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High-fat diet triggers inflammation-induced cleavage of SIRT1 in adipose tissue to promote metabolic dysfunction

机译:高脂饮食触发脂肪组织中SIRT1的炎症诱导裂解,从而促进代谢功能障碍

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摘要

Adipose tissue plays an important role in storing excess nutrients and preventing ectopic lipid accumulation in other organs. Obesity leads to excess lipid storage in adipocytes, resulting in the generation of stress signals and the derangement of metabolic functions. SIRT1 is an important regulatory sensor of nutrient availability in many metabolic tissues. Here we report that SIRT1 functions in adipose tissue to protect from inflammation and obesity under normal feeding conditions, and to forestall the progression to metabolic dysfunction under dietary stress and aging. Genetic ablation of SIRT1 in adipose tissue leads to gene expression changes that highly overlap with changes induced by high-fat diet in wild-type mice, suggesting that dietary stress signals inhibit the activity of SIRT1. Indeed, we show that high-fat diet induces the cleavage of SIRT1 protein in adipose tissue by the inflammation-activated caspase-1, providing a link between dietary stress and predisposition to metabolic dysfunction. ? 2012 Elsevier Inc.
机译:脂肪组织在储存过量营养物和防止异位脂质在其他器官中积聚方面起着重要作用。肥胖会导致脂肪细胞中过多的脂质储存,从而导致应激信号的产生和代谢功能的紊乱。 SIRT1是许多代谢组织中养分利用率的重要调控传感器。在这里,我们报道SIRT1在脂肪组织中起作用,以保护其在正常喂养条件下免于发炎和肥胖,并防止在饮食压力和衰老下进展为代谢功能障碍。脂肪组织中SIRT1的遗传消融导致基因表达变化与高脂饮食在野生型小鼠中诱导的变化高度重叠,这表明饮食压力信号抑制了SIRT1的活性。确实,我们表明高脂饮食通过炎症激活的caspase-1诱导脂肪组织中SIRT1蛋白的裂解,从而在饮食压力和易患代谢功能障碍之间提供了联系。 ? 2012爱思唯尔公司

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