Insulin-like growth factor-1 (IGF-1) inversely regulates atrophy-induced genes via the phosphatidylinositol 3-kinase/Akt/mammalian target of rapamycin (PI3K/Akt/mTOR) pathway

J Biol Chem. 2005 Jan 28;280(4):2737-44. doi: 10.1074/jbc.M407517200. Epub 2004 Nov 17.

Abstract

Skeletal muscle size is regulated by anabolic (hypertrophic) and catabolic (atrophic) processes. We first characterized molecular markers of both hypertrophy and atrophy and identified a small subset of genes that are inversely regulated in these two settings (e.g. up-regulated by an inducer of hypertrophy, insulin-like growth factor-1 (IGF-1), and down-regulated by a mediator of atrophy, dexamethasone). The genes identified as being inversely regulated by atrophy, as opposed to hypertrophy, include the E3 ubiquitin ligase MAFbx (also known as atrogin-1). We next sought to investigate the mechanism by which IGF-1 inversely regulates these markers, and found that the phosphatidylinositol 3-kinase/Akt/mammalian target of rapamycin (PI3K/Akt/mTOR) pathway, which we had previously characterized as being critical for hypertrophy, is also required to be active in order for IGF-1-mediated transcriptional changes to occur. We had recently demonstrated that the IGF1/PI3K/Akt pathway can block dexamethasone-induced up-regulation of the atrophy-induced ubiquitin ligases MuRF1 and MAFbx by blocking nuclear translocation of a FOXO transcription factor. In the current study we demonstrate that an additional step of IGF1 transcriptional regulation occurs downstream of mTOR, which is independent of FOXO. Thus both the Akt/FOXO and the Akt/mTOR pathways are required for the transcriptional changes induced by IGF-1.

MeSH terms

  • Active Transport, Cell Nucleus
  • Animals
  • Atrophy
  • Cell Differentiation
  • Cell Line
  • Cell Nucleus / metabolism
  • Dexamethasone / pharmacology
  • Dose-Response Relationship, Drug
  • Down-Regulation
  • Gene Expression Regulation
  • Gene Expression Regulation, Enzymologic*
  • Glucocorticoids / metabolism
  • Immunoblotting
  • Insulin-Like Growth Factor I / genetics
  • Insulin-Like Growth Factor I / physiology*
  • Mice
  • Muscle Proteins / metabolism
  • Oligonucleotide Array Sequence Analysis
  • Phenotype
  • Phosphatidylinositol 3-Kinases / metabolism*
  • Protein Kinases / metabolism*
  • Protein Serine-Threonine Kinases / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • SKP Cullin F-Box Protein Ligases / metabolism
  • Signal Transduction
  • TOR Serine-Threonine Kinases
  • Time Factors
  • Transcription, Genetic
  • Ubiquitin-Protein Ligases / metabolism

Substances

  • Glucocorticoids
  • Muscle Proteins
  • Insulin-Like Growth Factor I
  • Dexamethasone
  • FBXO32 protein, human
  • SKP Cullin F-Box Protein Ligases
  • Ubiquitin-Protein Ligases
  • Protein Kinases
  • MTOR protein, human
  • mTOR protein, mouse
  • Protein Serine-Threonine Kinases
  • TOR Serine-Threonine Kinases