首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >The ubiquitin ligase Fbxw7 controls adipocyte differentiation by targeting C/EBPα for degradation
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The ubiquitin ligase Fbxw7 controls adipocyte differentiation by targeting C/EBPα for degradation

机译:泛素连接酶Fbxw7通过靶向C /EBPα降解来控制脂肪细胞分化

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摘要

Adipose tissue controls body lipid and energy metabolism, as well as food intake, and abnormalities in adipose function play a central role in diseases such as obesity and type-2 diabetes. Adipocyte differentiation is controlled by a transcriptional cascade involving PPARγ and members of the C/EBP family of transcription factors. Here, we demonstrate that C/EBPα is targeted for degradation by the ubiquitin ligase Fbxw7 in a phosphorylation-dependent manner. Importantly, inactivation of Fbxw7 is sufficient to convert mouse preadipocytes into mature adipocytes in a manner dependent on C/EBPα. In addition, inactivation of Fbxw7 promotes adipocyte differentiation of human adult stem cells. Taken together, our results suggest that Fbxw7 is a negative regulator of adipogenesis by targeting C/EBPα for degradation. This notion is supported by the observation that the expression of Fbxw7 is down-regulated during adipocyte differentiation, resulting in the accumulation of proadipogenic proteins such as C/EBPα. Thus, Fbxw7 could be an important regulator of energy and lipid metabolism.
机译:脂肪组织控制着人体的脂质和能量代谢以及食物摄入,而脂肪功能异常在诸如肥胖症和2型糖尿病等疾病中起着核心作用。脂肪细胞的分化是由涉及PPARγ和转录因子C / EBP家族成员的转录级联控制的。在这里,我们证明了C /EBPα被磷酸化依赖性方式的遍在蛋白连接酶Fbxw7降解。重要的是,Fbxw7的失活足以以依赖C /EBPα的方式将小鼠前脂肪细胞转化为成熟脂肪细胞。此外,Fbxw7的失活促进了成人干细胞的脂肪细胞分化。两者合计,我们的结果表明Fbxw7通过靶向C /EBPα降解是脂肪生成的负调节剂。 Fbxw7的表达在脂肪细胞分化过程中被下调,导致促脂肪原性蛋白质(例如C /EBPα)的积累,支持了这一观点。因此,Fbxw7可能是能量和脂质代谢的重要调节剂。

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