Testosterone inhibits transforming growth factor-β signaling during myogenic differentiation and proliferation of mouse satellite cells: potential role of follistatin in mediating testosterone action

Mol Cell Endocrinol. 2012 Mar 5;350(1):39-52. doi: 10.1016/j.mce.2011.11.019. Epub 2011 Nov 25.

Abstract

Testosterone (T) administration is associated with increased satellite cell number and skeletal muscle hypertrophy, although there is considerable heterogeneity in the response of different skeletal muscle groups to T in vivo. We investigated the effects of T on the growth and differentiation of satellite cells isolated from levator ani (LA) and gastrocnemius (gastroc) muscles. T up regulated follistatin (Fst) expression, but down regulated the mRNA and protein expression of a number of genes in the transforming growth factor-beta (TGF-β)-signaling pathway. Inhibition of Fst expression by small interfering RNA (siRNA) inhibited myogenic differentiation and blocked the pro-myogenic effects of T. Treatment of satellite cells with T or Fst up regulated the expression of Pax7 and PCNA, and increased their proliferation. T and Fst blocked TGF-β induced inhibition of growth and myogenic differentiation and down regulated TGF-β-dependent transcriptome in both LA and gastroc cells. We conclude that T stimulation of satellite cell proliferation and myogenic differentiation are associated with up regulation of Fst and inhibition of TGF-β-signaling.

Publication types

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

MeSH terms

  • Animals
  • Bone Morphogenetic Proteins / physiology
  • Cell Differentiation*
  • Cell Proliferation*
  • Cells, Cultured
  • Follistatin / genetics
  • Follistatin / metabolism
  • Follistatin / physiology*
  • Gene Expression
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Muscle Development*
  • Muscle, Skeletal / cytology
  • Muscle, Skeletal / physiology
  • Myosin Heavy Chains / genetics
  • Myosin Heavy Chains / metabolism
  • PAX7 Transcription Factor / genetics
  • PAX7 Transcription Factor / metabolism
  • Phosphorylation
  • Primary Cell Culture
  • Receptors, Androgen / metabolism
  • Satellite Cells, Skeletal Muscle / metabolism
  • Satellite Cells, Skeletal Muscle / physiology*
  • Signal Transduction
  • Smad Proteins / metabolism
  • Testosterone / pharmacology
  • Testosterone / physiology*
  • Transforming Growth Factor beta / pharmacology
  • Transforming Growth Factor beta / physiology*
  • Up-Regulation

Substances

  • Bone Morphogenetic Proteins
  • Follistatin
  • PAX7 Transcription Factor
  • Pax7 protein, mouse
  • Receptors, Androgen
  • Smad Proteins
  • Transforming Growth Factor beta
  • Testosterone
  • Myosin Heavy Chains