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PREMNEC SIGNED

PReterm Enteroids to determine the Mechanism of Necrotising EnteroColitis

Total Cost €

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EC-Contrib. €

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Partnership

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 PREMNEC project word cloud

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

phie    pathology    gut    causes    24    phies    pathobiology    cells    divided    week    wp1    translating    yielded    accurate    interaction    transcriptomics    fresh    crosstalk    packages    potentially    human    tissue    enteroids    inflammatory    wps    lack    functioning    invasive    undergo    utilising    systematically    preterm    infants    inability    poorly    culture    premnec    discarded    treatment    isolated    surgically    permit    stool    cellular    bowel    microbial    longstanding    otherwise    progress    newcastle    reproducible    colonisation    vivo    vixo    proteomics    characterisation    mechanisms    completion    mediated    wp    ex    hurdle    added    first    protection    expertise    mechanistic    co    imaging    beneficial    species    relates    concurrently    intestinal    single    extremely    explore    enteroid    pathogenesis    life    crypt    enterocolitis    robustly    abnormal    overcome    model    nec    host    microbiome    bacterial    few    university    samples    fellowship    prematurity    necrotising    bacteria    utilised    risk    deaths    resected    isolate    utilise    metagenomics    pioneered    technologies    regarded    disease   

Project "PREMNEC" data sheet

The following table provides information about the project.

Coordinator
UNIVERSITY OF NEWCASTLE UPON TYNE 

Organization address
address: KINGS GATE
city: NEWCASTLE UPON TYNE
postcode: NE1 7RU
website: http://www.ncl.ac.uk/

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 United Kingdom [UK]
 Total cost 183˙454 €
 EC max contribution 183˙454 € (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 2018-07-01   to  2020-06-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    UNIVERSITY OF NEWCASTLE UPON TYNE UK (NEWCASTLE UPON TYNE) coordinator 183˙454.00

Map

 Project objective

Necrotising enterocolitis (NEC) is an inflammatory mediated bowel disease that causes more deaths after the first week of life in extremely preterm infants than any other single pathology, with prematurity and abnormal bacterial colonisation regarded as the most significant risk factors. However, 40 years of research have yielded few advances in treatment and the mechanisms of disease remain poorly understood. A major reason for this lack of progress relates to challenges in translating findings from non-invasive samples (e.g., stool) and the inability to robustly model bacterial-host crosstalk. To overcome this longstanding hurdle, the proposed PREMNEC (PReterm Enteroids to determine the Mechanisms of Necrotising EnteroColitis) fellowship will utilise a novel ex vivo preterm human intestinal enteroid (PHIE) co-culture model to systematically explore the gut microbiome and host functioning in preterm infants. The fellowship is divided in three distinct work packages (WPs). In WP1, surgically resected intestinal tissue (otherwise discarded) from NEC and non-NEC infants will undergo characterisation utilising metagenomics, transcriptomics, proteomics, and cellular imaging directly on the fresh tissue. Concurrently, WP 2 will isolate crypt cells from the tissue to establish PHIEs that permit accurate and reproducible ex vixo co-culture of bacterial-host interaction. In WP 3, bacterial species isolated from preterm infants will be systematically added to the ex vixo co-culture model and comparable technologies utilised in WP 1 will be applied to determine the pathobiology of disease. Newcastle University will provide expertise in state-of-the-art transcriptomics and cellular imaging technologies. Upon completion of this 24-month fellowship, I will have pioneered significant advancement in the mechanistic understanding of microbial-host interaction in the pathogenesis of NEC and identified potentially beneficial bacteria that may provide protection from NEC.

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