DISTINCTIVE SPATIOTEMPORAL MAP OF TARGET ACTIVATION BY YOUNG NEURONS OF THE ADULT
DISTINCTIVE SPATIOTEMPORAL MAP OF TARGET ACTIVATION BY YOUNG NEURONS OF THE ADULT
批准号:
8505342
负责人:
FRED H GAGE
金额:
$4.98万
依托单位国家:
美国
项目类别:
财政年份:
2011
资助国家:
美国
项目状态:
已结题
起止时间:
2011-01-01 至 2015-06-30
关键词:
AcuteAddressAdultAnimalsAreaAstrocytesAwarenessAxonBiologicalBrainCationsCellsCharacteristicsCollaborationsCommunitiesDataDefectDevelopmentDevelopmental ProcessDiseaseDistalDyesFeedbackFemaleFrequenciesFutureGenerationsGlutamatesGoalsGrantGrowthHilarHippocampus (Brain)In VitroInfectionInstitutesInstitutionInstructionInternationalInterneuronsJointsKnowledgeLaboratoriesLearningLightLong-Term PotentiationMapsMediatingMemoryMental DepressionMolecularMorphologyMusNatural regenerationNerve DegenerationNeurodegenerative DisordersNeuronal DifferentiationNeuronsNewborn InfantOutcomeOutputPerinatalPhysiologic pulsePopulationPresynaptic TerminalsProcessPropertyProtein FamilyPyramidal CellsResearchResearch PersonnelRetroviral VectorRoleShapesSignal PathwaySignal TransductionSliceSocietiesSolidSourceStagingStimulusSynapsesTechnologyTestingTheoretical modelTimeTrainingTraumaUnited States National Institutes of HealthWhole-Cell Recordingsadult neurogenesisbrain repaircomputerized data processingdentate gyrusdesigndriving forceexpectationfeedinggamma-Aminobutyric Acidgranule cellhippocampal pyramidal neuronimprovedin vivoinformation processinglearned behaviorloss of functionmembermossy fibernerve stem cellneurogenesisneuron developmentnewborn neuronnovelparent grantpostsynapticpresynapticreconstructionregenerative therapyresponseretroviral transductionspatiotemporalsuccesssynaptogenesistooltransmission processyoung adult
中文摘要
成人齿状回不断产生特异性所需的颗粒细胞(DGCs)
英文摘要
The adult dentate gyrus continuously generates granule cells (DGCs) that are needed for specific
learning and memory tasks, but the precise contribution of new neurons to information processing in
the hippocampal circuitry remains unknown. In the past, we have demonstrated that key
developmental processes occurring in the perinatal brain such as maturation of excitability, afferent
synaptogenesis and function are all recapitulated during adult neurogenesis. We now propose the
central hypothesis that newly born cells establish functional outputs as they develop, and the
population of postsynaptic target cells contacted by young neurons is predominantly inhibitory,
therefore different from the mixed excitatory/inhibitory network activated by mature granule cells.
Thus, there would be a time window in which young DGCs primarily activate feedforward and/or
feedback inhibitory circuits without exciting pyramidal cells, exerting a tight inhibitory control over
the dentate gyrus output. In Aim 1 we will build a spatio-temporal map of target activation by young
developing neurons of the adult dentate gyrus. We will use retroviral transduction to express the light-
activated cation channel Channelrhodopsin-2 in newborn DGCs of young-adult female mice
(C57Bl6/J). We will sacrifice the animals at different times and prepare acute brain slices to carry out
electrophysiological recordings. By stimulating the whole hippocampal slice with brief light pulses, all
retrovirally transduced neurons will spike. We will search randomly for active postsynaptic target cells
throughout the hilus and CA3 regions, and identify and characterize responsive neurons by combining
loose patch and whole-cell recordings. In Aim 2 we will investigate the functional maturation of new
mossy fiber synapses made onto GABAergic and glutamatergic targets. We plan to utilize whole-cell
recordings to test whether synapses forming onto GABAergic interneuron targets mature faster than
those made onto pyramidal cells, as suggested by our previous structural studies. We will also study
presynaptic mechanisms of short- and long-term plasticity that will shape both activity-dependent
competition and activation of postsynaptic circuits. This project will address fundamental questions
about connectivity and activation (spiking) of newborn cells that will contribute to understanding the
precise impact of adult neurogenesis in the preexisting hippocampal network and the rules of neuronal
connectivity in the adult brain. Identifying the rules by which neurons integrate in the existing
network in a manner that is both safe and functionally relevant is also crucial for developing future
brain repair therapies.
