KARTRAF

SYNAPTIC TRAFFICKING OF KAINATE RECEPTORS IN HIPPOCAMPAL CA3 PYRAMIDAL CELLS IN VIVO

 Coordinatore UNIVERSITE VICTOR SEGALEN BORDEAUX II 

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

contact info
Titolo: Dr.
Nome: Christophe
Cognome: Mulle
Email: send email
Telefono: +33 5 57 57 40 80
Fax: +33 5 57 57 40 82

 Nazionalità Coordinatore France [FR]
 Totale costo 0 €
 EC contributo 165˙444 €
 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-IEF-2008
 Funding Scheme MC-IEF
 Anno di inizio 2009
 Periodo (anno-mese-giorno) 2009-05-01   -   2011-04-30

 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: Christophe
Cognome: Mulle
Email: send email
Telefono: +33 5 57 57 40 80
Fax: +33 5 57 57 40 82

FR (BORDEAUX CEDEX) coordinator 165˙444.55

Mappa


 Word cloud

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

localization    kars    mechanisms    proper    subcellular    kainate    brain    trafficking    functions    cellular    glutamate    situation    synaptic    neurons    cells    molecular    techniques    receptors    cultures    regulation   

 Obiettivo del progetto (Objective)

'The proper function of neurotransmitters receptors is highly dependent on their precise subcellular localization in neurons. The molecular and cellular mechanisms that govern the synaptic localization of glutamate receptors both depend on the molecular structure of receptors and on interactions with cytoplasmic and extracellular proteins. These mechanisms have been widely studied using a variety of techniques applied to nonneuronal cells and to dissociated neurons in cultures. In contrast, our aim is to approach this question in an experimental situation which approximates polarized trafficking of receptors in an in vivo situation. Excitatory synaptic transmission in the mammalian brain is primarily mediated by ionotropic glutamate receptors (iGluRs) which fall into three classes: AMPA, NMDA and KARs. These ligand gated ion channels share common architecture, but display divergent functions. Kainate receptors have recently appeared to play an important role in the regulation of the activity of synaptic networks. Kainate receptors are involved in synaptic integration, in synaptic plasticity, in the regulation of neurotransmitter release and in the control of neuronal excitability. These functions require the proper subcellular localization of kainate receptors in specific functional domains of the neuron, necessitating complex cellular and molecular trafficking events. We will study the mechanisms that account for the highly restricted localization of kainate receptors (KARs) in the proximal dendrites of hippocampal CA3 pyramidal cells, at mossy fiber (MF) synapses. For this purpose, we will take advantage of a multidisciplinary integrated approach combining molecular and cellular tools (transgenic mice, organotypic cultures, biolistic transfection) with electrophysiological and imaging techniques.'

Introduzione (Teaser)

Communication between cells in the brain involves glutamate receptors. European scientists dissected the mechanism that controls proper localisation of glutamate receptors in the hippocampus.

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