Suppression of proliferation and cardiomyocyte hypertrophy by CHAMP, a cardiac-specific RNA helicase

  1. Zhi-Ping Liu and
  2. Eric N. Olson*
  1. Department of Molecular Biology, University of Texas Southwestern Medical Center, 6000 Harry Hines Boulevard, Dallas, TX 75239-9041
  1. Contributed by Eric N. Olson

Abstract

Adult cardiomyocytes are irreversibly postmitotic but respond to a variety of stimuli by hypertrophic growth, which is associated with an increase in cell size and protein content, organization of sarcomeres, and activation of a fetal gene program. Recently, we described a novel cardiac helicase activated by MEF2 protein (CHAMP), which is expressed specifically in the heart throughout prenatal and postnatal development. Here we show that CHAMP acts as an inhibitor of cell proliferation and cardiomyocyte hypertrophy. Ectopic expression of CHAMP inhibits proliferation of HeLa cells and blocks cell cycle entry of serum-stimulated NIH 3T3 cells. Overexpression of CHAMP in primary neonatal cardiomyocytes blocks hypertrophic growth and the induction of fetal genes in response to stimulation by serum and phenylephrine but does not prevent sarcomere organization or early mitogenic signaling events including activation of extracellular signal-regulated kinases or up-regulation of c-fos. Inhibition of cardiomyocyte hypertrophy by CHAMP requires the conserved ATPase domain and is accompanied by up-regulation of the cyclin-dependent protein kinase inhibitor p21CIP1. These findings identify CHAMP as a cardiac-specific suppressor of cardiomyocyte hypertrophy and cell cycle progression and suggest that CHAMP may suppress these processes through the regulation of p21CIP1.

Footnotes

  • * To whom reprint requests should be addressed. E-mail: eolson{at}hamon.swmed.edu.

  • Abbreviations:
    ANF,
    atrial natriuretic factor;
    CDK,
    cyclin-dependent kinase;
    CDKI,
    cyclin-dependent kinase inhibitor;
    CHAMP,
    cardiac helicase activated by MEF2 protein;
    adCHAMP,
    adenovirus encoding FLAG-tagged CHAMP;
    E,
    embryonic day;
    ERK,
    extracellular signal-regulated kinase;
    MAPK,
    mitogen-activated protein kinase;
    MHC,
    myosin heavy chain;
    MOI,
    multiplicity of infection;
    PCNA,
    proliferating cellular nuclear antigen;
    PE,
    phenylephrine;
    adβ-gal,
    adenovirus that constitutively expresses β-galactosidase
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