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TFEB 通过饥饿诱导的自调节环控制细胞脂质代谢。

TFEB controls cellular lipid metabolism through a starvation-induced autoregulatory loop.

机构信息

Telethon Institute of Genetics and Medicine (TIGEM), Naples, Italy.

出版信息

Nat Cell Biol. 2013 Jun;15(6):647-58. doi: 10.1038/ncb2718. Epub 2013 Apr 21.

Abstract

The lysosomal-autophagic pathway is activated by starvation and plays an important role in both cellular clearance and lipid catabolism. However, the transcriptional regulation of this pathway in response to metabolic cues is uncharacterized. Here we show that the transcription factor EB (TFEB), a master regulator of lysosomal biogenesis and autophagy, is induced by starvation through an autoregulatory feedback loop and exerts a global transcriptional control on lipid catabolism via Ppargc1α and Ppar1α. Thus, during starvation a transcriptional mechanism links the autophagic pathway to cellular energy metabolism. The conservation of this mechanism in Caenorhabditis elegans suggests a fundamental role for TFEB in the evolution of the adaptive response to food deprivation. Viral delivery of TFEB to the liver prevented weight gain and metabolic syndrome in both diet-induced and genetic mouse models of obesity, suggesting a new therapeutic strategy for disorders of lipid metabolism.

摘要

溶酶体自噬途径可被饥饿激活,在细胞清除和脂质分解代谢中发挥重要作用。然而,其对代谢信号的转录调控尚不清楚。本研究表明,转录因子 EB(TFEB)是溶酶体生物发生和自噬的主要调节因子,可通过自反馈回路被饥饿诱导,通过 Ppargc1α 和 Ppar1α 对脂质分解代谢发挥全局性转录控制作用。因此,在饥饿期间,一种转录机制将自噬途径与细胞能量代谢联系起来。该机制在秀丽隐杆线虫中的保守性表明 TFEB 在适应饥饿的进化过程中具有重要作用。TFEB 通过病毒递送至肝脏,可预防饮食诱导和肥胖遗传小鼠模型的体重增加和代谢综合征,提示这为脂质代谢紊乱提供了一种新的治疗策略。

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