brown Fat Phenotypic Switch Induced by Genetic and Environmental Activation of a Hypothalamic-Adipocyte Axis

被引:318
作者
Cao, Lei [1 ,2 ,3 ]
Choi, Eugene Y. [1 ,2 ,3 ]
Liu, Xianglan [1 ,2 ,3 ]
Martin, Adam [1 ,2 ,3 ]
Wang, Chuansong [1 ,2 ,3 ]
Xu, Xiaohua [4 ]
During, Matthew J. [1 ,2 ,3 ]
机构
[1] Ohio State Univ, Dept Mol Virol Immunol & Med Genet, Coll Publ Hlth, Columbus, OH 43210 USA
[2] Ohio State Univ, Dept Neurosci, Coll Publ Hlth, Columbus, OH 43210 USA
[3] Ohio State Univ, Ctr Comprehens Canc, Coll Publ Hlth, Columbus, OH 43210 USA
[4] Ohio State Univ, Div Environm Hlth Sci, Coll Publ Hlth, Columbus, OH 43210 USA
基金
美国国家卫生研究院;
关键词
DIET-INDUCED THERMOGENESIS; REGULATES ENERGY-BALANCE; ADIPOSE-TISSUE; NEUROTROPHIC FACTOR; COLD-EXPOSURE; MICE LACKING; OBESITY; BRAIN; PROTEIN; INNERVATION;
D O I
10.1016/j.cmet.2011.06.020
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Living in an enriched environment with complex physical and social stimulation leads to improved cognitive and metabolic health. In white fat, enrichment induced the upregulation of the brown fat cell fate determining gene Prdm16, brown fat-specific markers, and genes involved in thermogenesis and beta-adrenergic signaling. Moreover, pockets of cells with prototypical brown fat morphology and high UCP1 levels were observed in the white fat of enriched mice associated with resistance to diet-induced obesity. Hypothalamic overexpression of BDNF reproduced the enrichment-associated activation of the brown fat gene program and lean phenotype. Inhibition of BDNF signaling by genetic knockout or dominant-negative trkB reversed this phenotype. Our genetic and pharmacologic data suggest a mechanism whereby induction of hypothalamic BDNF expression in response to environmental stimuli leads to selective sympathoneural modulation of white fat to induce "browning" and increased energy dissipation.
引用
收藏
页码:324 / 338
页数:15
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