Grant: Operating Grant
McGill University
$829,373.00
Molecular Mechanisms of Growth Cone Collapse and Neurite Outgrowth Inhibition
EF 2013-14
Résumé
Neurons in the Central Nervous System (CNS) fail to regenerate because of molecules in the environment that block nerve cell repair. This fundamental problem is the basis for much of the clinical disability associated with spinal cord injury and stroke. By identifying the proteins involved in signalling to injured nerve cells to block nerve cell repair, one can develop strategies to overcome the inhibitory nature of the CNS environment. The aim of this grant is to test if we can enhance regeneration in an animal model of CNS injury by inhibiting CRMP4, a protein that we have shown blocks nerve cell repair in a cell culture model. We will also further study the molecular mechanisms through which CRMP4 affects nerve cell repair in an effort to identify additional molecules that may be therapeutic targets for promoting nerve regeneration.
Programme
Operating Grant
Bénéficiaire
Emplacement
Quebec, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
303775
Name
Fournier Alyson Elise
Region
Québec
Country
Canada
Orgtype
Research Institution; Institution Paid
Instname2
Neurosciences, Mental Health and Addiction
Theme2
Biomedical
Prcname2
Molecular & Cellular Neurosciences - B
Projecttitle
Molecular Mechanisms of Growth Cone Collapse and Neurite Outgrowth Inhibition
Programtype2
Operating Grants
Orgnameinp2
McGill University
Cihramount2
$829,373
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Axon Growth; Crmp; Cytoskeletal Dynamics; Regeneration
Abstract
Neurons in the Central Nervous System (CNS) fail to regenerate because of molecules in the environment that block nerve cell repair. This fundamental problem is the basis for much of the clinical disability associated with spinal cord injury and stroke. By identifying the proteins involved in signalling to injured nerve cells to block nerve cell repair, one can develop strategies to overcome the inhibitory nature of the CNS environment. The aim of this grant is to test if we can enhance regeneration in an animal model of CNS injury by inhibiting CRMP4, a protein that we have shown blocks nerve cell repair in a cell culture model. We will also further study the molecular mechanisms through which CRMP4 affects nerve cell repair in an effort to identify additional molecules that may be therapeutic targets for promoting nerve regeneration.
Competitiondate
201403
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Fournier, Alyson Elise
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $829,373~ $0~