Somatic Ca2+ Signaling in CNS Neurons
Somatic Ca2+ Signaling in CNS Neurons
批准号:
7163756
负责人:
DONNA L GRUOL
金额:
$32.93万
依托单位国家:
美国
项目类别:
财政年份:
2004
资助国家:
美国
项目状态:
已结题
起止时间:
2004-01-01 至 2008-12-31
关键词:
AccountingBioinformaticsBiological MarkersBiologyCalciumCalcium SignalingCell LineageCell NucleusCell physiologyClassificationClinicalClinical MarkersCollectionConditionCoupledDendritesDevelopmentDiagnosisDiseaseDistant MetastasisGene ExpressionGenesHistopathologyImaging TechniquesIndividualInterventionIsotopically-Coded Affinity TaggingLimb structureLong-Term SurvivorsMalignant Bone NeoplasmMalignant NeoplasmsMass Spectrum AnalysisMembraneMesenchymal Stem CellsMethodsMolecularMolecular AnalysisMolecular ProfilingMutationNeoplasm MetastasisNeuronsNuclearNumbersOperative Surgical ProceduresOutcomePathway interactionsPatientsPeptidesPersonal SatisfactionPhenotypePlayPrimary NeoplasmPrognostic FactorPropertyProtein AnalysisProteinsProteomeRegulationResistanceRoleSamplingSignal PathwaySignal TransductionStagingSurvival RateSystemTechnologyTeenagersTestingTimeTranscriptVariantbonechemotherapyclinically relevantcomparativeimprovedinsightinterdisciplinary approachnovel therapeuticsosteosarcomaoutcome forecastprognosticprogramsprotein expressionresearch studyresponsetherapeutic targettooltranscription factortumortumorigenesis
中文摘要
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英文摘要
DESCRIPTION (provided by applicant):
Neuronal activity produces dynamic changes in cellular calcium that play a central role in the regulation of a number of cellular functions including gene expression. Recently we demonstrated that early developing cerebellar Purkinje neurons express a membrane-to-nucleus somatic calcium signaling pathway that is driven by endogenously generated electrical activity at a developmentally significant stage, just prior to dendritic expression. Our preliminary results show that activation of this signaling pathway produces cytosolic and nuclear calcium signals and that these signals result in activation of transcription factors and changes in the level of downstream cellular proteins. We hypothesize that the endogenously generated activity that drives this pathway in the immature Purkinje neurons is a developmentally relevant signal and that one role for the activity is to induce changes in gene expression necessary for initiation of the next developmental stage, expression of functional dendrites. As a first step toward testing this hypothesis, we will apply gene array microanalysis to acutely isolated Purkinje neurons subjected to various stimulation paradigms at the relevant developmental stage. This approach will enable us to simultaneously analyze the effects of neuronal activation on a large number of neuronal transcripts known to contribute to neuronal function and development. By using this information in combination with analysis of protein expression and functional analysis using electrophysiological and calcium imaging techniques we will be able to gain an understanding of the impact of calcium-regulated gene expression at a specific developmental stage. We will also identify the molecular components and functional properties of the membrane-to-nucleus somatic calcium signaling pathway and determine the conditions that are essential for gene expression of proteins identified by the gene array microanalysis. Results from these studies will be directly relevant to the developmental program of Purkinje neurons, which has been well characterized on a morphological level and involves distinct and identifiable developmental stages. However, the general principles identified by the studies will also contribute significantly to our understanding of the role of activity-dependent gene expression during development in other CNS neuronal types.
期刊论文(5)
专著(0)
科研奖励(0)
会议论文
L-type Ca2+ channels contribute to current-evoked spike firing and associated Ca2+ signals in cerebellar Purkinje neurons.
L 型 Ca2 通道有助于小脑浦肯野神经元中电流诱发的尖峰放电和相关 Ca2 信号。
DOI:
10.1080/14734220600719692
发表时间:
2006
期刊:
Cerebellum (London, England)
影响因子:
--
作者:
[Gruol,DL, Netzeband,JG, Schneeloch,J, Gullette,CE]
通讯作者:
Gullette,CE
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