Cellular mechanisms of GABAergic inhibition in neocortical dendrites
Cellular mechanisms of GABAergic inhibition in neocortical dendrites
批准号:
10054197
负责人:
Michael James Higley
金额:
$41.84万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-09-20 至 2022-10-31
关键词:
BiochemicalBrainCalciumCellsCellular biologyCharacteristicsDataDendritesDevelopmentDiseaseDisease modelElectrophysiology (science)EmbryoEpilepsyEquilibriumFunctional disorderGlutamate ReceptorGlutamatesGoalsHeterogeneityImageIndividualInhibitory SynapseInterneuronsInvestigationKnowledgeLabelLaser Scanning MicroscopyLinkLong-Term PotentiationMediatingMonitorN-MethylaspartateNeocortexNeurodevelopmental DisorderNeuronsPatternPeptidesPlayPopulationPrefrontal CortexProcessRegulationRoleSchizophreniaShapesSignal TransductionSomatostatinSourceSynapsesSynaptic plasticityautism spectrum disordercellular targetingexperienceexperimental studygamma-Aminobutyric Acidglutamatergic signalinghippocampal pyramidal neuronimaging studyinsightmature animalneocorticalnerve supplyneuropsychiatric disordernoveloptogeneticspostnatal periodpostsynapticresponsespatiotemporalsynaptogenesistooltwo-photonvoltage
中文摘要
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英文摘要
Project Summary
The development of excitatory and inhibitory circuits in the neocortex is critical for
establishing normal patterns of brain activity, and dysregulation of this process may contribute
to a number of neuropsychiatric disorders, including schizophrenia and autism. However, the
organization and regulation of inhibitory synaptogenesis during early development remain poorly
understood. This lack of knowledge is due, in part, to heterogeneity in GABAergic circuits and
the absence of appropriate tools for dissecting the contribution of different IN populations to
early GABAergic signaling. In the present study, we utilize a combination to electrophysiology,
optogenetics, 2-photon imaging and uncaging, and fluorescent labeling of GABAergic synapses
to (1) elaborate the development of functional inhibitory inputs to pyramidal neuron (PN)
dendrites, (2) reveal novel mechanisms for circuit-specific GABAergic plasticity, and (3)
elucidate the interactions of glutamatergic and GABAergic signaling in the normal wiring of
cortical circuits. Our overall goal is to understand the links between excitatory and inhibitory
signaling that operate during development and maintain cortical circuit function. We expect that
our results will generate new avenues for exploring both the cell biology of GABAergic function
and the general mechanisms by which the brain develops and adapts to experience.
期刊论文(0)
专著(0)
科研奖励(0)
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