METABOSTEM

METABOLIC CONTROL OF IMMATURE STROMAL CELL BIOLOGY

 Coordinatore CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE 

 Organization address address: Rue Michel -Ange 3
city: PARIS
postcode: 75794

contact info
Titolo: Dr.
Nome: Armelle
Cognome: Barelli
Email: send email
Telefono: 33561336080
Fax: 33562172901

 Nazionalità Coordinatore France [FR]
 Totale costo 75˙000 €
 EC contributo 75˙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-2011-CIG
 Funding Scheme MC-CIG
 Anno di inizio 2011
 Periodo (anno-mese-giorno) 2011-08-01   -   2014-07-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE

 Organization address address: Rue Michel -Ange 3
city: PARIS
postcode: 75794

contact info
Titolo: Dr.
Nome: Armelle
Cognome: Barelli
Email: send email
Telefono: 33561336080
Fax: 33562172901

FR (PARIS) coordinator 75˙000.00

Mappa


 Word cloud

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

regenerative    biology    metabolic    immature    compartment    metabostem    poorly    fate    mechanism    tissue    adipose    stromal    supporting    populations    cell    stem    asc    cells    population   

 Obiettivo del progetto (Objective)

'A very recent literature claims that metabolic status represents a crucial regulatory mechanism that helps direct stem cells fate. Whereas mainly described on the well characterized hematopoietic stem cells population, such metabolic investigations have been poorly conducted on another key population of adult immature cells that populate the stromal compartment of all tissues, i.e. the mesenchymal stromal/stem cells (MSC). Among them, adipose-derived stromal/stem cells (ASC) have been defined both as multipotent precursors and as supporting cells through their high secretory and immunomodulatory properties. These ASC hallmarks explain their potent regenerative capacities and have prompted clinical studies on their therapeutic potential. However, the mechanisms that govern their plasticity and fate as well as their interactions with other cell populations still remain to be unravelled. Along with ASC, adipose tissue harbours other immature populations whose biology is poorly described. The main objective of this METABOSTEM project is to investigate the role of metabolism in the intrinsic biology and fate of immature stromal populations residing within adipose tissue. Based on neuron-astrocyte and cancer cells models, we hypothesize that supporting cells such as ASC control the surrounding immature populations through a metabolic coupling, representing a new and primitive mechanism by which stromal compartment could control stem cells biology within the niche. This interdisciplinary project will integrate different scientific fields and techniques together such as in situ analysis, metabolic characterisation and stem cell biology, using murine adipose tissue as a working model. The METABOSTEM proposal will hopefully help at a better understanding of the biology of immature stromal cells from adipose tissue, both in physiological and regenerative conditions, and will have larger consequences on the way to manipulate and expand them.'

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