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ParallelMemories

Cooperative and competitive parallel memory units for choice behaviors

Total Cost €

0

EC-Contrib. €

0

Partnership

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 ParallelMemories project word cloud

Explore the words cloud of the ParallelMemories project. It provides you a very rough idea of what is the project "ParallelMemories" about.

update    sparse    retrieve    axonal    plasticity    drivers    forms    reward    extensive    integrate    molecules    types    genetic    decay    predictive    anatomical    experiments    rate    manipulating    cells    write    synaptic    punishment    mechanisms    diverse    shown    circuit    form    flexibility    map    action    optogenetic    dopamine    mb    probe    associative    mushroom    cues    biological    stimuli    body    drosophila    cell    understand    downstream    event    neurons    rules    independently    manipulate    anatomically    units    guide    sensory    activation    competitively    insect    cooperatively    selectively    60    draw    brains    dynamics    matched    latest    learning    identity    functions    kenyon    center    store    16    fibers    capacity    compartmental    molecular    individual    parallel    imaging    output    model    associations    nearly    dopaminergic    differences    intersectional    underlying    storage    flies    activate    allowed    memory    memories   

Project "ParallelMemories" data sheet

The following table provides information about the project.

Coordinator
THE CHANCELLOR MASTERS AND SCHOLARSOF THE UNIVERSITY OF CAMBRIDGE 

Organization address
address: TRINITY LANE THE OLD SCHOOLS
city: CAMBRIDGE
postcode: CB2 1TN
website: www.cam.ac.uk

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 United Kingdom [UK]
 Total cost 1˙500˙000 €
 EC max contribution 1˙500˙000 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2017-STG
 Funding Scheme ERC-STG
 Starting year 2018
 Duration (year-month-day) from 2018-07-01   to  2023-06-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    THE CHANCELLOR MASTERS AND SCHOLARSOF THE UNIVERSITY OF CAMBRIDGE UK (CAMBRIDGE) coordinator 1˙500˙000.00

Map

 Project objective

This proposal seeks to understand the molecular and circuit mechanisms used to store information in parallel memory units, and how these memories are integrated to guide action selection. We will use the Drosophila mushroom body (MB), a key center for associative learning in insect brains, as a model system. We recently generated intersectional genetic drivers that allowed us to draw a comprehensive anatomical map and selectively manipulate nearly all of the MB’s ~60 cell types. Sparse activity in the 2,000 Kenyon cells of the MB represents the identity of sensory stimuli. Along the parallel axonal fibers of Kenyon cells, we have shown that dopaminergic neurons and MB output neurons form 16 matched compartmental units. These anatomically defined units are also units of associative learning: reward and punishment activate distinct subsets of dopaminergic neurons. Our latest optogenetic activation experiments demonstrate that individual dopaminergic neurons independently write and update memories in each unit with cell-type-specific rules. We find extensive differences in the rate of memory formation, decay dynamics, storage capacity and flexibility to learn new associations across different units. Thus individual memory units within the mushroom body store different information about the same learning event. Together, these memories cooperatively or competitively represent the predictive value of sensory cues. We will now identify molecules and cell biological features that enable dopamine neurons to produce diverse forms of synaptic plasticity underlying distinct learning rules in different memory units. We will anatomically identify downstream neurons of the mushroom body output neurons that integrate information from parallel memory units, and make genetic drivers for them. Then, we will probe functions of these downstream neurons by imaging or manipulating their activity while flies retrieve and integrate memories for action selection.

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