| Literature DB >> 24999927 |
Zan Huang1, Hai-Bin Ruan2, Li Xian3, Weiqian Chen3, Shujun Jiang3, Anying Song3, Qinghua Wang3, Peiliang Shi3, Xingxing Gu4, Xiang Gao3.
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.Entities:
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Year: 2014 PMID: 24999927 DOI: 10.1038/ncomms5282
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919