The gp130/STAT3 signaling pathway mediates beta-adrenergic receptor-induced atrial natriuretic factor expression in cardiomyocytes

FEBS J. 2008 Jul;275(14):3590-7. doi: 10.1111/j.1742-4658.2008.06504.x.

Abstract

beta-Adrenergic receptor (beta-AR)-induced cardiac remodeling is closely linked with the re-expression of the atrial natriuretic factor (ANF) gene. However, the exact molecular mechanism of this response remains elusive. Here, we demonstrate that the beta-AR agonist isoproterenol potently evokes the tyrosine phosphorylation of STAT3 and increases its transcriptional activity in an extracellularly regulated kinase 1/2 and glycoprotein (gp)130 signaling-dependent manner in rat cardiomyocytes. Interestingly, both specific silencing of signal transducers and activators of transcription 3 (STAT3) expression by lentivirus-mediated RNA interference and antagonism of gp130 signaling lead to significant inhibition of isoproterenol-stimulated ANF expression. Together, these results indicate that gp130/STAT3 signaling has an essential role in ANF expression by beta-AR stimulation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenergic beta-Agonists / pharmacology
  • Animals
  • Atrial Natriuretic Factor / biosynthesis*
  • Atrial Natriuretic Factor / genetics
  • Cells, Cultured
  • Cytokine Receptor gp130 / metabolism*
  • Cytokines / physiology
  • Extracellular Signal-Regulated MAP Kinases / physiology
  • Gene Expression
  • Isoproterenol / pharmacology
  • Myocytes, Cardiac / drug effects
  • Myocytes, Cardiac / metabolism*
  • Phosphorylation
  • Rats
  • Receptors, Adrenergic, beta / metabolism*
  • STAT3 Transcription Factor / chemistry
  • STAT3 Transcription Factor / metabolism*
  • Signal Transduction
  • Transcription, Genetic
  • Tyrosine / metabolism

Substances

  • Adrenergic beta-Agonists
  • Cytokines
  • Receptors, Adrenergic, beta
  • STAT3 Transcription Factor
  • Cytokine Receptor gp130
  • Tyrosine
  • Atrial Natriuretic Factor
  • Extracellular Signal-Regulated MAP Kinases
  • Isoproterenol