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001-es BibID:BIBFORM014718
Első szerző:Hamdani, Nazha
Cím:More severe cellular phenotype in human idiopathic dilated cardiomyopathy compared to ischemic heart disease / Hamdani Nazha, Borbély Attila, Veenstra Sophie P. G. R., Kooij Viola, Vrydag Wim, Zaremba Ruud, Remedios Cris, Niessen Hans W. M., Michel Martin C., Paulus Walter J., Stienen Ger J. M., van der Velden Jolanda
Dátum:2010
ISSN:0142-4319
Tárgyszavak:Orvostudományok Elméleti orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
Megjelenés:Journal Of Muscle Research And Cell Motility. - 31 : 4 (2010), p. 289-301. -
További szerzők:Borbély Attila (1978-) (kardiológus) Veenstra, Sophie P. G. R. Kooij, Viola Vrydag, Wim Zaremba, Ruud Remedios, Cris Niessen, Hans W. M. Michel, Martin C. Paulus, Walter J. Stienen, Ger J. M. Velden, Jolanda, van der
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Intézményi repozitóriumban (DEA) tárolt változat
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001-es BibID:BIBFORM015092
Első szerző:Velden, Jolanda, van der
Cím:Functional effects of protein kinase C-mediated myofilament phosphorylation in human myocardium / van der Velden J., Narolska N. A., Lamberts R. R., Boontje N. M., Borbély A., Zaremba R., Bronzwaer J. G. F., Papp Z., Jaquet K., Paulus W. J., Stienen G. J.
Dátum:2006
ISSN:0008-6363
Megjegyzések:In human heart failure beta-adrenergic-mediated protein kinase A (PKA) activity is down-regulated, while protein kinase C (PKC) activity is up-regulated. PKC-mediated myofilament protein phosphorylation might be detrimental for contractile function in cardiomyopathy. This study was designed to reveal the effects of PKC on myofilament function in human myocardium under basal conditions and upon modulation of protein phosphorylation by PKA and phosphatases.METHODS: Isometric force was measured at different [Ca(2+)] in single permeabilized cardiomyocytes from non-failing and failing human left ventricular tissue. Basal phosphorylation of myofilament proteins and the influence of PKC, PKA, and phosphatase treatments were analyzed by one- and two-dimensional gel electrophoresis, Western immunoblotting, and ELISA.RESULTS: Troponin I (TnI) phosphorylation at the PKA sites was decreased in failing compared to non-failing hearts and correlated well with myofilament Ca(2+) sensitivity (pCa(50)). Incubation with the catalytic domain of PKC slightly decreased maximal force under basal conditions, but not following PKA and phosphatase pretreatments. PKC reduced Ca(2+) sensitivity to a larger extent in failing (DeltapCa(50)=0.19+/-0.03) than in non-failing (DeltapCa(50)=0.08+/-0.01) cardiomyocytes. This shift was reduced, though still significant, when PKC was preceded by PKA, while PKA following PKC did not further decrease pCa(50). Protein analysis indicated that PKC phosphorylated PKA sites in human TnI and increased phosphorylation of troponin T, while myosin light chain phosphorylation remained unaltered.CONCLUSION: In human myocardium PKC-mediated myofilament protein phosphorylation only has a minor effect on maximal force development. The PKC-mediated decrease in Ca(2+) sensitivity may serve to improve diastolic function in failing human myocardium in which PKA-mediated TnI phosphorylation is decreased.
Tárgyszavak:Orvostudományok Klinikai orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
Megjelenés:Cardiovascular Research. - 69 : 4 (2006), p. 876-887. -
További szerzők:Narolska, Nadiya A. Lamberts, Regis Boontje, Nicky M. Borbély Attila (1978-) (kardiológus) Zaremba, Ruud Bronzwaer, Jean G. F. Papp Zoltán (1965-) (kardiológus, élettanász) Jaquet, Kornelia Paulus, Walter J. Stienen, Ger J. M.
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