Comparative study of the roles of cytokines and apoptosis in dilated and hypertrophic cardiomyopathies

Eur Cytokine Netw. 2004 Jan-Mar;15(1):53-9.

Abstract

Aims: In order to gain more insight into the pathogenesis of dilated and hypertrophic cardiomyopathies (DCM and HCM, respectively), we investigated the roles of certain cytokines that regulate apoptosis.

Methods and results: ELISA tests, performed to determine the plasma concentrations of tumour necrosis factor-alpha (TNF-alpha), the soluble Fas (sFas), interleukin-6 (IL-6) and the soluble IL-6 receptor (sIL-6R), revealed that DCM patients exhibit elevated concentrations of TNF-alpha, sFas, IL-6 and sIL-6R, while HCM patients have only high IL-6 and sIL-6R levels as compared with healthy individuals. Western blot analysis of the levels of TNF-alpha, IL-6, Bcl-2 and Bax proteins in myocardium samples demonstrated that DCM patients express increased levels of TNF-alpha, IL-6 and Bax, whereas HCM heart lysates display only elevated levels of Bcl-2. Annexin V binding assay of TNF-alpha-treated H9C2 cells indicated that the in vitro cytotoxicity of this cytokine involves apoptotosis and necrosis.

Conclusion: In accord with previous observations, our data indicate a strong activation of the pro-apoptotic TNF and Fas pathways in DCM patients, and an anti-apoptotic shift in HCM patients. These findings have a bearing on the pathogenesis of cardiomyopathies, since apoptosis may account for certain dysfunctions observed in DCM, while IL-6 may elicit the hypertrophy characteristic of HCM.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Annexin A5 / analysis
  • Annexin A5 / biosynthesis
  • Apoptosis*
  • Cardiomyopathy, Dilated / blood*
  • Cardiomyopathy, Dilated / pathology
  • Cardiomyopathy, Hypertrophic / blood*
  • Cardiomyopathy, Hypertrophic / pathology
  • Cell Cycle Proteins / analysis
  • Cell Cycle Proteins / biosynthesis
  • Cell Line
  • Cytokines / analysis
  • Cytokines / biosynthesis*
  • Cytokines / blood
  • DNA-Binding Proteins / analysis
  • DNA-Binding Proteins / biosynthesis
  • Fanconi Anemia Complementation Group Proteins
  • Female
  • Humans
  • Interleukin-6 / biosynthesis
  • Interleukin-6 / blood
  • Male
  • Middle Aged
  • Myocardium / chemistry
  • Myocardium / metabolism
  • Myocardium / pathology
  • Nuclear Proteins / analysis
  • Nuclear Proteins / biosynthesis
  • Predictive Value of Tests
  • Proto-Oncogene Proteins c-bcl-2 / analysis
  • Proto-Oncogene Proteins c-bcl-2 / biosynthesis
  • Receptors, Interleukin-6 / biosynthesis
  • Receptors, Interleukin-6 / blood*
  • Signal Transduction / drug effects
  • Tumor Necrosis Factor-alpha / analysis
  • Tumor Necrosis Factor-alpha / biosynthesis
  • Tumor Necrosis Factor-alpha / pharmacology
  • bcl-2-Associated X Protein

Substances

  • Annexin A5
  • BAX protein, human
  • Cell Cycle Proteins
  • Cytokines
  • DNA-Binding Proteins
  • Fanconi Anemia Complementation Group Proteins
  • Interleukin-6
  • Nuclear Proteins
  • Proto-Oncogene Proteins c-bcl-2
  • Receptors, Interleukin-6
  • Tumor Necrosis Factor-alpha
  • bcl-2-Associated X Protein