INVIVO TCELL IMAGING

Twophoton microscopy analysis of phosphoinositide-3 kinase function during primary and secondary T cell activation in vivo

 Coordinatore UNIVERSITAET BERN 

 Organization address address: Hochschulstrasse 4
city: BERN
postcode: 3012

contact info
Titolo: Ms.
Nome: Marianne
Cognome: Schori
Email: send email
Telefono: +41 31 6314141

 Nazionalità Coordinatore Switzerland [CH]
 Totale costo 179˙101 €
 EC contributo 179˙101 €
 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-2010-IIF
 Funding Scheme MC-IIF
 Anno di inizio 2011
 Periodo (anno-mese-giorno) 2011-04-01   -   2013-03-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    UNIVERSITAET BERN

 Organization address address: Hochschulstrasse 4
city: BERN
postcode: 3012

contact info
Titolo: Ms.
Nome: Marianne
Cognome: Schori
Email: send email
Telefono: +41 31 6314141

CH (BERN) coordinator 179˙101.60

Mappa


 Word cloud

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

initiation    effector    molecules    cd    interactions    vivo    perform    pm    pln    cell    cells    adaptive    dc    immune    dynamic    model    flow    pmhc    antigen    activation    imaging    secondary    mutant    inside       delta    pi    primary   

 Obiettivo del progetto (Objective)

'The adaptive immune system protects us from nocuous microbes, yet excessive immune reactions can lead to the development of autoimmunity. The initiation of adaptive immune responses takes place in lymphoid organs, including peripheral lymph nodes (PLN). Inside PLN, T cells become activated through the molecular interactions of the T cell receptor with cognate peptide-MHC (pMHC) molecules and costimulatory molecules on dendritic cells (DC). TCR-mediated signals lead to the activation of the phosphoinositol-3-kinase (PI3K) pathway via the PI3Kδ isoform, which is required for full T cell activation in vitro. However, little is known about the role of the PI3Kδ during primary and secondary in vivo T cell activation. Here, we will use twophoton microscopy (2PM) to observe the interactions of antigen-specific control and PI3Kδ-mutant CD4 T cells and pMHC-loaded DC deep inside PLN of live, anesthetized mice. Comparing the dynamic interaction parameters obtained in 2PM imaging with the flow cytometric analysis of the activation status of control and PI3Kδ-mutant T cells, we will delineate the precise contribution of the PI3Kδ for primary T cell activation in vivo. We will furthermore perform an analysis of the secondary activation of control and PI3Kδ-mutant effector CD4 T cells in a mouse model of antigen-induced arthritis. Therefore, we will establish an intravital knee-joint 2PM model to follow the dynamic behavior of control and PI3Kδ-mutant effector T cells with antigen-presenting macrophages in the inflamed tissue. We will combine imaging data with disease scoring, flow cytometry and the use of a PI3Kδ-specific pharmacological inhibitor for a comprehensive analysis of PI3Kδ function at sites of inflammation. In summary, we propose to perform an in-depth analysis of the role of PI3Kδ during adaptive immune response initiation and maintenance. This is also clinically relevant since PI3Kδ inhibitors are in development for immunomodulation.'

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