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.

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

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.)

NSTree (2020)

Understanding substrate delivery for cell wall biosynthesis in plants

Read More  

EngPTC2 (2019)

Exploring new technologies for the next generation pulse tube cryocooler below 2K

Read More  

MemoryAggregates (2020)

Mechanism of Whi3 Aggregation and its Age-dependent Malfunction

Read More