More severe cellular phenotype in human idiopathic dilated cardiomyopathy compared to ischemic heart disease

N. Hamdani, A. Borbely, S.P.G.R. Veenstra, V. Kooij, W. Vrydag, R. Zaremba, C. dos Remedios, H.W.M. Niessen, M.C. Michel, W.J. Paulus, G.J.M. Stienen, J. van der Velden

Research output: Contribution to journalArticleAcademicpeer-review

33 Citations (Scopus)

Abstract

Activation of the beta-adrenergic receptor (beta AR) pathway is the main mechanism of the heart to increase cardiac output via protein kinase A (PKA)-mediated phosphorylation of cellular target proteins, and perturbations therein may contribute to cardiac dysfunction in heart failure. In the present study a comprehensive analysis was made of mediators of the beta AR pathway, myofilament properties and cardiac structure in patients with idiopathic (IDCM; n = 13) and ischemic (ISHD; n = 10) cardiomyopathy in comparison to non-failing hearts (donor; n = 10) for the following parameters: beta AR density, G-coupled receptor kinases 2 and 5, stimulatory and inhibitory G-proteins, phosphorylation of myofilament targets of PKA, protein phosphatase 1, phospholamban, SERCA2a and single myocyte contractility. All parameters exhibited the expected alterations of heart failure, but for most of them the extent of alteration was greater in IDCM than in ISHD. Histological analysis also revealed higher collagen in IDCM compared to ISHD. Alterations in the beta AR pathway are more pronounced in IDCM than in ISHD and may reflect sequential changes in cellular protein composition and function. Our data indicate that cellular dysfunction is more severe in IDCM than in ISHD
Original languageEnglish
Pages (from-to)289-301
JournalJournal of muscle research and cell motility
Volume31
Issue number4
DOIs
Publication statusPublished - 2010

Cite this