Canada Spends Logo

Explorez notre analyse du budget 2026

Grant: Project Grant

University of Calgary

$1,032,750.00

Pannexin-1 Opening in Neurons: Mechanisms of Intrinsic Neuroprotection

EF 2019-20

Résumé
Stroke is a leading cause of disability and death in Canada. When the blood supply to the brain is disrupted, either regionally or globally, the nerve cells can rapidly malfunction and die. Neuronal death during stroke has several characteristic features, including loss of the cell's electrical activity and the formation of blebs in their processes (dendrites). Interestingly, nerve cells that reside outside the core of the stroke damage show blebbing in their dendritic regions that cross into the core, but may ultimately survive the insult. Here we propose that the molecular machinery responsible for bleb formation functions in a protective role. This is achieved by isolation of damaging signals (calcium) from spreading to the rest of the cell. We propose that by understanding how these traditionally damaging structures (blebs) form and potentially protect the nerve cells will form a basis for exploiting them in the future to reduce brain damage and improve recovery after stroke.
Programme
Project Grant
Bénéficiaire
Emplacement
Alberta, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
408350
Name
Thompson Roger J
Region
Alberta
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Neurosciences, Mental Health and Addiction
Theme2
Biomedical
Prcname2
Molecular & Cellular Neurosciences - B
Projecttitle
Pannexin-1 Opening in Neurons: Mechanisms of Intrinsic Neuroprotection
Programtype2
Operating Grants
Orgnameinp2
University of Calgary
Cihramount2
$1,032,750
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
2 Photon Imaging; Excitotoxicity; Metabrotropic Nmda Receptor; Molecular Biology; Nmda Receptor; Pannexin-1; Patch-Clamp; Src Kinase; Stroke
Abstract
Stroke is a leading cause of disability and death in Canada. When the blood supply to the brain is disrupted, either regionally or globally, the nerve cells can rapidly malfunction and die. Neuronal death during stroke has several characteristic features, including loss of the cell's electrical activity and the formation of blebs in their processes (dendrites). Interestingly, nerve cells that reside outside the core of the stroke damage show blebbing in their dendritic regions that cross into the core, but may ultimately survive the insult. Here we propose that the molecular machinery responsible for bleb formation functions in a protective role. This is achieved by isolation of damaging signals (calcium) from spreading to the rest of the cell. We propose that by understanding how these traditionally damaging structures (blebs) form and potentially protect the nerve cells will form a basis for exploiting them in the future to reduce brain damage and improve recovery after stroke.
Competitiondate
201909
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Thompson, Roger J
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $1,032,750~ $0~