RETROGRADE SIGNALING

Molecular Mechanisms of Neurodegeneration

Coordinatore	TEL AVIV UNIVERSITY    more  Organization address address: RAMAT AVIV city: TEL AVIV postcode: 69978 contact info Titolo: Ms. Nome: Lea Cognome: Pais Email: send email Telefono: 97236408774 Fax: 97236409697
Nazionalità Coordinatore	Israel [IL]
Totale costo	100˙000 €
EC contributo	100˙000 €
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-2010-RG
Funding Scheme	MC-IRG
Anno di inizio	2011
Periodo (anno-mese-giorno)	2011-03-01   -   2015-02-28

 Partecipanti

#	participant	country	role	EC contrib. [€]
1	TEL AVIV UNIVERSITY  Organization address address: RAMAT AVIV city: TEL AVIV postcode: 69978 contact info Titolo: Ms. Nome: Lea Cognome: Pais Email: send email Telefono: 97236408774 Fax: 97236409697	IL (TEL AVIV)	coordinator	100˙000.00

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 Obiettivo del progetto (Objective)

'Neuron cell death and synapse disruption seen during aging and in neurodegenerative diseases is a non-cell-autonomous process and involve a multi system progression. As neurons are highly polarized cells with very long axons, in order to remain healthy and function properly, they depend on accurate and efficient long-distance communication mechanisms. My long-term goal is to elucidate the molecular mechanisms for long distance signaling between neurons and their environment. I will combine state-of-the-art multidisciplinary approaches such as single molecule live imaging techniques, nanofluid-co-culture chambers and differential proteomics approaches on mouse model systems to address basic questions on the roles that retrograde signaling between muscle, glia and neurons play in cell survival and synapse stability. We will develop a unique in vitro microfluidic platform with motor neuron cell bodies on one-side and glia/muscle cells on the other side, which will allow us to distinguish local versus long distance signaling mechanisms and monitor retrograde axonal transport, as well as to manipulate retrograde signaling pathway regulating NMJ maintenance and cell survival. Three approaches will be taken: 1. In vitro and in vivo live cell imaging. 2. Specific cell biology. 3. Functional proteomics. Using model systems for aging and for neurodegenerative diseases will allow us to characterize the vital signaling mechanisms for NMJ/synapse maintenance and neuronal survival, as well as reveal novel stress factors that lead to nerve degeneration and cell death. Using the above strategies will provide a clearer picture of how cells use spatial localization and transport to regulate cell survival and synapse stability. The research will generate novel insights into neurodegenerative mechanisms and, ultimately, provide a molecular basis for new drugs as well as delivery methods to treat a range of neurodegenerative diseases.'