Circadian Rhythm In Cone Photoreceptors: Cellular Mechanisms
Circadian Rhythm In Cone Photoreceptors: Cellular Mechanisms
批准号:
7768391
负责人:
GLADYS Y KO
金额:
$28.33万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-04-01 至 2012-02-29
关键词:
1-Phosphatidylinositol 3-KinaseActinsAge related macular degenerationBlindnessCalcium ChannelCell membraneCellular biologyCessation of lifeCharacteristicsCircadian RhythmsCyclic AMPCyclic AMP-Dependent Protein KinasesCyclic GMPCytoskeletonDNA Sequence RearrangementDataDefectDevelopmentDiseaseElderlyElementsEventFutureGated Ion ChannelGene ExpressionGenesGoalsHumanImageInstitutesKnowledgeL-Type Calcium ChannelsLeadLegal BlindnessMEKsMacular degenerationMediatingMedicalMelatoninMitogen-Activated Protein KinasesMolecularMovementMutationNeuronsNight BlindnessOutputPathogenesisPathway interactionsPeriodicityPhasePhosphatidylinositide 3-Kinase InhibitorPhosphatidylinositolsPhosphotransferasesPhotoreceptorsPhysiologyPlayProteinsRegulationResearchResearch PersonnelRetinaRetinal ConeRetinal DegenerationRetinal DiseasesReverse Transcriptase Polymerase Chain ReactionRoleSignal PathwaySignal TransductionSomatostatinStreamTechniquesTimeTransfectionUnited StatesVisionVisual impairmentWestern BlottingWorkbasecalmodulin-dependent protein kinase IIcircadian pacemakerdensityfovea centralisimmunocytochemistryinhibitor/antagonistmaculameetingsneurotransmissionneurotransmitter releasenovelpatch clamppreventprogramsprotein expressionprotein transportvoltage
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Macular degeneration is a major cause of visual impairment in the United States and is associated with the death of cone photoreceptors. The pathogenesis and the cellular events responsible for the distortion of central vision in macular degeneration are not understood. Circadian oscillators in retina photoreceptors are known to play important roles in regulating photoreceptor function and physiology, and disruption of these circadian oscillators leads to the death of photoreceptors and could contribute to the pathogenesis of macular degeneration. The objective of the proposed research is to elucidate the signaling pathways from the circadian oscillators leading to the regulation of L-type voltage-dependent calcium channels (VDCCs) in cone photoreceptors, since the L-type VDCCs are essential in regulating neurotransmitter release in the retina. For example, mutation of the L-type VDCC a1f subunit gene causes incomplete congenital stationary night blindness in humans, with a defect in neurotransmission between photoreceptors and second-order neurons. An integrative approach with multiple techniques including electrophysiological patch-clamp recordings, Western immunoblotting, immunocytochemistry with confocal imaging, quantitative real-time RT- PCR and gene transfection, will be used in this application to achieve the following four specific aims: Specific Aim 1. Characterize the circadian rhythmicity of VDCCs in chick cone photoreceptors. The circadian rhythmicity of L-type VDCCs at multiple time points throughout the entire circadian day will be characterized in detail. Specific Aim 2. Identify the cellular signaling pathways underlying the circadian regulation of VDCCs. The roles of PKA, MAP kinase, CaMKII and PI3 kinase as output pathways leading to the circadian regulation of VDCCs will be determined. Specific Aim 3. Elucidate the roles of actin cytoskeleton rearrangement and protein trafficking on circadian regulation of VDCCs. Specific Aim 4. Define the cellular mechanisms of the phase-dependent modulation of VDCCs by somatostatin. While somatostatin serves as a VDCC inhibitor in other neurons, it shows both phase-dependent enhancement and inhibition of L-type VDCCs in cones. This project will be among the very first studies to define the circadian regulation of L-type VDCCs and their molecular mechanisms in retina photoreceptors. Understanding the molecular signaling of circadian regulation of retina function may ultimately provide knowledge for developing new strategies to treat retinal diseases, especially age-related macular degeneration, and preventing blindness in the future, which are the long-term goals of the PI.
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会议论文
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Circadian Rhythm In Cone Photoreceptors: Cellular Mechanisms
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批准号:8035294
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资助金额:$27.2万
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Circadian Rhythm In Cone Photoreceptors: Cellular Mechanisms
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批准号:7384427
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资助金额:$27.81万
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资助金额:$36.23万
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Circadian Rhythm In Cone Photoreceptors: Cellular Mechanisms
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项目类别:
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资助金额:$28.62万
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财政年份:2007
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负责人:GLADYS Y KO
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依托单位:
Circadian Rhythm In Cone Photoreceptors: Cellular Mechanisms
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批准号:7197408
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项目类别:
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资助金额:$27.63万
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财政年份:2007
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负责人:GLADYS Y KO
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依托单位:
CIRCADIAN REGULATION OF CGMP-GATED ION CHANNELS
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批准号:6555833
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项目类别:
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资助金额:$5.21万
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财政年份:2002
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负责人:GLADYS Y KO
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依托单位:
CIRCADIAN REGULATION OF CGMP-GATED ION CHANNELS
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批准号:6659740
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项目类别:
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资助金额:$4.78万
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财政年份:2002
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负责人:GLADYS Y KO
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依托单位:
CIRCADIAN REGULATION OF CGMP-GATED ION CHANNELS
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项目类别:
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资助金额:$4.56万
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财政年份:2001
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依托单位:
海外基金