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干细胞因子/Kit 信号通路调节线粒体功能和能量消耗。

The stem cell factor/Kit signalling pathway regulates mitochondrial function and energy expenditure.

机构信息

1] MOE Key Laboratory of Model Animal for Disease Study, Model Animal Research Center, Nanjing University, Nanjing, Jiangsu 210061, China [2].

1] MOE Key Laboratory of Model Animal for Disease Study, Model Animal Research Center, Nanjing University, Nanjing, Jiangsu 210061, China [2] Section of Comparative Medicine, Yale University School of Medicine, PO BOX 208016, New Haven, Connecticut 06520-8016, USA [3].

出版信息

Nat Commun. 2014 Jul 7;5:4282. doi: 10.1038/ncomms5282.

Abstract

Cell growth is tightly coupled with mitochondrial biogenesis in order to maintain energy and organelle homeostasis. Receptor tyrosine kinase Kit and its ligand, stem cell factor (SCF), play a critical role in the growth and survival of multiple cell lineages. Here we report that the expression of SCF and Kit in adipose tissues is responsive to food availability and environmental temperature, and is altered in obese mice and human patients. Mice carrying a loss-of-function mutation in Kit develop obesity as a result of decreased energy expenditure. These phenotypes are associated with reduced PGC-1α expression and mitochondrial dysfunction in brown adipose tissue and skeletal muscle. We further demonstrate that SCF/Kit directly promotes Ppargc1a transcription and mitochondrial biogenesis. Blocking Kit signalling in mice decreases PGC-1α expression and thermogenesis, while overexpressing SCF systemically or specifically in brown adipose tissue increases thermogenesis and reduces weight gain. Collectively, these data provide mechanistic insight into the regulation of mitochondrial function by SCF/Kit signalling and lay a foundation for exploring SCF/Kit signalling as a therapeutic target for metabolic diseases.

摘要

细胞生长与线粒体生物发生紧密偶联,以维持能量和细胞器的平衡。受体酪氨酸激酶 Kit 和它的配体干细胞因子(SCF)在多种细胞谱系的生长和存活中起着关键作用。在这里,我们报告说,脂肪组织中 SCF 和 Kit 的表达对食物供应和环境温度有反应,并在肥胖小鼠和人类患者中发生改变。携带 Kit 功能丧失突变的小鼠由于能量消耗减少而发展为肥胖。这些表型与棕色脂肪组织和骨骼肌中 PGC-1α 表达减少和线粒体功能障碍有关。我们进一步证明,SCF/Kit 可直接促进 Ppargc1a 转录和线粒体生物发生。在小鼠中阻断 Kit 信号会降低 PGC-1α 的表达和产热,而全身性或特异性地在棕色脂肪组织中过表达 SCF 会增加产热并减少体重增加。总的来说,这些数据为 SCF/Kit 信号调节线粒体功能提供了机制上的见解,并为探索 SCF/Kit 信号作为代谢疾病的治疗靶点奠定了基础。

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