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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.

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

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

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 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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