Activated glycogen synthase-3 beta suppresses cardiac hypertrophy in vivo

Proc Natl Acad Sci U S A. 2002 Jan 22;99(2):907-12. doi: 10.1073/pnas.231619298. Epub 2002 Jan 8.

Abstract

The adult myocardium responds to a variety of pathologic stimuli by hypertrophic growth that frequently progresses to heart failure. The calcium/calmodulin-dependent protein phosphatase calcineurin is a potent transducer of hypertrophic stimuli. Calcineurin dephosphorylates members of the nuclear factor of activated T cell (NFAT) family of transcription factors, which results in their translocation to the nucleus and activation of calcium-dependent genes. Glycogen synthase kinase-3 (GSK-3) phosphorylates NFAT proteins and antagonizes the actions of calcineurin by stimulating NFAT nuclear export. To determine whether activated GSK-3 can act as an antagonist of hypertrophic signaling in the adult heart in vivo, we generated transgenic mice that express a constitutively active form of GSK-3 beta under control of a cardiac-specific promoter. These mice were physiologically normal under nonstressed conditions, but their ability to mount a hypertrophic response to calcineurin activation was severely impaired. Similarly, cardiac-specific expression of activated GSK-3 beta diminished hypertrophy in response to chronic beta-adrenergic stimulation and pressure overload. These findings reveal a role for GSK-3 beta as an inhibitor of hypertrophic signaling in the intact myocardium and suggest that elevation of cardiac GSK-3 beta activity may provide clinical benefit in the treatment of pathologic hypertrophy and heart failure.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Calcineurin / metabolism
  • Calcium-Calmodulin-Dependent Protein Kinases / genetics*
  • Calcium-Calmodulin-Dependent Protein Kinases / metabolism*
  • Cardiomegaly / etiology
  • Cardiomegaly / metabolism
  • Cardiomegaly / prevention & control*
  • DNA-Binding Proteins / metabolism
  • Enzyme Activation
  • Gene Expression
  • Glycogen Synthase Kinase 3
  • Glycogen Synthase Kinases
  • Isoproterenol / pharmacology
  • Mice
  • Mice, Transgenic
  • Models, Biological
  • Myosin Heavy Chains / genetics
  • NFATC Transcription Factors
  • Nuclear Proteins*
  • Signal Transduction
  • Transcription Factors / metabolism

Substances

  • DNA-Binding Proteins
  • NFATC Transcription Factors
  • Nuclear Proteins
  • Transcription Factors
  • Glycogen Synthase Kinases
  • Calcium-Calmodulin-Dependent Protein Kinases
  • Glycogen Synthase Kinase 3
  • Calcineurin
  • Myosin Heavy Chains
  • Isoproterenol