4.8 Article

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

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NATURE CELL BIOLOGY
卷 15, 期 6, 页码 647-+

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NATURE PUBLISHING GROUP
DOI: 10.1038/ncb2718

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资金

  1. Italian Telethon Foundation [TGM11CB6, TGM11SB1]
  2. Beyond Batten Disease Foundation
  3. European Research Council [250154]
  4. March of Dimes [6-FY11-306]
  5. US National Institutes of Health [R01-NS078072, R01-HL51586]
  6. Diabetes and Endocrinology Research Center [P30-DK079638]
  7. Mouse Metabolism Core at Baylor College of Medicine
  8. Cancer Prevention and Research Institute of Texas [RP110390]
  9. Fund for Medical Discovery postdoctoral fellowship from the Massachusetts General Hospital
  10. National Institute of General Medical Sciences of the National Institutes of Health [R01GM101056-01]

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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 Ppargc 1 alpha and Ppar 1 alpha. 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.

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