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IN-Fo-trace-DG SIGNED

Role of GABAergic interneurons in the formation of new memory traces in the Dentate Gyrus ofbehaving mice

Total Cost €

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EC-Contrib. €

0

Partnership

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 IN-Fo-trace-DG project word cloud

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assembly    progress    individual    environment    tools    molecular    mechanisms    disciplinary    memories    visualize    trace    cells    neuronal    neurons    interference    group    born    cellular    constraints    acquisition    recruitment    association    associations    ins    ones    interneurons    cell    time    examine    difficult    interconnectivity    temporal    emerge    unknown    gcs    excitatory    changing    networks    intensive    virtual    adapt    innovative    first    space    differently    discrete    suggest    dg    brain    area    signals    traces    despite    granule    analyze    modifications    patterns    cortical    fo    imaging    dentate    inhibitory    output    insights    populations    recordings    little    mature    made    gabaergic    fundamental    structure    population    adult    plasticity    question    principal    vivo    excitation    processed    theories    memory    organisms    balance    form    inhibition    photon    synapses    learning    optogenetic    gyrus    dependent    largely    spatial   

Project "IN-Fo-trace-DG" data sheet

The following table provides information about the project.

Coordinator
UNIVERSITAETSKLINIKUM FREIBURG 

Organization address
address: HUGSTETTER STRASSE 49
city: FREIBURG
postcode: 79106
website: n.a.

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country Germany [DE]
 Total cost 2˙463˙693 €
 EC max contribution 2˙463˙693 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2017-ADG
 Funding Scheme ERC-ADG
 Starting year 2018
 Duration (year-month-day) from 2018-10-01   to  2023-09-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    UNIVERSITAETSKLINIKUM FREIBURG DE (FREIBURG) coordinator 2˙463˙693.00

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 Project objective

Despite intensive study in the past on the problem of how information is processed in the brain to enable individual organisms to adapt to their continuously changing environment, little progress has been made on how new similar but discrete memory traces emerge in neuronal networks during learning. Current theories suggest that experience-dependent modifications in excitation-inhibition balance enable a selected group of neurons to form a new cell association during learning which represent the new memory trace. It was further proposed that particularly GABAergic inhibitory interneurons (INs) have a large impact on population activity in neuronal networks by means of their inhibitory output synapses. However, how cell associations emerge in space and time and how INs may contribute to this process is still largely unknown. This complex topic was so far difficult to address due to technical constraints. IN-Fo-Trace-DG aims to address this fundamental question in the dentate gyrus (DG), a brain structure essential for the acquisition of similar but discrete new memories. Based on our detailed knowledge on DG’s cellular elements, their interconnectivity and our recently established molecular interference tools, we will first, visualize the spatial and temporal activity patterns of cell populations during spatial learning in a virtual-reality using 2-Photon imaging. Second, we will determine the role of IN recruitment and plasticity in assembly formation by optogenetic and molecular interference. Third, we will analyze changes in excitatory and inhibitory signals in granule cells (GCs), the principal cells in this brain area, and INs during learning using whole-cell recordings in vivo. Finally, we will examine whether adult-born GCs contribute differently to learning-associated population activity compared to mature ones in the adult DG. This innovative multi-disciplinary approach will provide new insights on the mechanisms of new memory formation in cortical networks.

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