DIFFEBIMG

Differentiation dynamics in size-controlled embryoid bodies

 Coordinatore 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

 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-2009-RG
 Funding Scheme MC-IRG
 Anno di inizio 2010
 Periodo (anno-mese-giorno) 2010-07-01   -   2014-06-30

 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

Mappa

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 Word cloud

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regenerative    movement    basic    cardiomyocytes    types    immense    differentiation    embryonic    cell    eb    vitro    live    imaging    throughput    generation    stem    hepatocytes    treatment    dynamics    medicine    cells   

 Obiettivo del progetto (Objective)

'In-vitro differentiation of embryonic stem cells into defined cell types is a field of immense importance for both regenerative medicine and for basic understanding of development. Promising clinical uses include generation of hepatocytes for treatment of liver failure and generation of cardiac progenitor cells or cardiomyocytes for treatment of acute coronary disease. Embryoid bodies (EB's), three dimensional aggregates of differentiating embryonic stem cells, have been the method of choice for in-vitro differentiation into several cell types, including motor neurons, hepatocytes and cardiomyocytes.

I suggest a high-throughput live cell imaging approach for the study of EB differentiation dynamics. I will develop a microfluidic-based system for controlled EB formation, for generation and imaging of both uniform and variable size and shape EB’s. I will study correlates of specific cell fate differentiation and cell movement patterns by imaging large numbers of such systems, in conjunction with protein reporter and lineage tracing fluorescent constructs. I will focus on the conditions for appearance of cardiomyocytes: supporting cell types, spatial characteristics and signaling events. The project will enhance our basic understanding of cell movement and rules of differentiation during early development, and can lead to improved protocols of in-vitro differentiation.'

Introduzione (Teaser)

In vitro differentiation of embryonic stem cells is a field of immense importance for regenerative medicine. A high-throughput live cell imaging study allowed for better understanding of differentiation dynamics.

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