Phosphorylation of cMyBP-C Modulates Cardiac Arrhythmias
Phosphorylation of cMyBP-C Modulates Cardiac Arrhythmias
批准号:
8763886
负责人:
Ramzi J Khairallah
金额:
$5.31万
依托单位国家:
美国
项目类别:
财政年份:
2013
资助国家:
美国
项目状态:
已结题
起止时间:
2013-09-30 至 2015-09-01
关键词:
ActinsAction PotentialsActomyosin AdenosinetriphosphataseAdrenergic AgentsAnimal ModelAnimalsArrhythmiaAtrial FibrillationBindingBinding ProteinsCaffeineCalciumCardiacCardiac DeathCardiac MyocytesCardiac MyosinsCell physiologyCellsCessation of lifeClinicalConsciousDepressed moodDevelopmentDiagnosisDoseElectrocardiogramEnvironmentEventFrequenciesGenesGoalsHeartHeart AtriumHeart failureHypertrophic CardiomyopathyHypertrophyImplantIncidenceInjuryInterdisciplinary StudyInvestigationIschemiaIsometric ExerciseIsoproterenolKineticsLeadLengthLinkMeasuresMentorsMethodsMicrofilamentsMolecularMonitorMovementMusMuscle CellsMutant Strains MiceMutationMyocardialMyocardiumMyosin ATPaseOrganPathogenesisPathologicPatientsPhenotypePhosphorylationPilot ProjectsPlayPrevalenceProteinsProtocols documentationPumpRecurrenceRegulationResistanceRoleSarcomeresStressStress TestsStructureTelemetryThick FilamentTransducersTransgenic AnimalsTransgenic MiceVentricularVentricular DysfunctionVentricular Premature ComplexesVentricular TachycardiaVertebral columnWorkadrenergicblebbistatinflexibilityheart rate variabilityimproved functioningin vivoinsightmyosin-binding protein Cnew therapeutic targetnovelnovel strategiesnovel therapeuticspressurepreventpublic health relevanceresearch studyresponseskeletalsubcutaneoussuccesssudden cardiac deathtool
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): A recurrent clinical hallmark of heart failure (HF) is the occurrence of arrhythmias, which contribute to the increased incidence of sudden cardiac death in HF patients and can in turn also lead to worsening HF. Despite the clear link between HF and arrhythmia, no applicable treatment has been identified specifically targeting these electrical abnormalities. The PI and his mentors have recently discovered that cardiac myosin binding protein c (cMyBP-C) phosphorylation might play a role in modulating calcium (Ca2+) handling in the heart. This can have profound implications in understanding the mechanism leading to arrhythmia during HF and might identify novel therapeutic strategies. Indeed, cMyBP-C phosphorylation is extensively phosphorylated in the healthy heart and severely depleted in HF, pathological hypertrophy, ischemic injury and atrial fibrillation. The planned investigation will exploit well established methods of assessing cardiac function in vivo, as well as develop and refine novel tools to further extend the in vivo findings into single isolated cardiac ventricuar myocytes. Work by the PI and his mentors has established several transgenic animal models that will be critical to study how cMyBP-C can lead to arrhythmogenesis, and show that mice harboring mutations preventing phosphorylation of cMyBP-C display severe arrhythmia and cardiac death following adrenergic stress. We hypothesize that cMyBP-C phosphorylation is necessary for proper Ca2+ handling in the myocardium. Therefore, the overall objectives of this proposal are to: 1) determine the propensity for arrhythmias in mice harboring mutations ablating (AllP-) or mimicking (AllP+) phosphorylation of cMyBP-C, 2) investigate the molecular causes of altered Ca2+ in isolated cardiomyocytes. The unique feature of the proposed work is the combination of in depth in vivo study and single cell experiments in a richly interactive environment with a strong record of success in such work. For the PI, the investigation nicely supports his long-term plan of conducting interdisciplinary research related to cardiac function, with the prospect of broadening our understanding of the pathogenesis of heart failure.
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Phosphorylation of cMyBP-C Modulates Cardiac Arrhythmias
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批准号:8596465
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项目类别:
-
资助金额:$5.39万
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财政年份:2013
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负责人:Ramzi J Khairallah
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依托单位:
海外基金