Plac8 Is an Inducer of C/EBPβ Required for Brown Fat Differentiation, Thermoregulation, and Control of Body Weight

被引:92
作者
Jimenez-Preitner, Maria [1 ]
Berney, Xavier [1 ]
Uldry, Marc [1 ]
Vitali, Alessandra [2 ]
Cinti, Saverio [2 ]
Ledford, Julie G. [3 ]
Thorens, Bernard [1 ]
机构
[1] Univ Lausanne, Ctr Integrat Genom, CH-1015 Lausanne, Switzerland
[2] Univ Ancona, Fac Med, Dept Mol Pathol & Innovat Therapies, IT-60020 Ancona, Italy
[3] Duke Univ, Med Ctr, Durham, NC 27710 USA
基金
瑞士国家科学基金会;
关键词
BINDING-PROTEIN-BETA; ADIPOSE-TISSUE; TRANSCRIPTIONAL CONTROL; ADIPOCYTE DIFFERENTIATION; MICE LACKING; ONZIN; ADIPOGENESIS; EXPRESSION; TARGET; GENES;
D O I
10.1016/j.cmet.2011.08.008
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Brown adipocytes oxidize fatty acids to produce heat in response to cold or to excessive energy intake; stimulation of brown fat development and function may thus counteract obesity. Brown adipogenesis requires activation of the transcription factor C/EBP beta and recruitment of the zinc finger protein Prdm16, but upstream inducers of these proteins are incompletely defined. Here, we show that genetic inactivation of Plac8, a gene encoding an evolutionarily conserved protein, induces cold intolerance, and late-onset obesity, as well as abnormal morphology and impaired function of brown adipocytes. Using brown preadipocyte lines we show that Plac8 is required for brown fat differentiation, that its overexpression induces C/EBP beta and Prdm16, and that upon induction of differentiation Plac8 associates with C/EBP beta and binds to the C/EBP beta promoter to induce its transcription. Thus, Plac8 is a critical upstream regulator of brown fat differentiation and function that acts, at least in part, by inducing C/EBP beta expression.
引用
收藏
页码:658 / 670
页数:13
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