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INFLAME SIGNED

Deciphering the host and microbial grounds that license inflammasome-mediated execution

Total Cost €

0

EC-Contrib. €

0

Partnership

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 INFLAME project word cloud

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

vitro    cas9    protein    inflammasome    unsuspected    disorders    inducible    biology    ligands    sensors    canonical    combination    automated    parts    18    crispr    vivo    screening    interferon    technologies    immunity    paradigms    pathogens    coupling    unravel    proteins    bases    activation    play    components    auto    cytosolic    complexes    multidisciplinary    beta    infections    throughput    interleukin    induce    cytokines    host    detection    mediate    dependent    molecular    therapies    angles    innovative    directed    biochemistry    functions    caspase    intracellular    maturation       necrosis    visual    sensing    unbiased    expertise    breakthroughs    search    inflammasomes    infectious    diseases    forming    building    effectors    nucleate    pro    regulators    gasdermin    release    microbial    inflammatory    models    pyroptosis    cell    protease    unprecedented    immune    genome    entirely    regulated    il    gasdermins    proteases    unexplored    immunology   

Project "INFLAME" data sheet

The following table provides information about the project.

Coordinator
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE CNRS 

Organization address
address: RUE MICHEL ANGE 3
city: PARIS
postcode: 75794
website: www.cnrs.fr

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 France [FR]
 Total cost 1˙498˙799 €
 EC max contribution 1˙498˙799 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2018-STG
 Funding Scheme ERC-STG
 Starting year 2018
 Duration (year-month-day) from 2018-12-01   to  2023-11-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE CNRS FR (PARIS) coordinator 1˙498˙799.00

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 Project objective

Inflammasomes are intracellular multi-protein complexes that play essential functions in immunity against microbial pathogens. Upon microbial sensing, inflammasomes induce protease caspase-1-dependent maturation and release of the pro-inflammatory cytokines interleukin (IL)-1β and IL-18 as well as gasdermin-D-dependent cell necrosis, namely pyroptosis. While both pyroptosis and IL-1β/IL-18 release play key parts in controlling microbial infections, the host-regulated pathways that promote detection of microbial ligands by cytosolic inflammasome-forming sensors and the non-canonical functions of inflammasome-derived components, remain to be fully characterized.

Building on my expertise in the field of inflammasome regulators during microbial infections, I propose to study several key, yet unexplored aspects of the functions of inflammasomes in immunity from different angles. In particular, I propose to 1/ identify and characterize new host interferon-inducible factors that mediate microbial sensing by the inflammasomes, and 2/ unravel new non-canonical functions of inflammasome-derived proteases and gasdermins. To address these issues, I will use a combination of state-of-the-art and innovative technologies in biochemistry, molecular and cell biology, and immunology in various in vitro and in vivo models. For example, I propose to develop an unbiased genome-wide search for novel effectors involved in inflammasome activation based on the unprecedented coupling of the CRISPR-Cas9 technology to automated visual high-throughput screening.

This multidisciplinary proposal will provide breakthroughs in the field of microbial pathogens detection by the host immune system, and will nucleate entirely novel immune paradigms on microbial sensing by new unsuspected host cytosolic proteins, namely the gasdermins. The results of this project will also provide strong bases for building innovative host-directed therapies for auto-inflammatory disorders and infectious diseases.

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The information about "INFLAME" are provided by the European Opendata Portal: CORDIS opendata.

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