褐色脂肪组织
基因沉默
生物
内分泌学
脂肪组织
内科学
产热
细胞生物学
基因
医学
遗传学
作者
Chloe Cheng,Christopher Blay,Pei-Yin Tsai,Muying Li,Matthew Williams,Noel Acor,Kaydine Edwards,Yang Liu,Lindsay D’Silva,Nina Buettner,Claire Walter,Mary Snyder,Inês P. D. Costa,Olivier Devuyst,Joeva J. Barrow
出处
期刊:American Journal of Physiology-endocrinology and Metabolism
[American Physiological Society]
日期:2025-09-22
被引量:1
标识
DOI:10.1152/ajpendo.00380.2024
摘要
The activation of non-shivering thermogenesis (NST) in brown adipose tissue (BAT) by environmental cold challenge yields strong metabolic benefit in the face of diet-induced obesity (DIO). Yet, a critical barrier to leveraging brown fat NST for therapeutic use against metabolic disease is that BAT is silenced and inactive at physiological ambient temperature conditions in humans. The mechanisms that govern this silencing process remain poorly understood. Here, we identified a putative BAT-silencing factor, aquaporin-1 (AQP1), in brown fat from wild-type (WT) mice via proteomics analysis. We generated the first BAT-specific AQP1 knockout mice (AQP1-KO) and revealed that AQP1-KO could activate NST under BAT silencing environmental conditions and that the AQP1-KO mice were significantly protected against DIO and metabolic dysfunction compared to Flox controls. We found that AQP1-KO mice on high fat diet (HFD) had reduced weight gain through reductions in fat mass, improved glucose tolerance, and increased whole body energy expenditure compared to Flox control mice. Mechanistically, we show that AQP1 ablation in mice had upregulated gene expression related to the electron transport chain (ETC) and mitochondrial translation contributing to the activation of NST under BAT environmental silenced conditions.
科研通智能强力驱动
Strongly Powered by AbleSci AI