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SCOPE SIGNED

Schwann Cell Options for chronic Pain Eradication

Total Cost €

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EC-Contrib. €

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Partnership

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 SCOPE project word cloud

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

message    paradigm    pain    nervous    inflamed    discovering    cell    neuroinflammation    identification    ensheath    peripheral    injured    channel    mouse    signalling    prototypical    stimuli    subpopulation    allodynia    model    channels    anticipate    combine    efficacy    analgesic    afflicts    trpa1    cells    unsatisfactory    observation    treatment    inflammatory    25    sustains    oligodendrocytes    rat    extend    autocrine    ankyrin    predictive    susceptibility    ligation    central    human    nociceptors    tissue    transducer    sciatic    fibres    nerve    adult    schwann    purpose    safety    entails    sensitivity    innocuous    sustain    primary    discovered    neuropathies    medical    medicines    lineages    population    mice    biosignatures    biomarkers    chronic    mild    eligible    repertoire    safer    amplification    inflammation    unknown    hitherto    acute    exerts    analgesics    neurons    neuropathic    paracrine    molecular    orchestrate    models    transient    enzymes    cancer    expressed    sensory    stress    oxidative    limited    brain    receptor   

Project "SCOPE" data sheet

The following table provides information about the project.

Coordinator
UNIVERSITA DEGLI STUDI DI FIRENZE 

Organization address
address: Piazza San Marco 4
city: Florence
postcode: 50121
website: http://www.unifi.it

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 Italy [IT]
 Total cost 2˙185˙921 €
 EC max contribution 2˙185˙921 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2018-ADG
 Funding Scheme ERC-ADG
 Starting year 2019
 Duration (year-month-day) from 2019-09-01   to  2024-08-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    UNIVERSITA DEGLI STUDI DI FIRENZE IT (Florence) coordinator 2˙185˙921.00

Map

 Project objective

Chronic pain, characterized by increased sensitivity to innocuous/mild stimuli (allodynia), afflicts 25% of the European adult population. Efficacy and/or safety of analgesic medicines is limited, and the treatment of chronic pain associated with inflammation, peripheral and central neuropathies and cancer remains unsatisfactory. Thus, identification of novel targets for better and safer analgesics is a major medical need. Transient receptor potential ankyrin 1 (TRPA1) channel, expressed by a subpopulation of primary sensory neurons (nociceptors), has been proposed as a major transducer of acute pain. We have, recently, identified that TRPA1 is expressed in Schwann cells that ensheath peripheral nerve fibres. In a prototypical model of neuropathic pain (sciatic nerve ligation in mice), we discovered that Schwann cell-TRPA1 exerts a hitherto unknown role that, via amplification of the oxidative stress message, sustains neuroinflammation and chronic pain (allodynia). Thus, Schwann cells, through their own repertoire of channels and enzymes orchestrate in the injured/inflamed tissue an autocrine/paracrine signalling pathway to sustain chronic pain. The purpose of the present project is to extend this observation to other models of inflammatory, neuropathic and cancer pain to identify a general paradigm based on Schwann cell/TRPA1/oxidative stress as the pathway that sustains chronic pain. We aim also at identifying in oligodendrocytes (the Schwann cells of the brain) whether the TRPA1/oxidative stress pathway sustains pain in the central nervous system. In mouse, rat and human Schwann cells/oligodendrocytes we aim at identifying biomarkers and combine them into biosignatures predictive of the susceptibility to the development of chronic pain. We anticipate that each molecular step that entails the TRPA1/oxidative stress pathway in Schwann cell lineages is an eligible target for discovering new effective and safer medicines for the treatment of chronic pain.

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The information about "SCOPE" are provided by the European Opendata Portal: CORDIS opendata.

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