Harnessing Adult Hippocampal Neurogenesis to Enhance Learning and Modulate Mood
Harnessing Adult Hippocampal Neurogenesis to Enhance Learning and Modulate Mood
批准号:
8324287
负责人:
Amar Sahay
金额:
$24.74万
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-08-01 至 2014-05-31
关键词:
AblationAddressAdultAdverse effectsAntidepressive AgentsAnxietyApoptosisAwardBehaviorBehavioralBiologicalBrainCellsChronicCognitionCognitive deficitsComplementCytoplasmic GranulesDevelopmentDiscrimination LearningElderlyEmotionsExerciseExhibitsFrightGeneticGoalsHippocampus (Brain)Impaired cognitionInstructionInterventionKruppel-like transcription factorsLearningLinkLiteratureMajor Depressive DisorderMediatingMediator of activation proteinMemoryMental DepressionMental disordersMolecular BiologyMoodsMusNeuronsNeurosciencesPatternPhasePhysiologyProcessPropertyResearchRoleStressSwimmingSynapsesSynaptic plasticityTestingTherapeuticTimeTrainingVertebral columnWorkadult neurogenesisbasebehavior measurementcell typeconditioned feardentate gyrusdesigndevelopmental neurobiologyexperiencefeedinggain of functionimprovedinsightmood regulationmouse modelnerve stem cellneurogenesisnovelresearch studytranscription factor
中文摘要
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英文摘要
The goal of this project is to understand how the plasticity of adult-born neurons may be harnessed to
modify learning and mood regulation. During the training phase (K99) of the award, the candidate
augmented his extensive background experience in developmental neurobiology, molecular biology and
mouse genetics with a rigorous training in behavioral neuroscience as applied to the study of cognition and
emotion in mice. The candidate employed a novel genetic gain of function approach to demonstrate the
impact of selectively increasing adult hippocampal neurogenesis on cognition and mood. In the
independent (ROO) phase, the candidate will explore the effects of manipulating the properties of adult-born
dentate granule neurons, rather than their number, on dentate gyrus dependent functions. The candidate
will build on recent work showing that the transcription factor Kruppel-like factor 9 regulates dentate granule
neuronal maturation. The Specific Aims will assess how genetic over expression of Kruppel-like factor 9 in
adult neural stem cells and dentate granule neurons influences their maturation and hippocampal functions
in normal mice and mouse models of depression. Although a growing literature documents the unique
properties of new neurons, how these properties of new neurons relate to fundamental mnemonic
processes such as pattern separation and the role of the dentate gyrus in mood regulation is poorly
understood. Therefore, the experiments proposed here will attempt to causally link discrete changes in
cell-type properties with circuit functions and behavior.
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依托单位:
Harnessing Adult Hippocampal Neurogenesis to Enhance Learning and Modulate Mood
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依托单位:
海外基金