The role of cortical neuron and circuit function in tau induced neurodegeneration
The role of cortical neuron and circuit function in tau induced neurodegeneration
批准号:
8258751
负责人:
TIMOTHY JOEL CHERRY
金额:
$5.22万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-05-01 至 2013-04-30
关键词:
AffectAlzheimer&aposs DiseaseAutomobile DrivingBrainCalciumCell physiologyCellsCerebral cortexDefectDementiaDiseaseDyesErythrocytesEventFrontotemporal DementiaFunctional disorderGenesGoalsHousingHumanImageImpaired cognitionIndividualKnowledgeLeadLifeMediatingMolecularMusMutationNerve DegenerationNervous System PhysiologyNeuraxisNeurodegenerative DisordersNeurofibrillary TanglesNeuronal DysfunctionNeuronsNeurophysiology - biologic functionParalysedPathologyPick Disease of the BrainProcessResolutionRoleSensorySignal TransductionStimulusStructureSynapsesSystemTauopathiesTransgenic MiceVisual CortexWild Type MouseWorkabstractingarea striatacalcium indicatorcorticobasal degenerationdesignhyperphosphorylated tauimprovedin vivoinformation processingmouse modelmutantneural circuitneural patterningphotoactivationrelating to nervous systemresponsesensory stimulustau Proteinstau expressiontau mutationtooltransgene expressiontwo-photon
中文摘要
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英文摘要
Project Summary/Abstract:
Mutations in the gene encoding the microtubule associated protein tau can lead to devastating neurodegenerative diseases in humans. Previous studies in humans and mice have shown that synapse loss is one of the earliest events in tau-mediated neurodegeneration. Until recently however, it has been impossible to assess the effects of this synapse loss on the function of cells and circuits in the intact brain. The studies put forward in this proposal will: 1) determine how mutant tau expression affects the spontaneous and evoked activity of neurons within the mouse cerebral cortex, 2) characterize the consequences of mutant tau expression on cortical information processing, and 3) assess the dysfunction of local cortical circuits caused by mutant tau.
These studies will use in vivo two-photon imaging with calcium indicators to determine how synaptic defects lead to cellular and system-wide dysfunction in mouse models of tau-mediated disease. I anticipate that these studies will improve the current understanding of the initiating events of neurodegeneration and how neural activity is compromised in brains expressing mutant forms of tau.
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