Peroxisome proliferator-activated receptor beta activation promotes myonuclear accretion in skeletal muscle of adult and aged mice

Pflugers Arch. 2009 Sep;458(5):901-13. doi: 10.1007/s00424-009-0676-9. Epub 2009 May 5.

Abstract

We reported recently that peroxisome proliferator-activated receptor beta (PPARbeta) activation promotes a calcineurin-dependent exercise-like remodelling characterised by increased numbers of oxidative fibres and capillaries. As physical exercise also induces myonuclear accretion, we investigated whether PPARbeta activation alters myonuclear density. Transgenic muscle-specific PPARbeta over-expression induced 14% increase of myonuclear density. Pharmacological PPARbeta activation promoted rapid and massive myonuclear accretion (20% increase after 48 h), which is dependent upon calcineurin/nuclear factor of activated T cells signalling pathway. In vivo bromodeoxyuridine labelling and proliferating cell nuclear antigen immunodetection revealed that PPARbeta activation did not promote cell proliferation, suggesting that the PPARbeta-promoted myonuclear accretion involves fusion of pre-existing muscle precursor cells to myofibres rather than cell division. Finally, we showed that in skeletal muscle, ageing led to a down-regulation of PPARbeta accompanied by decrease of both oxidative fibre number and myonuclear density. PPARbeta pharmacological activation counteracts, at least in part, the ageing-driven muscle remodelling.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aging / drug effects
  • Aging / pathology
  • Aging / physiology*
  • Animals
  • Calcineurin / metabolism
  • Calcineurin Inhibitors
  • Cell Division / drug effects
  • Cell Fusion
  • Cell Nucleus / physiology*
  • Citrate (si)-Synthase / metabolism
  • Cyclosporine / pharmacology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred Strains
  • Mice, Transgenic
  • Muscle Fibers, Fast-Twitch / cytology
  • Muscle Fibers, Fast-Twitch / metabolism
  • Muscle Fibers, Fast-Twitch / pathology
  • Muscle Fibers, Skeletal / cytology
  • Muscle Fibers, Skeletal / metabolism
  • Muscle Fibers, Skeletal / pathology
  • Muscle, Skeletal / cytology*
  • Muscle, Skeletal / drug effects
  • Muscle, Skeletal / metabolism
  • Muscle, Skeletal / pathology
  • NFATC Transcription Factors / metabolism
  • PPAR-beta / agonists
  • PPAR-beta / physiology*
  • Proliferating Cell Nuclear Antigen / metabolism
  • Satellite Cells, Skeletal Muscle / cytology
  • Satellite Cells, Skeletal Muscle / drug effects
  • Succinate Dehydrogenase / metabolism
  • Thiazoles / pharmacology

Substances

  • Calcineurin Inhibitors
  • NFATC Transcription Factors
  • Nfatc1 protein, mouse
  • Nfatc3 protein, mouse
  • PPAR-beta
  • Proliferating Cell Nuclear Antigen
  • Thiazoles
  • (4-(((2-(3-fluoro-4-(trifluoromethyl)phenyl)-4-methyl-1,3-thiazol-5-yl)methyl)sulfanyl)-2-methylphenoxy)acetic acid
  • Cyclosporine
  • Succinate Dehydrogenase
  • Citrate (si)-Synthase
  • Calcineurin