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Skeletal muscle p53-depletion uncovers a mechanism of fuel usage suppression that enables efficient energy conservation.

Georgia Lenihan-GeelsFrancisco Garcia CarrizoMarina LeerSabrina GohlkeMoritz OsterSophie Pöhle-KronawitterChristiane OttAlexandra ChadtIsabel N ReinischMarkus GalhuberChen LiWenke JonasMarkus JähnertSusanne KlausHadi Al-HasaniTilman GruneAnnette SchürmannTobias MadlAndreas ProkeschMichael SchuppTim Julius Schulz
Published in: Journal of cachexia, sarcopenia and muscle (2024)
These findings suggest that efficient nutrient conservation is a key element of normal metabolic homeostasis that is sustained by p53. The homeostatic state in metabolic tissues is actively maintained to coordinate efficient energy conservation and metabolic flexibility towards nutrient stress. The acute deletion of Trp53 unlocks mechanisms that suppress the activity of nutrient catabolic pathways, causing substantial loss of intramuscular energy stores, which contributes to a fasting-like state in muscle tissue. Altogether, these findings uncover a novel function of p53 in the short-term regulation of nutrient metabolism in skeletal muscle and show that p53 serves to maintain metabolic homeostasis and efficient energy conservation.
Keyphrases
  • skeletal muscle
  • insulin resistance
  • gene expression
  • liver failure
  • type diabetes
  • blood pressure
  • intensive care unit
  • respiratory failure
  • stress induced