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NEMoCuRe SIGNED

Role of S-Nitrosylation of epigenetic modifiers in vascular regeneration

Total Cost €

0

EC-Contrib. €

0

Partnership

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 NEMoCuRe project word cloud

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

extensive    msca    nitrosylation    injury    site    dr    cardiovascular    data    mutagenesis    consist    decipher    plan    mentorship    tissues    zebrafish    epigenetic    foundations    lay    martin    supportive    trigger    nuclear    reader    denvir    regeneration    background    modulate    morpholinos    independent    transition    mentor    career    structured    danio    spec    provocative    matrone    situ    knocked    tissue    activation    pharmacologically    advantage    modifiers    lines    prepare    talented    strategies    rerio    vascular    proteins    confirm    cardiology    extracts    builds    interesting    tlr3    sciences    insights    track    preliminary    centre    disease    skills    biologist    excellent    laser    he    candidate    describes    mutated    injured    mass    crispr    nfkb    showing    transgenic    investigator    formal    coursework    edinburgh    proteomic    dorsal    humans    toward    aorta    mechanisms    innate    refine    immune    cas9    inos    university    genetically   

Project "NEMoCuRe" data sheet

The following table provides information about the project.

Coordinator
THE UNIVERSITY OF EDINBURGH 

Organization address
address: OLD COLLEGE, SOUTH BRIDGE
city: EDINBURGH
postcode: EH8 9YL
website: www.ed.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 195˙454 €
 EC max contribution 195˙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 2018-09-01   to  2020-08-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    THE UNIVERSITY OF EDINBURGH UK (EDINBURGH) coordinator 195˙454.00

Map

 Project objective

This MSCA-IF describes a career development plan to prepare Dr. Matrone to become an independent investigator. This program builds on Dr. Matrone’s background as a talented biologist in cardiovascular regeneration and will provide him with the skills to decipher the mechanisms of S-Nitrosylation of epigenetic modifiers during tissue regeneration in zebrafish (Danio rerio). These studies will lay the foundations for future studies that will be carried out by Dr. Matrone as an independent investigator. The project will be carried out at the Centre for Cardiovascular Sciences at the University of Edinburgh. Dr. Matrone’s mentor is Dr. Martin Denvir, Reader in Cardiology. Dr. Denvir is an excellent mentor with extensive experience in cardiovascular disease. The MSCA-IF will consist of structured mentorship, formal coursework, a provocative research project and a program of career transition. Dr. Matrone’s research proposal is based on supportive preliminary data. Changes in S-nitrosylation of epigenetic modifiers in response to injury will be assessed in nuclear proteins extracts from injured tissues and identified by mass spec-proteomic analyses. The most interesting and novel epigenetic modifiers will be further studied in vascular development and regeneration following laser injury in the dorsal aorta. Candidate proteins will be knocked out by CRISPR/Cas9 or knocked down by morpholinos and will be mutated by site-specific mutagenesis. Furthermore, Dr. Matrone will assess the role of the innate immune system and iNOS in S-nitrosylation of nuclear proteins (e.g. epigenetic modifiers). He will confirm and refine his preliminary data showing that the innate immune system and iNOS trigger tissue regeneration. He will pharmacologically and genetically modulate TLR3, NFkB and iNOS and will take advantage of transgenic lines to track changes in the immune system activation in situ. These studies may provide insights toward novel strategies for tissue regeneration in humans.

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