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PathAutoBIO SIGNED

Uncovering the pathway of DNA-induced autophagy and its biological functions in viral central nervous system infection

Total Cost €

0

EC-Contrib. €

0

Partnership

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 PathAutoBIO project word cloud

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

integrate    acids    persist    recycling    degradative    central    function    threats    plays    models    explore    roles    insights    immunity    infection    induction    defense    cancers    regulations    infectious    inflammation    deep    cell    likewise    background    expertise    cytometry    vivo    poses    collaborators    editing    host    balance    autophagy    stem    site    molecule    regulating    global    dna    advantage    varied    subsequent    infect    nucleic    tools    difficulties    innovative    imagestream    fighting    combine    metabolic    harmful    pathautobio    cells    societies    unknown    regulation    autoimmune    cross    activation    spectrum    mechanisms    lab    biology    showed    therapies    sting    pathogens    genome    hosts    vitro    cutting    sensing    links    brain    pivotal    coordinate    viral    neurodegeneration    pathogen    strategies    flow    decipher    broad    clearance    human    leads    presenting    mediated    themselves    immune    combined    international    diseases    functions    nervous    infections    protective    elusive    crispr    adaptor    cytosolic    edge    cas9   

Project "PathAutoBIO" data sheet

The following table provides information about the project.

Coordinator
AARHUS UNIVERSITET 

Organization address
address: NORDRE RINGGADE 1
city: AARHUS C
postcode: 8000
website: www.au.dk

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 Denmark [DK]
 Total cost 200˙194 €
 EC max contribution 200˙194 € (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 2018
 Duration (year-month-day) from 2018-05-01   to  2020-04-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    AARHUS UNIVERSITET DK (AARHUS C) coordinator 200˙194.00

Map

 Project objective

Pathogens establish a range of strategies to efficiently infect and persist in their hosts. These mechanisms are as varied as pathogens themselves, which poses many difficulties for fighting infections. A deep understanding of host defense mechanisms is thus crucial for developing innovative therapies. Sensing of pathogen-derived nucleic acids is pivotal for induction of host defense. The adaptor molecule STING plays a central role in this defense and coordinate activation of immune responses. Recent studies showed that cytosolic DNA sensing and subsequent STING activation also leads to induction of autophagy, a degradative pathway involved in metabolic recycling and regulation of infections and immunity. Both STING and autophagy are involved in a range of diseases e.g. infectious and autoimmune diseases, neurodegeneration and cancers. However, the links between STING and autophagy and their regulation of the balance between protective responses and harmful inflammation is elusive. Likewise, the roles of STING-mediated autophagy during viral infections is unknown. Using cutting-edge tools e.g. ImageStream X flow cytometry and genome-editing of human stem cells-derived brain cells using CRISPR/Cas9, PathAutoBIO will decipher the pathway of this novel STING function. We will then combine in vitro and in vivo models of central nervous system viral infection to explore STING-mediated autophagy functions at this unique site, where autophagy and STING are important for viral clearance. We will build upon the expertise of the host lab in DNA sensing, take advantage of unique tools developed for the project, and integrate leading international collaborators. Combined with my strong background in infection cell biology, our work will provide insights on the cross-regulations between autophagy and immunity. This will lead to a broader understanding of mechanisms regulating diseases presenting global threats for societies and will help the design of broad-spectrum therapies.

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

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