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COR1-TCELL SIGNED

Analysis of the role for coronin 1-dependent cell density signalling in T-cell homeostasis

Total Cost €

0

EC-Contrib. €

0

Partnership

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 COR1-TCELL project word cloud

Explore the words cloud of the COR1-TCELL project. It provides you a very rough idea of what is the project "COR1-TCELL" about.

career    adoptive    cells    molecular    antigen    lymphopenic    receptors    mechanisms    requirement    inducible    recognising    reconstituted    spectrometry    single    self    mass    environment    underlying    anti    immunotherapy    cutting    vitro    peripheral    originally    ad    regulated    newly    prevention    cell    harnessing    biology    unknown    mouse    co    autoimmune    elucidate    suggest    culture    hoc    preliminary    post    uncharacterized    immunity    interleukin    disorders    potentiate    transfer    homeostasis    repeat    expansion    family    rna    wd    experiments    survival    cancer    reveal    recapitulates    mediated    neonatal    lymphoid    contributes    stimulating    stage    molecules    loaded    knockout    coronin    technologies    newborns    assay    mechanism    cytokine    peptides    edge    protein    microbial    found    depends    sequencing    ablation    organs    explore    vivo    sensing    successful    hitherto    histocompatibility    density    utilising    biochemical    dependent    signalling    maintenance    delineate    combine    fellowship    presenting   

Project "COR1-TCELL" data sheet

The following table provides information about the project.

Coordinator
UNIVERSITAT BASEL 

Organization address
address: PETERSPLATZ 1
city: BASEL
postcode: 4051
website: www.unibas.ch

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country Switzerland [CH]
 Total cost 175˙419 €
 EC max contribution 175˙419 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2017
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2019
 Duration (year-month-day) from 2019-01-01   to  2020-12-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    UNIVERSITAT BASEL CH (BASEL) coordinator 175˙419.00

Map

 Project objective

Harnessing T-cell homeostasis is important for cancer immunotherapy as well as anti-microbial immunity and the prevention of autoimmune disorders. T-cell homeostasis in peripheral lymphoid organs is known to be regulated through interleukin-7-mediated cytokine signalling and via T-cell receptors recognising self-peptides loaded on major histocompatibility complex. However, recent results suggest a requirement of a third pathway at low T-cell density such as in newborns that depends on the WD repeat protein family member coronin 1, the mechanism of which is unknown. The objective of this proposal is to elucidate the molecular mechanism of coronin 1-dependent sensing of low cell density that contributes to peripheral T-cell homeostasis. In preliminary work, I established a co-culture assay of T cells and antigen presenting cells that recapitulates coronin 1-dependent T-cell survival at low cell density. In addition, I found that adoptive transfer experiments reconstituted the coronin 1-dependent peripheral T-cell expansion in a lymphopenic environment in vivo. To delineate the molecular mechanisms underlying this cell density-dependent signalling mediated by coronin 1, I will combine the originally established in vitro and in vivo assay systems with state-of-the-art single-cell RNA sequencing, in addition to biochemical analysis utilising mass spectrometry. This will identify the signalling pathways and the molecules involved in this density-sensing mechanism. Finally, ad-hoc ablation of coronin 1 using a newly established inducible knockout mouse will reveal the role for coronin 1 in the maintenance of peripheral T cells after successful expansion at post-neonatal stage. The results from this project will define a hitherto uncharacterized density-sensing pathway required for T-cell homeostasis. Furthermore, the fellowship will potentiate my career opportunities as it allows to explore cutting-edge biology and technologies in a highly stimulating research environment.

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The information about "COR1-TCELL" are provided by the European Opendata Portal: CORDIS opendata.

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