Novel retroviral tools will be developed in collaboration with the Gage lab to enhance
Channelrhodopsin-2 expression, thus improving the capability of light activation of newborn cells. In
turn, experimental data obtained here will be used to feed into the theoretical model being developed
by the Gage lab on the role of immature neurons in signal processing. The success of the proposed
project relies on strengthening the close interaction between the Schinder laboratory at the Leloir
Institute (Buenos Aires) and the Gage laboratory at the Salk Institute of La Jolla. Members of the
Schinder lab will have the opportunity to train at Salk on the generation and characterization of novel
retroviral vectors, improving the capabilities to develop advanced molecular tools at the foreign
institution. We anticipate that capacity building leading to the design, generation and
use of novel retroviral tools at the Leloir Institute will have an enormous impact on the
local scientific community. This collaborative effort will therefore serve as a driving
force to increase the critical mass of Argentine investigators that incorporate
competitive technologies for the study of neurodegenerative disorders within their
research focus. An increase in the number of laboratories carrying out regeneration-
related projects will certainly enhance awareness to these and related problems to our
community.
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DOI:
10.1126/science.1214956
发表时间:
2012-03-09
期刊:
Science (New York, N.Y.)
影响因子:
--
作者:
[Marín-Burgin A, Mongiat LA, Pardi MB, Schinder AF]
通讯作者:
Schinder AF
DOI:
10.1016/j.mcn.2013.07.003
发表时间:
2013-09
期刊:
MOLECULAR AND CELLULAR NEUROSCIENCE
影响因子:
3.5
作者:
[Morgenstern, Nicolas A., Giacomini, Damiana, Lombardi, Gabriela, Castano, Eduardo M., Schinder, Alejandro F.]
通讯作者:
Schinder, Alejandro F.
DOI:
10.1523/jneurosci.1380-11.2011
发表时间:
2011-05-25
期刊:
The Journal of neuroscience : the official journal of the Society for Neuroscience
影响因子:
--
作者:
[Piatti VC, Davies-Sala MG, Espósito MS, Mongiat LA, Trinchero MF, Schinder AF]
通讯作者:
Schinder AF
DOI:
10.1016/j.neuron.2014.11.023
发表时间:
2015-01-07
期刊:
NEURON
影响因子:
16.2
作者:
[Temprana, Silvio G., Mongiat, Lucas A., Yang, Sung M., Trinchero, Mariela F., Alvarez, Diego D., Kropff, Emilio, Giacomini, Damiana, Beltramone, Natalia, Lanuza, Guillermo M., Schinder, Alejandro F.]
通讯作者:
Schinder, Alejandro F.
