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Grant: Operating Grant

Université de Montréal

$816,820.00

Restoring In Vivo Glial Functions At Neuromuscular Junctions: A New Therapeutic Target In ALS

EF 2014-15

Résumé
The communication between nerve cells and muscles is impaired in ALS and the neuromuscular synapses, nerve contacts that control muscle activity, are destroyed. The destruction of the neuromuscular synapse causes the disconnection between the nervous system and the muscles, leading to paralysis. In addition to nerve cells, the other main cell type in the nervous system are glial cells. These cells are also affected in ALS. Our current work will examine the contribution of specialized glial cells at the neuromuscular synapse. They ensure the stability of the neuromuscular synapse and participate in its repair should injury arise. This proposed research aims at restoring the properties of these glial cells so as to restore their normal function. The approach aims at preventing the destruction of the neuromuscular synapse, thus maintaining a better control of muscles by the nervous system. This work would also unravel novel avenues to understand the causes of ALS and lead to possible clinical applications.
Programme
Operating Grant
Emplacement
Quebec, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
321956
Name
Robitaille Richard
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Neurosciences, Mental Health and Addiction
Theme2
Biomedical
Prcname2
Systems & Circuits Neurosciences - A
Projecttitle
Restoring In Vivo Glial Functions At Neuromuscular Junctions: A New Therapeutic Target In ALS
Programtype2
Operating Grants
Orgnameinp2
Université de Montréal
Cihramount2
$816,820
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Aging; Als; Neuromuscular Junction; Neuron-Glia Interactions; Perisynaptic Schwann Cells; Synapses; Synaptic Plasticity
Abstract
The communication between nerve cells and muscles is impaired in ALS and the neuromuscular synapses, nerve contacts that control muscle activity, are destroyed. The destruction of the neuromuscular synapse causes the disconnection between the nervous system and the muscles, leading to paralysis. In addition to nerve cells, the other main cell type in the nervous system are glial cells. These cells are also affected in ALS. Our current work will examine the contribution of specialized glial cells at the neuromuscular synapse. They ensure the stability of the neuromuscular synapse and participate in its repair should injury arise. This proposed research aims at restoring the properties of these glial cells so as to restore their normal function. The approach aims at preventing the destruction of the neuromuscular synapse, thus maintaining a better control of muscles by the nervous system. This work would also unravel novel avenues to understand the causes of ALS and lead to possible clinical applications.
Competitiondate
201503
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Robitaille, Richard
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $816,820~ $0~