CELESTIAL

Identification of molecular pathways underlying activity-dependent neuron-glia communication using in vitro microfluidic systems

 Coordinatore UNIVERSITE DE LAUSANNE 

 Organization address city: LAUSANNE
postcode: 1015

contact info
Titolo: Prof.
Nome: Roman
Cognome: Chrast
Email: send email
Telefono: +41 21 6925450
Fax: +41 21 6925455

 Nazionalità Coordinatore Switzerland [CH]
 Totale costo 184˙709 €
 EC contributo 184˙709 €
 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-2011-IIF
 Funding Scheme MC-IIF
 Anno di inizio 2012
 Periodo (anno-mese-giorno) 2012-10-01   -   2014-09-30

 Partecipanti

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

 Organization address city: LAUSANNE
postcode: 1015

contact info
Titolo: Prof.
Nome: Roman
Cognome: Chrast
Email: send email
Telefono: +41 21 6925450
Fax: +41 21 6925455

CH (LAUSANNE) coordinator 184˙709.40

Mappa


 Word cloud

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

cells    co    culture    glia    peripheral    function    structure    interactions    neurons    neuronal    nervous    glial    communication   

 Obiettivo del progetto (Objective)

'Interactions between neurons and glial cells underlie the normal development, structure and function of the nervous system. Perturbation of this communication occurs during injury, in acquired or hereditary neuropathic diseases of the central and peripheral nervous systems, and with ageing. However, the specific nature and the physiological significance of neuron-glia interactions remain largely unknown. We propose here the use of a microfluidic co-culture platform to characterize and investigate the role of non-synaptic responses of glial cells following stimulation of neuronal activity. In particular, we will co-culture neurons and glial cells of the peripheral nervous system, and monitor glia-specific changes at the transcriptome- and the secretome-levels, after manipulation of the electrical activity of neurons. We will subsequently interfere with the identified signaling pathways, and study effects on neuronal structure and function. Following this in vitro approach, we expect to identify potential mediators of the axon-glia communication and decipher their role in maintaining the nervous system integrity and function.'

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