AI Article Synopsis

  • AMP-activated protein kinase (AMPK) plays a critical role in regulating muscle stem cell (MuSC) self-renewal and differentiation, impacting tissue repair.
  • AMPKα1 MuSCs showed increased self-renewal but poor muscle regeneration due to a shift in their metabolism toward higher glycolysis, resembling a Warburg effect.
  • Lactate dehydrogenase (LDH) is a key regulator in this process, where its overexpression mimics the AMPKα1 effects, pushing MuSCs towards quiescence, while LDH inhibition promotes self-renewal, indicating metabolism's crucial role in stem cell fate.

Article Abstract

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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5494470PMC
http://dx.doi.org/10.15252/embj.201695273DOI Listing

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