TRAPAMPAR

Role of lateral diffusion of AMPA Receptors in LTP

 Coordinatore UNIVERSITE VICTOR SEGALEN BORDEAUX II 

 Organization address address: RUE LEO SAIGNAT 146
city: BORDEAUX CEDEX
postcode: 33076

contact info
Titolo: Dr.
Nome: Daniel
Cognome: Choquet
Email: send email
Telefono: 33-5-57 57 40 90
Fax: 33-05 57 57 40 82

 Nazionalità Coordinatore France [FR]
 Totale costo 0 €
 EC contributo 167˙145 €
 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-IIF-2008
 Funding Scheme MC-IIF
 Anno di inizio 2010
 Periodo (anno-mese-giorno) 2010-03-01   -   2012-02-29

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    UNIVERSITE VICTOR SEGALEN BORDEAUX II

 Organization address address: RUE LEO SAIGNAT 146
city: BORDEAUX CEDEX
postcode: 33076

contact info
Titolo: Dr.
Nome: Daniel
Cognome: Choquet
Email: send email
Telefono: 33-5-57 57 40 90
Fax: 33-05 57 57 40 82

FR (BORDEAUX CEDEX) coordinator 167˙145.56

Mappa


 Word cloud

Esplora la "nuvola delle parole (Word Cloud) per avere un'idea di massima del progetto.

events    ampa    source    ltp    pool    ampar    extrasynaptic    activation    synaptic    newly    mobile    receptors    inserted   

 Obiettivo del progetto (Objective)

'Synaptic recruitment of AMPA receptors (AMPAR) is a critical step in synaptic plasticity events such as Long term potentiation (LTP). Although the signaling events necessary for the induction of LTP are well known (i.e. NMDA receptor activation and activation of protein kinase cascades), the source of the newly inserted AMPAR is still unclear. There are two pools of AMPA receptors that can be potentially mobilized to the synapse during LTP: a pool of AMPAR-containing intracellular vesicles and a pool of membrane-located extrasynaptic AMPAR. Since recent studies carried out mainly at the host laboratory have demonstrated that extrasynaptic AMPAR are highly mobile (sometimes moving in and out of synapses), it is possible that the increases in synaptic transmission observed during LTP might be due to the diffusional trapping of passing extrasynaptic AMPAR. During this project I will use a combination of state of the art imaging and electrophysiological approaches to test the hypothesis that mobile extrasynaptic AMPAR correspond to the most immediate source for the newly inserted AMPAR during LTP.'

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