S.CE.N.E.

Deconstructing the stem cell niche in human interfollicular epidermis in vitro

 Coordinatore KING'S COLLEGE LONDON 

 Organization address address: Strand
city: LONDON
postcode: WC2R 2LS

contact info
Titolo: Mr.
Nome: Paul
Cognome: Labbett
Email: send email
Telefono: 442078000000

 Nazionalità Coordinatore United Kingdom [UK]
 Totale costo 221˙606 €
 EC contributo 221˙606 €
 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-2012-IEF
 Funding Scheme MC-IEF
 Anno di inizio 2013
 Periodo (anno-mese-giorno) 2013-03-01   -   2015-02-28

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    KING'S COLLEGE LONDON

 Organization address address: Strand
city: LONDON
postcode: WC2R 2LS

contact info
Titolo: Mr.
Nome: Paul
Cognome: Labbett
Email: send email
Telefono: 442078000000

UK (LONDON) coordinator 221˙606.40

Mappa


 Word cloud

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

fate    adhesion    responses    stem    cells    receptors    signals    extrinsic    intercellular    epidermal    adult    own    significantly    niche    cell    biology    substrate    intrinsic   

 Obiettivo del progetto (Objective)

'Within adult tissues, stem cell properties are heavily influenced by their microenvironment, or niche. In the niche, stem cells integrate a complex array of extrinsic molecular signals that, in concert with cell-intrinsic regulatory networks, control self-renewal and differentiation in response to physiologic demands. By studying adult human epidermal stem cells ex vivo using artificial microenvironments (micro-patterned adhesive islands and hydrogels of differing bulk stiffness) we will investigate two questions: (1) What is the importance of intercellular adhesion in regulating epidermal stem cell fate? (2) How does the genetic state of a stem cell affect its responses to extrinsic signals? Combining state-of-the-art methodologies in biomaterials science and cell biology we will address whether cell-cell and cell-substrate signals have synergistic or antagonist effects on stem cell fate decisions, and whether one type of signal can over-ride another. Specific cell adhesion receptors will be engaged by recombinant proteins bound to latex beads, while specific cell-cell contacts will be engineered via avidin-biotin interaction. We will also investigate how intrinsic modulation of the Notch and Wnt signaling pathways changes epidermal stem cell responses to different niche signals of substrate contact area, substrate porosity and the engagement of specific intercellular adhesion receptors. The proposed project will be carried out at the Centre for Stem Cells & Regenerative Medicine, one of Europe's newest hot spots for stem cell research, based at King's College London, with Prof. Fiona Watt, a world expert in somatic stem cells, as scientist in charge. In such ideal surroundings, the fellow will be able to stimulate and advance European stem cell research, to significantly strengthen his own expertise in skin biology and to add novel research competences, and to establish his own network of collaborations in order to significantly advance his career development.'

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