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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. €

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Partnership

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 IN-Fo-trace-DG project word cloud

Explore the words cloud of the IN-Fo-trace-DG project. It provides you a very rough idea of what is the project "IN-Fo-trace-DG" about.

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

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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