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Ectopic fat deposition contributes to age-associated pathology in Caenorhabditis elegans

机译:异位脂肪沉积导致秀丽隐杆线虫的年龄相关病理

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摘要

Age-dependent collapse of lipid homeostasis results in spillover of lipids and excessive fat deposition in nonadipose tissues. Ectopic fat contributes to lipotoxicity and has been implicated in the development of a metabolic syndrome that increases risk of age-associated diseases. However, the molecular mechanisms coupling ectopic fat accumulation with aging remain obscure. Here, we use nonlinear imaging modalities to visualize and quantify age-dependent ectopic lipid accumulation in Caenorhabditis elegans. We find that aging is accompanied by pronounced deposition of lipids in nonadipose tissues, including the nervous system. Importantly, interventions that promote longevity such as low insulin signaling, germ-line loss, and dietary restriction, which effectively delay aging in evolutionary divergent organisms, diminish the rate of ectopic fat accumulation and the size of lipid droplets. Suppression of lipotoxic accumulation of fat in heterologous tissues is dependent on helix-loop-helix (HLH)-30/transcription factor EB (TFEB) and autophagy. Our findings in their totality highlight the pivotal role of HLH-30/TFEB and autophagic processes in the maintenance of lipid homeostasis during aging, in addition to establishing nonlinear imaging as a powerful tool for monitoring ectopic lipid droplet deposition in vivo.
机译:脂质稳态的年龄依赖性崩溃会导致脂质溢出和非脂肪组织中过多的脂肪沉积。异位脂肪有助于脂毒性,并且与代谢综合征的发展有关,代谢综合征增加了与年龄有关的疾病的风险。但是,结合异位脂肪积累与衰老的分子机制仍然不清楚。在这里,我们使用非线性成像方式来可视化和量化秀丽隐杆线虫的年龄依赖性异位脂质堆积。我们发现衰老伴随着脂质在非脂肪组织(包括神经系统)中的沉积。重要的是,可延长寿命的干预措施,例如低胰岛素信号传导,种系丧失和饮食限制,可有效延迟进化趋异生物体内的衰老,从而减少异位脂肪堆积的速度和脂质滴的大小。异源组织中脂肪脂毒性积累的抑制取决于螺旋-环-螺旋(HLH)-30 /转录因子EB(TFEB)和自噬。我们的发现总体上突出了HLH-30 / TFEB和自噬过程在衰老过程中维持脂质稳态的关键作用,此外还建立了非线性成像作为监测体内异位脂质液滴沉积的有力工具。

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