Literature DB >> 7802678

Ras activity is required for phenylephrine-induced activation of mitogen-activated protein kinase in cardiac muscle cells.

A Thorburn1.   

Abstract

The mitogen-activated protein (MAP) kinases are a family of kinases whose activity is implicated in a number of growth and differentiation responses. Recently, we and others have shown that these kinases are activated by agonists which induce cardiac muscle cell hypertrophy. Inhibition of MAP kinase activation prevents some of the phenotypes associated with phenylephrine-induced cardiac cell hypertrophy, indicating that this activation is of functional significance. In this communication, we show that active Ras can induce MAP kinase activation in cardiac muscle cells. In addition, phenylephrine-induced activation of the MAP kinases requires Ras activity since a dominant negative Ras mutant (Ala15Ras) and a Ras-blocking, Raf mutant (C4B Raf) prevent activation of the MAP kinase Erk2 by phenylephrine. These data indicate that phenylephrine signaling to the MAP kinases is mediated through Ras.

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Year:  1994        PMID: 7802678     DOI: 10.1006/bbrc.1994.2823

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  13 in total

Review 1.  Mitogen-activated protein kinase (MAPK) in cardiac tissues.

Authors:  C Page; A F Doubell
Journal:  Mol Cell Biochem       Date:  1996 Apr 12-26       Impact factor: 3.396

2.  A requirement for the rac1 GTPase in the signal transduction pathway leading to cardiac myocyte hypertrophy.

Authors:  J B Pracyk; K Tanaka; D D Hegland; K S Kim; R Sethi; I I Rovira; D R Blazina; L Lee; J T Bruder; I Kovesdi; P J Goldshmidt-Clermont; K Irani; T Finkel
Journal:  J Clin Invest       Date:  1998-09-01       Impact factor: 14.808

3.  AFos dissociates cardiac myocyte hypertrophy and expression of the pathological gene program.

Authors:  Mark Y Jeong; Koichiro Kinugawa; Charles Vinson; Carlin S Long
Journal:  Circulation       Date:  2005-03-28       Impact factor: 29.690

4.  MAP kinase- and Rho-dependent signals interact to regulate gene expression but not actin morphology in cardiac muscle cells.

Authors:  J Thorburn; S Xu; A Thorburn
Journal:  EMBO J       Date:  1997-04-15       Impact factor: 11.598

5.  Thyroid hormone drives fetal cardiomyocyte maturation.

Authors:  Natasha N Chattergoon; George D Giraud; Samantha Louey; Philip Stork; Abigail L Fowden; Kent L Thornburg
Journal:  FASEB J       Date:  2011-10-05       Impact factor: 5.191

6.  Cardiac-specific overexpression of RhoA results in sinus and atrioventricular nodal dysfunction and contractile failure.

Authors:  V P Sah; S Minamisawa; S P Tam; T H Wu; G W Dorn; J Ross; K R Chien; J H Brown
Journal:  J Clin Invest       Date:  1999-06       Impact factor: 14.808

7.  Inhibition of a signaling pathway in cardiac muscle cells by active mitogen-activated protein kinase kinase.

Authors:  J Thorburn; M Carlson; S J Mansour; K R Chien; N G Ahn; A Thorburn
Journal:  Mol Biol Cell       Date:  1995-11       Impact factor: 4.138

8.  Stimulation of gene expression in neonatal rat ventricular myocytes by Ras is mediated by Ral guanine nucleotide dissociation stimulator (Ral.GDS) and phosphatidylinositol 3-kinase in addition to Raf.

Authors:  S J Fuller; S G Finn; J Downward; P H Sugden
Journal:  Biochem J       Date:  1998-10-15       Impact factor: 3.857

9.  Acute hypertension activates mitogen-activated protein kinases in arterial wall.

Authors:  Q Xu; Y Liu; M Gorospe; R Udelsman; N J Holbrook
Journal:  J Clin Invest       Date:  1996-01-15       Impact factor: 14.808

10.  A Ras-dependent pathway regulates RNA polymerase II phosphorylation in cardiac myocytes: implications for cardiac hypertrophy.

Authors:  M Abdellatif; S E Packer; L H Michael; D Zhang; M J Charng; M D Schneider
Journal:  Mol Cell Biol       Date:  1998-11       Impact factor: 4.272

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