DYNACA-DA

Dynamic Calcium Clamp: Design and Applications

 Coordinatore UNIVERSITE PARIS DESCARTES 

 Organization address address: Rue de l'Ecole de Medecine 12
city: PARIS
postcode: 75270

contact info
Titolo: Dr.
Nome: Pierre-Paul
Cognome: Vidal
Email: send email
Telefono: -227
Fax: -228

 Nazionalità Coordinatore France [FR]
 Totale costo 230˙963 €
 EC contributo 230˙963 €
 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-2007-4-1-IOF
 Funding Scheme MC-IOF
 Anno di inizio 2008
 Periodo (anno-mese-giorno) 2008-10-01   -   2011-09-30

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    UNIVERSITE PARIS DESCARTES

 Organization address address: Rue de l'Ecole de Medecine 12
city: PARIS
postcode: 75270

contact info
Titolo: Dr.
Nome: Pierre-Paul
Cognome: Vidal
Email: send email
Telefono: -227
Fax: -228

FR (PARIS) coordinator 0.00

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 Word cloud

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cell    velocity    dynamic    mechanisms    synaptic    microscopy    host    tool    signal    calcium    variations    first    day    neurons    position    university    clamp    life    ca    eye    dynamics    time    laboratory    dendritic   

 Obiettivo del progetto (Objective)

'Calcium ion (Ca2) is one of the most important divalent ions in the day-to-day life of any cell, as shown by its involvement as second messenger in virtually all cell types, from life onset to cell death through almost every physiological processes (muscle contraction, heart physiology, coagulation, immune system control, neuronal information processing). Ca2 concentration can vary by up to 6 orders of magnitude with dynamics in the millisecond range; however, the investigation of its variations has been hindered by the lack of precise control over the dynamics, especially in excitable cells such as neuron. In this project, we propose to first build a new tool to control in real time the variations of intracellular Ca2 via the combination of two-photon microscopy and dynamic current clamp: the dynamic calcium clamp. Then, we propose to use this tool to investigate two neurophysiological mechanisms: one related to a new form of synaptic plasticity dependent on the rates of activity of both the pre and post synaptic neurons and the other to the integration of the eye velocity signal into an eye position signal. The conception of the dynamic calcium clamp and its first applications would be undertaken in Boston University, USA, since in this institution hosts both one of the leading laboratory in microscopy applied to Neurosciences (BioMicroscopy Lab, outgoing host) and a laboratory developing one of the best dynamic clamp software (NDL, partner). The last part of the project will be lead at the return host, located in Paris 5 University, FRANCE (LNRS-UMR7060). There, the dendritic properties of the neurons of the velocity to position integrator would be studied, with a special focus on the Goldman hypothesis about dendritic hysteresis which would modify the local computing properties. Thus, this project will at the same time provide new tools, better understanding of brain mechanisms and foster the development of the career of the fellow in Europe.'

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