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AgRP神经元中Stat3信号的激活促进运动活性。

Activation of Stat3 signaling in AgRP neurons promotes locomotor activity.

作者信息

Mesaros Andrea, Koralov Sergei B, Rother Eva, Wunderlich F Thomas, Ernst Marianne B, Barsh Gregory S, Rajewsky Klaus, Brüning Jens C

机构信息

Department of Mouse Genetics and Metabolism, Institute for Genetics, Center of Molecular Medicine Cologne, and Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases, University of Cologne, D-50674 Cologne, Germany.

出版信息

Cell Metab. 2008 Mar;7(3):236-48. doi: 10.1016/j.cmet.2008.01.007.

Abstract

Leptin, an adipocyte-derived hormone, acts on hypothalamic neurons located in the arcuate nucleus (ARC) of the hypothalamus to regulate energy homeostasis. One of the leptin-regulated neuronal subtypes in the ARC are agouti-related peptide (AgRP)-expressing neurons, which are involved in the regulation of food intake and are directly inhibited by leptin. Leptin activates the signal transducer and activator of transcription 3 (Stat3), but the role of Stat3 in the regulation of AgRP neurons is unclear. Here we show that mice expressing a constitutively active version of Stat3 selectively in AgRP neurons are lean and exhibit relative resistance to diet-induced obesity. Surprisingly, this phenotype arises from increased locomotor activity in the presence of unaltered AgRP expression. These data demonstrate that Stat3-dependent signaling in AgRP neurons in the ARC controls locomotor activity independently of AgRP regulation.

摘要

瘦素是一种由脂肪细胞分泌的激素,作用于位于下丘脑弓状核(ARC)的下丘脑神经元,以调节能量平衡。ARC中受瘦素调节的神经元亚型之一是表达刺鼠相关肽(AgRP)的神经元,它们参与食物摄入的调节,并直接受到瘦素的抑制。瘦素激活信号转导和转录激活因子3(Stat3),但Stat3在AgRP神经元调节中的作用尚不清楚。在这里,我们表明在AgRP神经元中选择性表达组成型活性Stat3的小鼠体型偏瘦,并且对饮食诱导的肥胖表现出相对抗性。令人惊讶的是,这种表型源于在AgRP表达未改变的情况下运动活性增加。这些数据表明,ARC中AgRP神经元中依赖Stat3的信号传导独立于AgRP调节来控制运动活性。

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