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AMPKα1-LDH pathway regulates muscle stem cell self-renewal by controlling metabolic homeostasis.

Marine TheretLinda GsaierBethany SchafferGaëtan JubanSabrina Ben LarbiMichèle Weiss-GayetLaurent BultotCaterina CollodetMarc ForetzDominique DesplanchesPascual SanzZizhao ZangLin YangGuillaume VialBenoit ViolletKei SakamotoAnne BrunetBénédicte ChazaudRemi Mounier
Published in: The EMBO journal (2017)
Control of stem cell fate to either enter terminal differentiation versus returning to quiescence (self-renewal) is crucial for tissue repair. Here, we showed that AMP-activated protein kinase (AMPK), the master metabolic regulator of the cell, controls muscle stem cell (MuSC) self-renewal. AMPKα1-/- MuSCs displayed a high self-renewal rate, which impairs muscle regeneration. AMPKα1-/- MuSCs showed a Warburg-like switch of their metabolism to higher glycolysis. We identified lactate dehydrogenase (LDH) as a new functional target of AMPKα1. LDH, which is a non-limiting enzyme of glycolysis in differentiated cells, was tightly regulated in stem cells. In functional experiments, LDH overexpression phenocopied AMPKα1-/- phenotype, that is shifted MuSC metabolism toward glycolysis triggering their return to quiescence, while inhibition of LDH activity rescued AMPKα1-/- MuSC self-renewal. Finally, providing specific nutrients (galactose/glucose) to MuSCs directly controlled their fate through the AMPKα1/LDH pathway, emphasizing the importance of metabolism in stem cell fate.
Keyphrases
  • stem cells
  • protein kinase
  • skeletal muscle
  • cell fate
  • cell therapy
  • transcription factor
  • insulin resistance
  • metabolic syndrome
  • blood pressure
  • adipose tissue
  • signaling pathway