Dynamics and molecular mechanism of synaptic connectivity change during learning
Dynamics and molecular mechanism of synaptic connectivity change during learning
批准号:
8745867
负责人:
Yi Zuo
金额:
$44.28万
依托单位国家:
美国
项目类别:
财政年份:
2014
资助国家:
美国
项目状态:
已结题
起止时间:
2014-09-05 至 2019-06-30
关键词:
AffectApicalAxonBiologyBoxingBrainDataDefectDendritesDendritic SpinesDevelopmentDissectionExcitatory SynapseFoundationsFutureGenerationsGoalsHumanImageImmunofluorescence ImmunologicIndividualInvestigationKnowledgeLabelLearningLifeMeasuresMemoryMental disordersMicroscopyModificationMolecularMolecular ProfilingMorphologyMotorMotor CortexMusNeuronal PlasticityNeuronsPathologyPathway interactionsPatternPopulationProcessProteinsProteomicsProxyResearchScanning Electron MicroscopySiteSpecificityStagingStructureSynapsesSynaptic plasticityTestingThalamic structureTrainingTranslational ResearchVertebral columncell typeexperiencehippocampal pyramidal neuronimaging modalityin vivoin vivo imaginginformation processinginnovationinsightmolecular dynamicsmolecular markermotor learningmotor skill learningnervous system disorderneural circuitnovelpostsynapticpreferencepresynapticprotein expressionprotein profilingpublic health relevancesynaptogenesistomographytooltwo-photon
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Synapses are the sites of information processing in the mammalian brain. While generation and persistence of synapses during learning make them potential substrate for circuit modification and memory storage, the molecular mechanisms underlying synaptic structural changes and synapse diversity remain to be elucidated. Dendritic spines are the postsynaptic sites for the majority of excitatory synapses in the brain. Using an innovative combination of in vivo two-photon imaging and retrospective Array Tomography, the goals of this proposal are to determine the molecular composition and local connectivity of learning-related synapses, and to reveal principles of circuit remodeling during learning. We propose three specific aims. Aim 1 examines the protein expression of individual spines (postsynaptic structures of excitatory synapses) during the process of synaptogenesis. Such expression patterns will be compared with those of preexisting stable spines to determine the molecular signature of new spines formed during learning. Aim 2 identifies the presynaptic partners for learning-associated new spines, and dissects how local circuits "reweigh" or "rewire" during learning. Aim 3 investigates how spine dynamics of pyramidal neurons from different cortical layers respond to motor learning, and determines if new spines formed during learning receive unique presynaptic inputs. Successful completion of the research will not only provide critical insights into the biology of synapse formation and diversity, but also offer neuroscientists a novel tool box to highlight new connections formed in a brain's recent past. Discovering how synapses remodel during learning will build a foundation for future investigation of how synaptic structure/function is altered by pathologies associated with learning defects.
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