Odor Memory Traces in the Mouse Olfactory Cortex
Odor Memory Traces in the Mouse Olfactory Cortex
批准号:
10520053
负责人:
Alexander Fleischmann
金额:
$35.73万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2018
资助国家:
美国
项目状态:
已结题
起止时间:
2018-12-01 至 2024-11-30
关键词:
Alzheimer&aposs DiseaseAlzheimer&aposs disease patientAnimalsAreaAxonBehaviorBehavioralBrainBrain DiseasesCellsChronicDataDesire for foodDetectionFrightGenesGeneticGleanGoalsHippocampusHumanImageLearningMemoryMemory LossMethodsMolecularMolecular AnalysisMusNeurobiologyNeurodegenerative DisordersNeuronsOdorsOlfactory CortexOlfactory LearningPredispositionPropertyReproductionShapesSmell PerceptionStimulusSystemTestingVisualizationWorkawakeconditioningexperienceexperimental studyfear memorygenetic approachinnovationinsightmemory encodingmemory recallneuralneural circuitneuromechanismolfactory bulbpiriform cortexpredictive modelingpromoterresponsetranscriptomicstwo-photon
中文摘要
点击翻译按钮获取中文摘要
英文摘要
Project Summary/Abstract
Learning and memory are fundamental brain functions, yet their underlying cellular and neural circuit
mechanisms remain poorly understood. Odor memories are exceptionally robust in humans and animals, of
outstanding importance for survival and reproduction, and highly susceptible to neurodegenerative disorders
including Alzheimer Disease. The olfactory (piriform) cortex, where odor perception is thought to first emerge,
has long been suggested to encode odor memories. However, the cellular substrates and circuit mechanisms
of olfactory learning are unknown. Our long-term goal is to understand the cellular and neural circuit
mechanisms of odor perception and memory. The objective of this proposal is to provide a mechanistic
cellular/molecular understanding of how odor memories are encoded and expressed. To achieve this objective
we have developed activity-based intersectional genetic approaches in mice that allow us to identify and
manipulate the activity of piriform neurons that were activated during olfactory learning. Our overall hypothesis
is that odors activate sparse, distributed and functionally diverse piriform neurons, whose activity is necessary
and sufficient for olfactory learning and memory. Aim 1: To determine how manipulating the activity of
odor memory trace cells alters behavior. We will use genetic tagging based on cFos promoter activity (“Fos-
tagging”) to visualize and manipulate the activity of piriform neurons that were activated during olfactory
learning. Our preliminary data provide strong evidence for the necessity of Fos-tagged piriform ensembles for
odor fear memory recall. Aim 2: To determine how learning alters the odor response properties of
piriform ensembles. We will perform chronic two-photon imaging of odor-evoked activity in awake, behaving
mice, before, during, and after aversive and appetitive olfactory conditioning. We will also selectively analyze
the response properties of Fos-tagged piriform neurons that are essential for fear odor memory recall. We will
test the hypothesis that olfactory learning selectively enhances the encoding of stimulus detection and
discriminability in neurons constituting an olfactory memory trace. Aim 3: To determine the molecular
identity and connectivity of olfactory memory trace cells. To drive behaviors, piriform ensembles must
convey odor information to downstream target areas. Using our previously identified set of marker genes and
single cell transcriptomics we will determine the molecular identities of piriform neurons that are activated
during learning, and we will trace their axonal projections. We will test the hypothesis that olfactory learning
facilitates functional connectivity of piriform cortex with task-relevant target areas. This project is innovative
because is combines state-of-the-art genetic, behavioral, imaging and molecular approaches to identify the
cellular and neural circuit substrates for olfactory learning and memory. It is significant because it will have a
strong impact on the understanding of the neurobiology of memory loss in Alzheimer Disease patients.
期刊论文(2)
专著(0)
科研奖励(0)
会议论文
DOI:
10.1523/jneurosci.0381-24.2024
发表时间:
2024-09-18
期刊:
JOURNAL OF NEUROSCIENCE
影响因子:
5.3
作者:
[Pierre,Andrea, Pham,Tuan, Fleischmann,Alexander]
通讯作者:
Fleischmann,Alexander
DOI:
10.7554/elife.65445
发表时间:
2021-07-22
期刊:
eLife
影响因子:
7.7
作者:
[Zeppilli S, Ackels T, Attey R, Klimpert N, Ritola KD, Boeing S, Crombach A, Schaefer AT, Fleischmann A]
通讯作者:
Fleischmann A
Gene regulatory network control of olfactory cortex cell type specification
-
批准号:10656692
-
项目类别:
-
资助金额:$49.97万
-
财政年份:2023
-
负责人:Alexander Fleischmann
-
依托单位:
Odor Memory Traces in the Mouse Olfactory Cortex
-
批准号:10307522
-
项目类别:
-
资助金额:$44.59万
-
财政年份:2018
-
负责人:Alexander Fleischmann
-
依托单位:
Odor Memory Traces in the Mouse Olfactory Cortex
-
批准号:10063985
-
项目类别:
-
资助金额:$44.59万
-
财政年份:2018
-
负责人:Alexander Fleischmann
-
依托单位:
Odor Memory Traces in the Mouse Olfactory Cortex - Supplement
-
批准号:10405361
-
项目类别:
-
资助金额:$23.93万
-
财政年份:2018
-
负责人:Alexander Fleischmann
-
依托单位:
国内基金
海外基金
新型F-18标记香豆素衍生物PET探针的研制及靶向Alzheimer's Disease 斑块显像研究
-
批准号:81000622
-
项目类别:青年科学基金项目
-
资助金额:20.0万元
-
批准年份:2010
-
负责人:梁胜
-
依托单位:
阿尔茨海默病(Alzheimer's disease,AD)动物模型构建的分子机理研究
-
批准号:31060293
-
项目类别:地区科学基金项目
-
资助金额:26.0万元
-
批准年份:2010
-
负责人:郭亚芬
-
依托单位:
跨膜转运蛋白21(TMP21)对引起阿尔茨海默病(Alzheimer'S Disease)的γ分泌酶的作用研究
-
批准号:30960334
-
项目类别:地区科学基金项目
-
资助金额:22.0万元
-
批准年份:2009
-
负责人:董贵成
-
依托单位: