Opendata, web and dolomites

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

0

Views

0

 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.

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

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.

Are you the coordinator (or a participant) of this project? Plaese send me more information about the "PATHAUTOBIO" project.

For instance: the website url (it has not provided by EU-opendata yet), the logo, a more detailed description of the project (in plain text as a rtf file or a word file), some pictures (as picture files, not embedded into any word file), twitter account, linkedin page, etc.

Send me an  email (fabio@fabiodisconzi.com) and I put them in your project's page as son as possible.

Thanks. And then put a link of this page into your project's website.

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

More projects from the same programme (H2020-EU.1.3.2.)

MarshFlux (2020)

The effect of future global climate and land-use change on greenhouse gas fluxes and microbial processes in salt marshes

Read More  

HSQG (2020)

Higher Spin Quantum Gravity: Lagrangian Formulations for Higher Spin Gravity and Their Applications

Read More  

DIFFER (2020)

Determinants of genetic diversity: Important Factors For Ecosystem Resilience

Read More