Cysteine depletion triggers adipose tissue thermogenesis and weight-loss

Aileen H. Lee, Lucie Orliaguet, Yun-Hee Youm, Rae Maeda, Tamara Dlugos, Yuanjiu Lei, Daniel Coman, Irina Shchukina, Sairam Andhey, Steven R. Smith, Eric Ravussin, Krisztian Stadler, Fahmeed Hyder, Maxim N. Artyomov, Yuki Sugiura, Vishwa Deep Dixit
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Abstract

Dietary interventions such as caloric restriction (CR)1 and methionine restriction2 that prolong lifespan induce the ‘browning’ of white adipose tissue (WAT), an adaptive metabolic response that increases heat production to maintain health3,4. However, how diet influences adipose browning and metabolic health is unclear. Here, we identified that weight-loss induced by CR in humans5 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)6, 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.
半胱氨酸耗竭引发脂肪组织产热和减肥
热量限制(CR)1 和蛋氨酸限制2 等能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3,4。然而,饮食如何影响脂肪褐变和代谢健康尚不清楚。在这里,我们发现人类通过减肥诱导的 CR5 会降低 WAT 中半胱氨酸的浓度,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,我们创建了半胱氨酸缺乏小鼠模型,在该模型中,膳食中的半胱氨酸被消除,合成半胱氨酸的酶--胱硫醚γ-裂解酶(CTH)6 被有条件地删除。利用这种动物模型,我们发现全身性半胱氨酸缺乏会导致体重急剧下降,同时脂肪利用率增加,脂肪组织变褐。在半胱氨酸缺乏的小鼠中恢复膳食半胱氨酸可挽救体重下降,同时逆转脂肪褐变和按需增加食物摄入。从机理上讲,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通过β3-肾上腺素能受体产生的去甲肾上腺素信号,而不需要UCP1。从治疗角度看,在高脂饮食喂养的肥胖小鼠中,一周的半胱氨酸缺乏会导致体重下降 30%,并逆转炎症。因此,这些研究结果表明,半胱氨酸对生物体的新陈代谢至关重要,因为在宿主体内去除半胱氨酸会引发脂肪褐变和体重迅速下降。
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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