AQP1- A regulatory factor associated with brown adipose tissue-silencing to combat obesity and metabolic disease.

IF 3.1 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Chloe Cheng, Christopher Blay, Pei-Yin Tsai, Muying Li, Matthew Williams, Noel Acor, Kaydine Edwards, Yue Qu, Yang Liu, Leah D'Silva, Nina Buettner, Claire Walter, Mary Snyder, Ines Pd Costa, Olivier Devuyst, Joeva Barrow
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引用次数: 0

Abstract

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.

AQP1-一种与棕色脂肪组织沉默相关的调节因子,可对抗肥胖和代谢疾病。
在面对饮食性肥胖(DIO)时,环境冷刺激激活棕色脂肪组织(BAT)中的非寒战产热(NST)产生了强大的代谢益处。然而,利用棕色脂肪NST治疗代谢性疾病的一个关键障碍是,BAT在人体生理环境温度条件下是沉默的和不活跃的。控制这种沉默过程的机制仍然知之甚少。在这里,我们通过蛋白质组学分析在野生型(WT)小鼠的棕色脂肪中发现了一个假定的蝙蝠沉默因子,水通道蛋白-1 (AQP1)。我们培育了第一个BAT特异性AQP1敲除小鼠(AQP1- ko),发现AQP1- ko可以在BAT沉默环境条件下激活NST,并且与Flox对照相比,AQP1- ko小鼠对DIO和代谢功能障碍有显著保护。我们发现,与Flox对照小鼠相比,高脂肪饮食(HFD)的AQP1-KO小鼠通过减少脂肪量、改善葡萄糖耐量和增加全身能量消耗来减少体重增加。从机制上讲,我们发现在BAT环境沉默条件下,小鼠AQP1消融可以上调与电子传递链(ETC)和线粒体翻译相关的基因表达,从而激活NST。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
9.80
自引率
0.00%
发文量
98
审稿时长
1 months
期刊介绍: The American Journal of Physiology-Endocrinology and Metabolism publishes original, mechanistic studies on the physiology of endocrine and metabolic systems. Physiological, cellular, and molecular studies in whole animals or humans will be considered. Specific themes include, but are not limited to, mechanisms of hormone and growth factor action; hormonal and nutritional regulation of metabolism, inflammation, microbiome and energy balance; integrative organ cross talk; paracrine and autocrine control of endocrine cells; function and activation of hormone receptors; endocrine or metabolic control of channels, transporters, and membrane function; temporal analysis of hormone secretion and metabolism; and mathematical/kinetic modeling of metabolism. Novel molecular, immunological, or biophysical studies of hormone action are also welcome.
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