Gαi2 signaling promotes skeletal muscle hypertrophy, myoblast differentiation, and muscle regeneration

Sci Signal. 2011 Nov 29;4(201):ra80. doi: 10.1126/scisignal.2002038.

Abstract

Skeletal muscle atrophy results in loss of strength and an increased risk of mortality. We found that lysophosphatidic acid, which activates a G protein (heterotrimeric guanine nucleotide-binding protein)-coupled receptor, stimulated skeletal muscle hypertrophy through activation of Gα(i2). Expression of a constitutively active mutant of Gα(i2) stimulated myotube growth and differentiation, effects that required the transcription factor NFAT (nuclear factor of activated T cells) and protein kinase C. In addition, expression of the constitutively active Gα(i2) mutant inhibited atrophy caused by the cachectic cytokine TNFα (tumor necrosis factor-α) by blocking an increase in the abundance of the mRNA encoding the E3 ubiquitin ligase MuRF1 (muscle ring finger 1). Gα(i2) activation also enhanced muscle regeneration and caused a switch to oxidative fibers. Our study thus identifies a pathway that promotes skeletal muscle hypertrophy and differentiation and demonstrates that Gα(i2)-induced signaling can act as a counterbalance to MuRF1-mediated atrophy, indicating that receptors that act through Gα(i2) might represent potential targets for preventing skeletal muscle wasting.

MeSH terms

  • Animals
  • Cell Differentiation*
  • Enzyme Activation / genetics
  • GTP-Binding Protein alpha Subunits, G12-G13 / genetics
  • GTP-Binding Protein alpha Subunits, G12-G13 / metabolism*
  • HEK293 Cells
  • Humans
  • Hypertrophy / enzymology
  • Hypertrophy / genetics
  • Hypertrophy / pathology
  • Mice
  • Mice, Transgenic
  • Muscle Proteins / genetics
  • Muscle Proteins / metabolism
  • Muscular Atrophy / enzymology
  • Muscular Atrophy / genetics
  • Muscular Atrophy / pathology
  • Mutation
  • Myoblasts, Skeletal / enzymology*
  • Myoblasts, Skeletal / pathology
  • NFATC Transcription Factors / genetics
  • NFATC Transcription Factors / metabolism
  • Protein Kinase C / genetics
  • Protein Kinase C / metabolism
  • Regeneration*
  • Signal Transduction*
  • Tripartite Motif Proteins
  • Tumor Necrosis Factor-alpha / genetics
  • Tumor Necrosis Factor-alpha / metabolism
  • Ubiquitin-Protein Ligases / genetics
  • Ubiquitin-Protein Ligases / metabolism

Substances

  • Muscle Proteins
  • NFATC Transcription Factors
  • Tripartite Motif Proteins
  • Tumor Necrosis Factor-alpha
  • TRIM63 protein, human
  • Trim63 protein, mouse
  • Ubiquitin-Protein Ligases
  • Protein Kinase C
  • GTP-Binding Protein alpha Subunits, G12-G13