Role of nuclear unphosphorylated STAT3 in angiotensin II type 1 receptor-induced cardiac hypertrophy

Cardiovasc Res. 2010 Jan 1;85(1):90-9. doi: 10.1093/cvr/cvp285.

Abstract

Aims: Cardiac hypertrophy is a risk factor independent of blood pressure; however, the mechanisms that distinguish pathological remodelling due to local cues from pressure overload are unresolved. This study was aimed at discovering a novel gene expression mechanism in heart failure.

Methods and results: In angiotensin II type 1 receptor (AT1R) transgenic mice (TG), we found a significant increase of mRNA and total STAT3 (T-STAT3) protein, but not STAT3 phosphorylated at residues Y705 and S727. A net increase in nuclear accumulation of this unphosphorylated form of STAT3 (U-STAT3) correlated with the development of cardiac hypertrophy and dysfunction, which are associated with abnormal expression of osteopontin and regulator of G protein signalling 2 genes. Nuclear accumulation of U-STAT3 is induced by angiotensin II treatment in neonatal cardiac myocytes, fibroblasts, and AT1R-expressing human embryonic kidney 293 (HEK-AT1R) cells. Chromatin immunoprecipitation demonstrated that U-STAT3 binds to the target gene promoter, and siRNA-mediated knockdown of STAT3 expression significantly altered the expression of target genes in HEK-AT1R cells. T-STAT3 in TG mouse hearts and the phosphorylation-deficient Y705F mutant STAT3 in HEK-AT1R cells physically interacted with transcription co-activator p300.

Conclusion: Chronic activation of AT1R induces unregulated expression of the Stat3 gene, leading to nuclear accumulation of U-STAT3, which significantly correlated with progression of cardiac hypertrophy.

Publication types

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

MeSH terms

  • Animals
  • Cardiomegaly / etiology*
  • Cardiomegaly / metabolism
  • Cell Nucleus / metabolism*
  • Cells, Cultured
  • Gene Expression Regulation
  • Mice
  • Mice, Inbred C57BL
  • Myocytes, Cardiac / metabolism*
  • Osteoprotegerin / physiology
  • Phosphorylation
  • RGS Proteins / physiology
  • Receptor, Angiotensin, Type 1 / physiology*
  • STAT3 Transcription Factor / genetics
  • STAT3 Transcription Factor / metabolism*
  • p300-CBP Transcription Factors / physiology

Substances

  • Osteoprotegerin
  • RGS Proteins
  • Receptor, Angiotensin, Type 1
  • Rgs2 protein, mouse
  • STAT3 Transcription Factor
  • Stat3 protein, mouse
  • p300-CBP Transcription Factors