Grant: Operating Grant - JPND Cross-Disease Analysis of Pathways
University of Ottawa
$499,998.00
Cellular Bioenergetics in Neurodegenerative Diseases: A system-based pathway and target analysis.
EF 2014-15
Résumé
Increasing evidence suggests that mitochondria, a part of the cell which generates energy, are damaged in neurodegenerative diseases including PD and AD. How this dysfunction contributes to brain cell loss is unclear. Our current proposal will determine common mechanisms by which mitochondrial stress leads to brain cell loss. We will also develop pathways by which we can potentially reverse these deficits to block the degenerative process. To do this, we will use a variety of culture and animal models in mice, fly, and worms which reflect neurodegenerative conditions such as PD, AD, and HD. We will also utilize computational modeling to better predict the mitochondrial signals required for degeneration.
Programme
Operating Grant - JPND Cross-Disease Analysis of Pathways
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
314192
Name
Park David S
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Partnername
Royal College of Surgeons in Ireland (UK); Federal Ministry of Education and Research (Germany); Ministero della Salute (Italy); Swedish Research Council (Sweden)
Instname2
Neurosciences, Mental Health and Addiction
Theme2
Health systems / services
Prcname2
Special Cases
Projecttitle
Cellular Bioenergetics in Neurodegenerative Diseases: A system-based pathway and target analysis.
Programtype2
Operating Grants
Orgnameinp2
University of Ottawa
Cihramount2
$499,998
Cihrequipment2
$0
Programname2
Operating Grant - JPND Cross-Disease Analysis of Pathways
Keyworddelim
Bioenergetics; C. Elegans; Computational Modelling; D. Melanogaster; Disease Mechanisms; Hight-Throughput Drug Screen; Mitochondria; Second-Hit Hypothesis; Therapeutics; Transgenic Mouse Models
Abstract
Increasing evidence suggests that mitochondria, a part of the cell which generates energy, are damaged in neurodegenerative diseases including PD and AD. How this dysfunction contributes to brain cell loss is unclear. Our current proposal will determine common mechanisms by which mitochondrial stress leads to brain cell loss. We will also develop pathways by which we can potentially reverse these deficits to block the degenerative process. To do this, we will use a variety of culture and animal models in mice, fly, and worms which reflect neurodegenerative conditions such as PD, AD, and HD. We will also utilize computational modeling to better predict the mitochondrial signals required for degeneration.
Competitiondate
201406
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Park, David S
Approvedterm
3 ans 0 mois
Cihrcontribution2
Inst of Neurosc Mental Hlth &A~ $277,777~ $0~Institute of Aging~ $222,221~ $0~