Pathological changes of myocardial cytoskeleton in cardiomyopathic hamster

Mol Cell Biochem. 1995 Mar 9;144(1):75-9. doi: 10.1007/BF00926743.

Abstract

Immunocytochemical investigation was performed on the cytoskeletal proteins in cardiac tissue of the cardiomyopathic hamster. Male cardiomyopathic UM-X7.1 hamsters at 180 days of age (n = 8) and age- and sex-matched normal BIO-RB hamsters (n = 8) were used in this study. Immunofluorescence microscopy using monoclonal antibodies against desmin, alpha-actinin, titin, and vincullin was employed. The heart weight to body weight ratio was significantly increased in the heart of cardiomyopathic hamster compared with that of normal hamster. In cardiomyopathic hamster, the left ventricular cavity was markedly dilated. Light microscopically, hypertrophy and atrophy of myocytes and myocardial fibrosis were prominently observed in cardiomyopathic myocardium. Immunocytochemically, desmin, alpha-actinin and titin showed the cross striations along the myofibers in normal myocardium. In contrast, in cardiomyopathic myocardium, desmin was irregularly distributed in myocytes and the amount of desmin was increased. Loss of cross striations of alpha-actinin and titin were frequently observed. Immunofluorescence against vinculin was not significantly altered. We conclude that the alterations of cytoskeletal proteins in myocardial cells may relate to decreased myocardial function in cardiomyopathic hamster failing heart.

MeSH terms

  • Actinin / analysis
  • Animals
  • Body Weight
  • Cardiomyopathies / metabolism
  • Cardiomyopathies / pathology*
  • Cell Size
  • Collagen / analysis
  • Connectin
  • Cricetinae
  • Cytoskeletal Proteins / analysis*
  • Cytoskeleton / chemistry*
  • Cytoskeleton / ultrastructure
  • Desmin / analysis
  • Immunohistochemistry
  • Male
  • Muscle Proteins / analysis
  • Myocardium / chemistry
  • Myocardium / ultrastructure*
  • Organ Size
  • Protein Kinases*
  • Vinculin / analysis

Substances

  • Connectin
  • Cytoskeletal Proteins
  • Desmin
  • Muscle Proteins
  • Actinin
  • Vinculin
  • Collagen
  • Protein Kinases