Opendata, web and dolomites

GCB-PRID SIGNED

Post-transcriptional Regulation of Germinal Center B Cell Responses in Immunity and Disease

Total Cost €

0

EC-Contrib. €

0

Partnership

0

Views

0

 GCB-PRID project word cloud

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

elucidate    disciplinary    networks    gc    biology    antibody    cell    physiology    proteomics    plasma    immune    functions    protein    pinpoint    reactions    mechanisms    immunity    profoundly    plasmacytic    molecular    significantly    proteins    rna    licensed    differ    mouse    viruses    power    sensors    biochemistry    mantle    regulation    complement    steadily    cytokines    conduct    thereby    exert    list    protective    immunology    prid    cellular    found    molecularly    abundance    hallmark    gcb    fluorescent    exercise    uncover    cells    pathogenic    unfortunately    mediators    germinal    transcriptional    barrier    expression    regulating    screens    critical    center    secreting    vaccinations    ultimately    little    regulatory    reveal    insights    adaptive    diseases    antibodies    post    binding    models    transcription    autoantibodies    proinflammatory    fates    promises    secreted    bacteria    incidence    culture    rbp    zone    rivals    differentiation    rbps    genetic    postulate    treatment    sophisticated    groundbreaking    autoimmune    monitor   

Project "GCB-PRID" data sheet

The following table provides information about the project.

Coordinator
KLINIKUM RECHTS DER ISAR DER TECHNISCHEN UNIVERSITAT MUNCHEN 

Organization address
address: ISMANINGER STRASSE 22
city: MUENCHEN
postcode: 81675
website: http://www.med.tu.muenchen.de

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 Germany [DE]
 Project website https://www.translatum.tum.de/research-groups/immunopathology-and-signal-transduction/
 Total cost 1˙998˙066 €
 EC max contribution 1˙998˙066 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2015-CoG
 Funding Scheme ERC-COG
 Starting year 2016
 Duration (year-month-day) from 2016-09-01   to  2022-08-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    KLINIKUM RECHTS DER ISAR DER TECHNISCHEN UNIVERSITAT MUNCHEN DE (MUENCHEN) coordinator 1˙998˙066.00

Map

 Project objective

Antibodies secreted by B cells of the adaptive immune system establish an essential barrier against bacteria and viruses and their presence is the hallmark of protective vaccinations. B cells are licensed for their tasks during germinal center (GC) reactions and differentiation into antibody-secreting plasma cells. Unfortunately, B cell-derived autoantibodies and proinflammatory cytokines can cause or contribute to autoimmune diseases.

While major transcription factor networks regulating protective (or pathogenic) GCB cell responses have been identified and characterized, little is known about the post-transcriptional regulation by RNA-binding proteins (RBP), whose number rivals that of transcription factors. We postulate that RBPs exercise critical post-transcriptional control over germinal center B (GCB) and plasmacytic cell physiology and we aim to identify and molecularly characterize these regulatory mechanisms.

To this end, we will complement sophisticated genetic mouse models with novel cell culture systems. We will monitor RBP activity with fluorescent sensors and use proteomics to reveal RBPs regulating the protein abundance of critical mediators of GCB and plasmacytic cell fates. In addition, we will conduct genetic screens to uncover relevant functions of a short list of 40 RBPs, whose protein expression we found to differ significantly between GCB and mantle zone B cells. Ultimately, we will use cellular immunology and RNA biochemistry to elucidate how these RBPs exert their post-transcriptional control.

Through the integrated power of our multi-disciplinary approach we will thus pinpoint and investigate the functions of key RBPs regulating the biology of GCB and plasmacytic cells. GCB-PRID promises to uncover profoundly new insights into post-transcriptional regulation of adaptive immunity. Thereby, this groundbreaking research aims to reveal novel molecular targets for the treatment of autoimmune diseases, whose incidence is steadily on the rise.

 Publications

year authors and title journal last update
List of publications.
2019 Maike Kober-Hasslacher, Marc Schmidt-Supprian
The Unsolved Puzzle of c-Rel in B Cell Lymphoma
published pages: 941, ISSN: 2072-6694, DOI: 10.3390/cancers11070941
Cancers 11/7 2020-01-20

Are you the coordinator (or a participant) of this project? Plaese send me more information about the "GCB-PRID" 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 "GCB-PRID" are provided by the European Opendata Portal: CORDIS opendata.

More projects from the same programme (H2020-EU.1.1.)

CohoSing (2019)

Cohomology and Singularities

Read More  

ERC VP CSA (2018)

Support to the Vice-Presidents of the ERC Scientific Council 2018

Read More  

CURVE-X (2019)

Industrialisation of curved sensors and related imagers

Read More