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Defining the cellular dynamics leading to tissue expansion

 Coordinatore UNIVERSITE LIBRE DE BRUXELLES 

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 Nazionalità Coordinatore Belgium [BE]
 Totale costo 2˙399˙999 €
 EC contributo 2˙399˙999 €
 Programma FP7-IDEAS-ERC
Specific programme: "Ideas" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call ERC-2013-CoG
 Funding Scheme ERC-CG
 Anno di inizio 2014
 Periodo (anno-mese-giorno) 2014-06-01   -   2019-05-31

 Partecipanti

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

 Organization address address: Avenue Franklin Roosevelt 50
city: BRUXELLES
postcode: 1050

contact info
Titolo: Prof.
Nome: Cedric
Cognome: Blanpain
Email: send email
Telefono: +322 5554175
Fax: +32 2 5554655

BE (BRUXELLES) hostInstitution 2˙399˙999.50
2    UNIVERSITE LIBRE DE BRUXELLES

 Organization address address: Avenue Franklin Roosevelt 50
city: BRUXELLES
postcode: 1050

contact info
Titolo: Prof.
Nome: Christine
Cognome: Courillon
Email: send email
Telefono: +32 2 6506718
Fax: +32 2 6502321

BE (BRUXELLES) hostInstitution 2˙399˙999.50

Mappa


 Word cloud

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epidermis    mechanisms    fate    repair    recently    cells    scs    postnatal    prostate    tracing    expansion    homeostasis    adult    cellular    clonal    modeling    gland    mammary    dynamics    lineage    tissue    mathematical    molecular    hierarchy    regeneration    proliferation   

 Obiettivo del progetto (Objective)

'Stem cells (SCs) ensure the development of the different tissues during morphogenesis, their physiological turnover during adult life and tissue repair after injuries. .

Our lab has recently developed new methods to study by lineage tracing the cellular hierarchy that sustains homeostasis and repair of the epidermis and to identify distinct populations of SCs and progenitors ensuring mammary gland and prostate postnatal development.

While quantitative clonal analysis combined with mathematical modeling has been used recently to decipher the cellular basis of tissue homeostasis, such experimental approaches have never been used so far in mammals to investigate the cellular hierarchy acting during tissue expansion such as postnatal development and tissue repair.

In this project, we will use a multi-disciplinary approach combining mouse genetic lineage tracing and clonal analysis, mathematical modeling, proliferation kinetics, transcriptional profiling, and functional experiments to investigate the cellular and molecular mechanisms regulating tissue expansion during epithelial development and tissue repair and how the fate of these cells is controlled during this process.

1. We will define the clonal and proliferation dynamics of tissue expansion in the epidermis, the mammary gland and the prostate during postnatal growth and adult tissue regeneration. 2. We will define the clonal and proliferation dynamics of tissue expansion in the adult epidermis following wounding and mechanical force mediated tissue expansion. 3. We will define the mechanisms that regulate the switch from multipotent to unipotent cell fate during development of glandular epithelia.

Defining the cellular and molecular mechanisms underlying tissue growth and expansion during development and how these mechanisms differ from tissue regeneration in adult may have important implications for understanding the causes of certain developmental defects and for regenerative medicine.'

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