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Effect of sphingosine-1-phosphate on L-type calcium current and Ca(2+) transient in rat ventricular myocytes
EE. Egom, JS. Bae, R. Capel, M. Richards, Y. Ke, RB. Pharithi, V. Maher, P. Kruzliak, M. Lei,
Jazyk angličtina Země Nizozemsko
Typ dokumentu časopisecké články
NLK
ProQuest Central
od 1997-01-01 do Před 1 rokem
Medline Complete (EBSCOhost)
od 2011-01-01 do Před 1 rokem
Health & Medicine (ProQuest)
od 1997-01-01 do Před 1 rokem
- MeSH
- intracelulární signální peptidy a proteiny metabolismus MeSH
- kardiomyocyty metabolismus MeSH
- krysa rodu rattus MeSH
- lysofosfolipidy farmakologie MeSH
- proteinfosfatasa 2 metabolismus MeSH
- sfingosin analogy a deriváty farmakologie MeSH
- srdeční komory metabolismus MeSH
- vápník metabolismus MeSH
- vápníková signalizace účinky léků MeSH
- vápníkové kanály - typ L metabolismus MeSH
- zvířata MeSH
- Check Tag
- krysa rodu rattus MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
Modulation of Ca(2+) homoeostasis in cardiac myocytes plays a major role in beat-to-beat regulation of heart function. Previous studies suggest that sphingosine-1-phosphate (S1P), a biologically active sphingomyelin metabolite, regulates Ca(2+) handling in cardiac myocytes, but the underlying mechanism is unclear. In the present study, we tested the hypothesis that S1P-induced functional alteration of intracellular Ca(2+) handling includes the L-type calcium channel current (ICa,L) via a signalling pathway involving P21-activated kinase 1 (Pak1). Our results show that, in rat ventricular myocytes, S1P (100 nM) does not affect the basal activity of ICa,L but is able to partially reverse the effect of the β-adrenergic agonist Isoproterenol (ISO, 100 nM) on ICa,L. S1P (25 nM) also significantly prevents ISO (5 nM)-induced Ca(2+) waves and diastolic Ca(2+) release in these cells. Our further molecular characterisation demonstrates that Pak1 activity is increased in myocytes treated with S1P (25 nM) compared with those myocytes without treatment of S1P. By immunoprecipitation we demonstrate that Pak1 and protein phosphatase 2A (PP2A) are associated in ventricular tissue indicating their functional interaction. Thus the results indicate that S1P attenuates β-adrenergic stress-induced alteration of intracellular Ca(2+) release and L-type Ca(2+) channel current at least in part via Pak1-PP2A-mediated signalling.
Department of Pharmacology University of Oxford Oxford UK
Department of Physiology Anatomy and Genetics University of Oxford Oxford UK
Department of Physiology and Biophysics University of Illinois at Chicago Chicago USA
Heart Efficiency Unit Cardiology Department The Adelaide and Meath Hospital Tallaght Dublin Ireland
Citace poskytuje Crossref.org
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- $a Egom, Emmanuel Eroume-A $u Education Division, Department of Clinical Medicine, University of Dublin/Trinity College, Dublin, Ireland. egom@ectrs.ca. Egom Clinical and Translational Research Services Ltd, Halifax, NS, B3H 4R7, Canada. egom@ectrs.ca.
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- $a Effect of sphingosine-1-phosphate on L-type calcium current and Ca(2+) transient in rat ventricular myocytes / $c EE. Egom, JS. Bae, R. Capel, M. Richards, Y. Ke, RB. Pharithi, V. Maher, P. Kruzliak, M. Lei,
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- $a Modulation of Ca(2+) homoeostasis in cardiac myocytes plays a major role in beat-to-beat regulation of heart function. Previous studies suggest that sphingosine-1-phosphate (S1P), a biologically active sphingomyelin metabolite, regulates Ca(2+) handling in cardiac myocytes, but the underlying mechanism is unclear. In the present study, we tested the hypothesis that S1P-induced functional alteration of intracellular Ca(2+) handling includes the L-type calcium channel current (ICa,L) via a signalling pathway involving P21-activated kinase 1 (Pak1). Our results show that, in rat ventricular myocytes, S1P (100 nM) does not affect the basal activity of ICa,L but is able to partially reverse the effect of the β-adrenergic agonist Isoproterenol (ISO, 100 nM) on ICa,L. S1P (25 nM) also significantly prevents ISO (5 nM)-induced Ca(2+) waves and diastolic Ca(2+) release in these cells. Our further molecular characterisation demonstrates that Pak1 activity is increased in myocytes treated with S1P (25 nM) compared with those myocytes without treatment of S1P. By immunoprecipitation we demonstrate that Pak1 and protein phosphatase 2A (PP2A) are associated in ventricular tissue indicating their functional interaction. Thus the results indicate that S1P attenuates β-adrenergic stress-induced alteration of intracellular Ca(2+) release and L-type Ca(2+) channel current at least in part via Pak1-PP2A-mediated signalling.
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- $a Bae, James S H $u Department of Pharmacology, University of Oxford, Oxford, UK.
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- $a Ke, Yunbo $u Department of Physiology and Biophysics, University of Illinois at Chicago, Chicago, USA.
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- $a Pharithi, Rebabonye B $u Heart Efficiency Unit, Cardiology Department, The Adelaide and Meath Hospital, Tallaght, Dublin, Ireland.
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- $a Kruzliak, Peter $u Department of Chemical Drugs, Faculty of Pharmacy, University of Veterinary and Pharmaceutical Sciences, Palackeho tr 1946/1, 656 91, Brno, Czech Republic. kruzliakpeter@gmail.com.
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- $a Lei, Ming $u Department of Pharmacology, University of Oxford, Oxford, UK. ming.lei@pharm.ox.ac.uk.
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