Lee Aileen H, Orliaguet Lucie, Youm Yun-Hee, Maeda Rae, Dlugos Tamara, Lei Yuanjiu, Coman Daniel, Shchukina Irina, Andhey Sairam, Smith Steven R, Ravussin Eric, Stadler Krisztian, Hyder Fahmeed, Artyomov Maxim N, Sugiura Yuki, Dixit Vishwa Deep
Department of Pathology, Yale School of Medicine, New Haven, CT 06520, USA.
Department of Comparative Medicine, Yale School of Medicine, New Haven, CT 06520, USA.
bioRxiv. 2024 Aug 8:2024.08.06.606880. doi: 10.1101/2024.08.06.606880.
Dietary interventions such as caloric restriction (CR) and methionine restriction that prolong lifespan induce the 'browning' of white adipose tissue (WAT), an adaptive metabolic response that increases heat production to maintain health. However, how diet influences adipose browning and metabolic health is unclear. Here, we identified that weight-loss induced by CR in humans reduces cysteine concentration in WAT suggesting depletion of this amino-acid may be involved in metabolic benefits of CR. To investigate the role of cysteine on organismal metabolism, we created a cysteine-deficiency mouse model in which dietary cysteine was eliminated and cystathionine γ-lyase (CTH), the enzyme that synthesizes cysteine was conditionally deleted. Using this animal model, we found that systemic cysteine-depletion causes drastic weight-loss with increased fat utilization and browning of adipose tissue. The restoration of dietary cysteine in cysteine-deficient mice rescued weight loss together with reversal of adipose browning and increased food-intake in an on-demand fashion. Mechanistically, cysteine deficiency induced browning and weight loss is dependent on sympathetic nervous system derived noradrenaline signaling via β3-adrenergic-receptors and does not require UCP1. Therapeutically, in high-fat diet fed obese mice, one week of cysteine-deficiency caused 30% weight-loss and reversed inflammation. These findings thus establish that cysteine is essential for organismal metabolism as removal of cysteine in the host triggers adipose browning and rapid weight loss.
热量限制(CR)和蛋氨酸限制等延长寿命的饮食干预措施会诱导白色脂肪组织(WAT)“褐变”,这是一种适应性代谢反应,可增加热量产生以维持健康。然而,饮食如何影响脂肪褐变和代谢健康尚不清楚。在这里,我们发现人类CR诱导的体重减轻会降低WAT中的半胱氨酸浓度,这表明这种氨基酸的消耗可能与CR的代谢益处有关。为了研究半胱氨酸对机体代谢的作用,我们创建了一种半胱氨酸缺乏小鼠模型,在该模型中,饮食中的半胱氨酸被去除,并且合成半胱氨酸的酶胱硫醚γ-裂解酶(CTH)被条件性敲除。使用这个动物模型,我们发现全身半胱氨酸耗竭会导致体重急剧下降,同时脂肪利用率增加和脂肪组织褐变。在半胱氨酸缺乏的小鼠中恢复饮食中的半胱氨酸可挽救体重减轻,同时以按需方式逆转脂肪褐变并增加食物摄入量。从机制上讲,半胱氨酸缺乏诱导的褐变和体重减轻依赖于交感神经系统衍生的去甲肾上腺素信号通过β3-肾上腺素能受体,并且不需要UCP1。在治疗方面,在高脂饮食喂养的肥胖小鼠中,一周的半胱氨酸缺乏导致体重减轻30%并逆转炎症。因此,这些发现表明半胱氨酸对机体代谢至关重要,因为宿主中半胱氨酸的去除会引发脂肪褐变和快速体重减轻。