DOI:
10.1016/j.conb.2015.06.002
发表时间:
2015-12
期刊:
Current opinion in neurobiology
影响因子:
5.7
作者:
[Kropff E, Yang SM, Schinder AF]
通讯作者:
Schinder AF
Neuronal senescence and inflammation in Alzheimer's disease
-
批准号:10213563
-
项目类别:
-
资助金额:$142.5万
-
财政年份:2021
-
负责人:FRED H GAGE
-
依托单位:
Neuronal senescence and inflammation in Alzheimer's disease
-
批准号:10633023
-
项目类别:
-
资助金额:$7.45万
-
财政年份:2021
-
负责人:FRED H GAGE
-
依托单位:
Core 1: Human Cell Models of Aging Core
-
批准号:10410540
-
项目类别:
-
资助金额:$35.48万
-
财政年份:2020
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负责人:FRED H GAGE
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依托单位:
Core 1: Human Cell Models of Aging Core
-
批准号:10264817
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项目类别:
-
资助金额:$33.09万
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财政年份:2020
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负责人:FRED H GAGE
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依托单位:
Core 1: Human Cell Models of Aging Core
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批准号:10665581
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资助金额:$46.77万
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财政年份:2020
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负责人:FRED H GAGE
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依托单位:
Core 1: Human Cell Models of Aging Core
-
批准号:10045536
-
项目类别:
-
资助金额:$34.36万
-
财政年份:2020
-
负责人:FRED H GAGE
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依托单位:
Assessing cellular aging in old and rejuvenated neurons from Alzheimer patients
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批准号:10522910
-
项目类别:
-
资助金额:$116.96万
-
财政年份:2017
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负责人:FRED H GAGE
-
依托单位:
Assessing cellular aging in old and rejuvenated neurons from Alzheimer patients
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批准号:10835760
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项目类别:
-
资助金额:$21.27万
-
财政年份:2017
-
负责人:FRED H GAGE
-
依托单位:
Combinatorial Actions of Genetic Variants and Gender Bias of Alzherimer's Disease
-
批准号:9431031
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项目类别:
-
资助金额:$161.48万
-
财政年份:2017
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负责人:FRED H GAGE
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依托单位:
Assessing cellular aging in old and rejuvenated neurons from Alzheimer patients
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批准号:10153611
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项目类别:
-
资助金额:$48.5万
-
财政年份:2017
-
负责人:FRED H GAGE
-
依托单位:
Assessing cellular aging in old and rejuvenated neurons from Alzheimer patients
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批准号:9361030
-
项目类别:
-
资助金额:$48.5万
-
财政年份:2017
-
负责人:FRED H GAGE
-
依托单位:
Dynamics of activity-induced transcription in single dentate granule cells
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批准号:10191046
-
项目类别:
-
资助金额:$48.5万
-
财政年份:2017
-
负责人:FRED H GAGE
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依托单位:
ConProject-002
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批准号:10675215
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项目类别:
-
资助金额:$5.43万
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财政年份:2017
-
负责人:FRED H GAGE
-
依托单位:
ConProject-001
-
批准号:10675214
-
项目类别:
-
资助金额:$111.53万
-
财政年份:2017
-
负责人:FRED H GAGE
-
依托单位:
Assessing cellular aging in old and rejuvenated neurons from Alzheimer patients
-
批准号:9926786
-
项目类别:
-
资助金额:$48.5万
-
财政年份:2017
-
负责人:FRED H GAGE
-
依托单位:
Combinatorial Actions of Genetic Variants and Gender Bias of Alzherimer's Disease
-
批准号:10207441
-
项目类别:
-
资助金额:$150.13万
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财政年份:2017
-
负责人:FRED H GAGE
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依托单位:
Project 4: Consequences of Retrotransposable Element Activation in the Central Nervous System
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批准号:10581545
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项目类别:
-
资助金额:$60.67万
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财政年份:2016
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依托单位:
iPSC-based platform development for major psychiatric disorder modeling and discovery
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批准号:10247954
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-
资助金额:$18.91万
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财政年份:2016
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依托单位:
Project 4: Consequences of Retrotransposable Element Activation in the Central Nervous System
-
批准号:10333664
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-
资助金额:$62.09万
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财政年份:2016
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负责人:FRED H GAGE
-
依托单位:
iPSC-based platform development for major psychiatric disorder modeling and discovery
-
批准号:9983159
-
项目类别:
-
资助金额:$259.4万
-
财政年份:2016
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依托单位:
海外基金