LIFE-HIS-T

Mapping the life histories of T cells

 Coordinatore STICHTING HET NEDERLANDS KANKER INSTITUUT 

Spiacenti, non ci sono informazioni su questo coordinatore. Contattare Fabio per maggiori infomrazioni, grazie.

 Nazionalità Coordinatore Netherlands [NL]
 Totale costo 2˙499˙640 €
 EC contributo 2˙499˙640 €
 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-2010-AdG_20100317
 Funding Scheme ERC-AG
 Anno di inizio 2011
 Periodo (anno-mese-giorno) 2011-05-01   -   2016-04-30

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    STICHTING HET NEDERLANDS KANKER INSTITUUT

 Organization address address: PLESMANLAAN 121
city: AMSTERDAM
postcode: 1066 CX

contact info
Titolo: Dr.
Nome: Henri
Cognome: Van Luenen
Email: send email
Telefono: 31205122097

NL (AMSTERDAM) hostInstitution 2˙499˙640.00
2    STICHTING HET NEDERLANDS KANKER INSTITUUT

 Organization address address: PLESMANLAAN 121
city: AMSTERDAM
postcode: 1066 CX

contact info
Titolo: Prof.
Nome: Antonius Nicolaas Maria
Cognome: Schumacher
Email: send email
Telefono: 31205122072

NL (AMSTERDAM) hostInstitution 2˙499˙640.00

Mappa


 Word cloud

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

fate    antigen    individual    arise    progeny    determine    time    responses    memory    cells    cell   

 Obiettivo del progetto (Objective)

'T cells display many different phenotypes and functions, depending on the nature of previously encountered signals. If we want to understand how these different T cell subsets arise, we need to be able to follow individual T cells and their progeny through time. With the aim to map the life histories of individual T cells we have developed unique technologies that allow us to determine whether different T cell populations arise from common or distinct progenitors.

Within this project we will utilize genetic reporter systems to determine: 1. How T cell recruitment, proliferation and death shape antigen-specific T cell responses 2. At which stage the resulting T cells commit to the effector or the memory T cell lineage 3. The self renewal potential of the tissue-resident memory T cells that remain after infection is cleared

By following T cells and their progeny through time, this project will describe the regulation of cell fate in antigen-specific T cell responses. Furthermore, this project will lead to the creation of novel reporters of cellular history that will be of broad value to analyze cell fate and kinship for a variety of cell types.'

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