NRG-1-induced cardiomyocyte hypertrophy. Role of PI-3-kinase, p70(S6K), and MEK-MAPK-RSK

Ragavendra R. Baliga, David R. Pimental, You Yang Zhao, William W. Simmons, Mark A. Marchionni, Douglas B. Sawyer, Ralph A. Kelly*

*Corresponding author for this work

Research output: Contribution to journalArticle

135 Scopus citations

Abstract

Neuregulins are a family of growth-promoting peptides known to be important in neural and mesenchymal tissue development. Targeted disruption of neuregulin (NRG)-1 or one of two of its cognate receptors, ErbB2 or ErbB4, results in embryonic lethality because of failure of the heart to develop. Although expression of NRGs and their receptors declines after midembryogenesis, both ErbB2 and ErbB4 are present in cardiac myocytes, and NRG-1 expression remains inducible in primary cultures of coronary microvascular endothelial cells from adult rat ventricular muscle. In neonatal rat ventricular myocytes, a soluble NRG-1, recombinant human glial growth factor-2, increased [3H]phenylalanine uptake and induced expression of atrial natriuretic factor (ANF) and sarcomeric F-actin polymerization. The effect of NRG-1 on [3H]phenylalanine uptake and sarcomeric F-actin polymerization was maximal at 20 ng/ml but declined at higher concentrations. NRG-1 activated p42/p44 mitogen-activated protein kinase (MAPK) [extracellular signal-regulated kinase (ERK)-2/ERK1] and ribosomal S6 kinase (RSK)-2 (90-kDa ribosomal S6 kinase), both of which could be inhibited by the MAPK/ERK kinase-1 antagonist PD-098059. NRG-1 also activated 70-kDa ribosomal S6 kinase, which was inhibited by either rapamycin or wortmannin. Activation of these pathways exhibited the same 'biphasic' response to increasing NRG-1 concentrations. Wortmannin and LY-294002 blocked sarcomeric F-actin polymerization but not [3H]phenylalanine uptake or ANF expression, whereas PD-098059 consistently blocked both [3H]phenylalanine uptake and ANF expression but not actin polymerization. In contrast, rapamycin inhibited [3H]phenylalanine uptake and F-actin polymerization but not ANF expression. Thus NRG-ErbB signaling triggers multiple nonredundant pathways in postnatal ventricular myocytes.

Original languageEnglish (US)
Pages (from-to)H2026-H2037
JournalAmerican Journal of Physiology - Heart and Circulatory Physiology
Volume277
Issue number5 46-5
DOIs
StatePublished - Nov 1999

Keywords

  • 70- kDa ribosomal S6 kinase
  • Cardiac myocyte
  • ErbB receptors
  • Extracellular signal-regulated kinase
  • Glial growth factor
  • Mitogen-activated protein kinase
  • Mitogen-activated protein kinase/extracellular signal-regulated kinase kinase
  • Neuregulin-1
  • PD-098059
  • Phosphoinositide 3-kinase
  • Ribosomal S6 kinase
  • Wortmannin

ASJC Scopus subject areas

  • Physiology
  • Cardiology and Cardiovascular Medicine
  • Physiology (medical)

Fingerprint Dive into the research topics of 'NRG-1-induced cardiomyocyte hypertrophy. Role of PI-3-kinase, p70(S6K), and MEK-MAPK-RSK'. Together they form a unique fingerprint.

Cite this