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LinkFM SIGNED

Linking Functional impact and Microstructural properties of fiber tract demyelination and remyelination in a rodent model of multiple sclerosis

Total Cost €

0

EC-Contrib. €

0

Partnership

0

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 LinkFM project word cloud

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

cell    intracellular    wrapped    propagation    myelinisation    sheaths    recording    reparatory    microstructural    myelination    mr    circuits    drcmr    trace    lesioned    quantitative    expertise    multiple    integrates    resting    network    disease    de    optogenetics    impairing    calcium    integration    biomarkers    functional    poorly    axons    parallel    diameter    combine    neurodegenerative    connectivity    diffusion    cortical    inter    nervous    exact    degeneration    simultaneous    sclerosis    content    relationship    axonal    repair    mapping    monitoring    trans    myelin    model    treatment    optimize    lines    inflammatory    prospectively    connected    ms    patients    central    destroys    white    re    biophysical    sequences    delays    neuronal    personalized    damage    amount    neuroinflammation    demyelination    brain    optimized    dysfunction    sensitive    leads    dynamics    cellular    blocks    voltage    trigger    scales    axon    models    signal    rat    membrane    create    multimodal    perform    informing    yield    primary    ing    bridge    disentangle    remyelination    leveraging    building    diffuse    tract    framework    temporal    tracts    mri   

Project "LinkFM" data sheet

The following table provides information about the project.

Coordinator
REGION HOVEDSTADEN 

Organization address
address: KONGENS VAENGE 2
city: HILLEROD
postcode: 3400
website: www.regionh.dk

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 Denmark [DK]
 Total cost 219˙312 €
 EC max contribution 219˙312 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2018
 Funding Scheme MSCA-IF-EF-SE
 Starting year 2019
 Duration (year-month-day) from 2019-05-01   to  2021-04-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    REGION HOVEDSTADEN DK (HILLEROD) coordinator 219˙312.00

Map

 Project objective

Multiple sclerosis (MS) is a diffuse inflammatory and neurodegenerative disease of the central nervous system. Neuroinflammation destroys the myelin sheaths wrapped around the axons and may lead to axon degeneration. Repair processes trigger re-myelinisation. Myelin loss delays or blocks signal propagation along axons in white matter tracts, impairing neuronal integration within the affected brain network. The exact relationship between the amount of axonal de- and re-myelination and the resulting network dysfunction is still poorly understood. Using a rat MS model, I will bridge the scales from the cellular to the network level, to disentangle how myelin loss and axonal degeneration leads to network dysfunction. My approach integrates three lines of research: (i) I will prospectively perform diffusion MRI and quantitative MRI to assess the temporal dynamics of microstructural changes in axon diameter and myelin content in the lesioned white matter tract. Leveraging state-of-art expertise at DRCMR, I will optimize MR sequences and biophysical models to create an optimized axon diameter and myelin mapping framework. (ii) In parallel, I will perform resting-state and task-based functional MRI to trace the resulting changes in functional connectivity at the network level. (iii) Building on my expertise, I will combine functional MRI with optogenetics and simultaneous intracellular calcium (and trans-membrane voltage) recording to characterize in detail the functional impact of axonal damage in the lesioned white matter tract on well-defined cell circuits in the inter-connected cortical areas. This unique multimodal approach will yield novel MRI-based biomarkers that are sensitive and specific to primary demyelination and axonal degeneration on the one hand and reparatory processes such as remyelination on the other hand. These biomarkers will have great potential for monitoring disease activity, informing personalized treatment in patients with MS.

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

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