ODORLEARNINGCIRCUIT

Sensory learning-induced changes of neuronal population activity in the olfactory bulb of awake mice

 Coordinatore UNIVERSITE DE GENEVE 

 Organization address address: Rue du General Dufour 24
city: GENEVE
postcode: 1211

contact info
Titolo: Prof.
Nome: Alan
Cognome: Carleton
Email: send email
Telefono: 41223795426
Fax: 41223795402

 Nazionalità Coordinatore Switzerland [CH]
 Totale costo 277˙296 €
 EC contributo 277˙296 €
 Programma FP7-PEOPLE
Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call FP7-PEOPLE-2013-IIF
 Funding Scheme MC-IIF
 Anno di inizio 2014
 Periodo (anno-mese-giorno) 2014-04-01   -   2016-03-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    UNIVERSITE DE GENEVE

 Organization address address: Rue du General Dufour 24
city: GENEVE
postcode: 1211

contact info
Titolo: Prof.
Nome: Alan
Cognome: Carleton
Email: send email
Telefono: 41223795426
Fax: 41223795402

CH (GENEVE) coordinator 277˙296.80

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population    learning    evoked    encoded    questions    mice    odor    ob    pattern    awake    cell    olfactory    neuronal   

 Obiettivo del progetto (Objective)

'How sensory information is encoded by neuronal population activity in the brain, and how the pattern of activity is reshaped by experience constitute the fundamental questions in neuroscience research. In the current project, ‘OdorLearningCircuit’, we will address these questions with the rodent olfactory bulb (OB) as a model system. Although the odor-evoked neuronal activity in the OB has been extensively studied, less is known about how the population activity of each cell type is spatially organized in the OB, and how the organization is modified when animals actively use odor information to optimize their behavior. In this project, we aim to tackle these important issues by a combination of cutting-edge techniques: we will deliver genetically encoded Ca2 indicators (GECIs) specifically to major types of neurons in the OB, and use 2-photon microscopy to map the neuronal population activity from awake mice performing an odor discrimination task under head-restrained condition. We will analyze how spatio-temporal pattern of odor-evoked population activity is dynamically remodeled in awake learning mice, at single-cell resolution and with cell-type distinction. The knowledge to be gained in the project will not only be important in the field of olfactory physiology, but also provide useful implications for understanding the general mechanisms underlying learning in other neural circuits.'

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