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.

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

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.)

5G-ACE (2019)

Beyond 5G: 3D Network Modelling for THz-based Ultra-Fast Small Cells

Read More  

MemoryAggregates (2020)

Mechanism of Whi3 Aggregation and its Age-dependent Malfunction

Read More  

SAInTHz (2020)

Structuration of aqueous interfaces by Terahertz pulses: A study by Second Harmonic and Sum Frequency Generation

Read More