Fasting-induced FGF21 signaling activates hepatic autophagy and lipid degradation via JMJD3 histone demethylase

Nat Commun. 2020 Feb 10;11(1):807. doi: 10.1038/s41467-020-14384-z.

Abstract

Autophagy is essential for cellular survival and energy homeostasis under nutrient deprivation. Despite the emerging importance of nuclear events in autophagy regulation, epigenetic control of autophagy gene transcription remains unclear. Here, we report fasting-induced Fibroblast Growth Factor-21 (FGF21) signaling activates hepatic autophagy and lipid degradation via Jumonji-D3 (JMJD3/KDM6B) histone demethylase. Upon FGF21 signaling, JMJD3 epigenetically upregulates global autophagy-network genes, including Tfeb, Atg7, Atgl, and Fgf21, through demethylation of histone H3K27-me3, resulting in autophagy-mediated lipid degradation. Mechanistically, phosphorylation of JMJD3 at Thr-1044 by FGF21 signal-activated PKA increases its nuclear localization and interaction with the nuclear receptor PPARα to transcriptionally activate autophagy. Administration of FGF21 in obese mice improves defective autophagy and hepatosteatosis in a JMJD3-dependent manner. Remarkably, in non-alcoholic fatty liver disease patients, hepatic expression of JMJD3, ATG7, LC3, and ULK1 is substantially decreased. These findings demonstrate that FGF21-JMJD3 signaling epigenetically links nutrient deprivation with hepatic autophagy and lipid degradation in mammals.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Autophagy / drug effects
  • Autophagy / genetics*
  • Epigenesis, Genetic
  • Fasting / metabolism*
  • Fatty Liver / metabolism
  • Fatty Liver / prevention & control
  • Fibroblast Growth Factors / administration & dosage
  • Fibroblast Growth Factors / deficiency
  • Fibroblast Growth Factors / metabolism*
  • Hepatocytes / metabolism
  • Humans
  • Jumonji Domain-Containing Histone Demethylases / genetics
  • Jumonji Domain-Containing Histone Demethylases / metabolism*
  • Klotho Proteins
  • Lipolysis
  • Liver / metabolism*
  • Male
  • Membrane Proteins / metabolism
  • Mice
  • Mice, Knockout
  • Mice, Obese
  • PPAR alpha / metabolism
  • Phosphorylation
  • Protein Binding
  • Signal Transduction
  • Up-Regulation

Substances

  • Klb protein, mouse
  • Membrane Proteins
  • PPAR alpha
  • Ppara protein, mouse
  • fibroblast growth factor 21
  • Fibroblast Growth Factors
  • Jumonji Domain-Containing Histone Demethylases
  • Kdm6b protein, mouse
  • Klotho Proteins