COBRE: UNR: MOLECULAR PHYSIOL & REGULATION OF VOLUME SENSITIVE CHLORIDE CHANNEL
COBRE: UNR: MOLECULAR PHYSIOL & REGULATION OF VOLUME SENSITIVE CHLORIDE CHANNEL
批准号:
7959480
负责人:
Diana McCloskey
金额:
$22.57万
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-06-01 至 2010-05-31
关键词:
Action PotentialsAmino AcidsAnionsArrhythmiaCardiacCardiomyopathiesCardiovascular systemCell VolumesCellsCenters of Research ExcellenceChloride ChannelsComputer Retrieval of Information on Scientific Projects DatabaseCongestive Heart FailureDiseaseFundingGrantHeartHomeostasisHypertrophyInstitutionIon Channel ProteinMolecularMyocardial IschemiaPhosphorylationPhysiologicalPhysiologyProtein IsoformsProtein KinaseProteinsProteomicsRegulationResearchResearch PersonnelResourcesRoleSmooth Muscle MyocytesSourceStructure-Activity RelationshipTransgenic MiceUnited States National Institutes of Healthclinically significantinsightmemberprotein complexresearch studyvoltage
中文摘要
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英文摘要
This subproject is one of many research subprojects utilizing the
resources provided by a Center grant funded by NIH/NCRR. The subproject and
investigator (PI) may have received primary funding from another NIH source,
and thus could be represented in other CRISP entries. The institution listed is
for the Center, which is not necessarily the institution for the investigator.
COBRE Project 1 will study the molecular physiology and regulation of volume-regulated anion channels in the heart. The molecular mechanism of Cl- channel regulation is an important issue for understanding how cells regulate their volume and for understanding structure/function relationships of ion channel proteins in general. We previously proposed ClC-3, a member of the ClC superfamily of voltage-dependent Cl- channels, as a molecular candidate responsible for native volume-regulated outwardly rectifying anion channels (VSOACs) in cardiac and smooth muscle cells. The experiments proposed in this project will provide new insights into the role of phosphorylation by various protein kinases of amino terminus amino acids in the regulation of the two major ClC-3 isoforms, use transgenic mice to further examine the relationship between ClC-3 and native VSOACs and reveal their physiological role, and finally will use molecular and proteomic approaches to identify the major components and accessory proteins that constitute the native VSOAC multimeric protein complex. Since the activation of cardiac Cl- channels can produce significant effects on action potential duration and automaticity, and are key regulators of cell volume homeostasis, these channels have important clinical significance for several myocardial diseases, including cardiac arrhythmias, myocardial ischemia, congestive heart failure and hypertrophy. This project has significant potential of elucidating the normal physiological and possible pathophysiological role of volume-sensitive Cl- channels in the heart and cardiovascular system.
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COBRE: UNR: MOLECULAR PHYSIOL & REGULATION OF VOLUME SENSITIVE CHLORIDE CHANNEL
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批准号:7720382
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项目类别:
-
资助金额:$20.7万
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财政年份:2008
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负责人:Diana McCloskey
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依托单位:
COBRE: UNR: MOLECULAR PHYSIOL & REGULATION OF VOLUME SENSITIVE CHLORIDE CHANNEL
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批准号:7609790
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项目类别:
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资助金额:$23.5万
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财政年份:2007
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负责人:Diana McCloskey
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依托单位:
海外基金