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Grant: Foundation Grant

University of Ottawa

$2,682,655.00

Enhancing Mitochondrial Integrity to Promote Brain Regeneration and Repair

EF 2016-17

Résumé
It was always believed that the adult brains cannot regenerate damaged brain tissue and that brain cells (neurons) must last throughout life. Recently, it was found that the adult brain contains active stem cells and progenitor cells, which have the capacity to regenerate new neurons. A major challenge is that most neural stem cells lie dormant in the adult brain and their numbers decline with age. It is therefore essential to identify new strategies to activate and expand the adult stem cell population. Defects in mitochondria, the energy producing powerhouse of the cells, is associated with neurodegenerative diseases. The impact of mitochondrial impairment in adult stem and progenitor cells in the adult brain remains unknown. Our preliminary data shows that adult stem and progenitor cells are highly sensitive to changes in mitochondrial dynamics and loss of mitochondrial function causes a severe impairment in the development of new neurons in the adult brain. In these studies we will manipulate mitochondrial dynamics in an effort to prevent the decline of adult neurogenesis in the aging brain or in neurodegeneration. The overall goal is develop new treatment strategies by which to regenerate damaged brain tissue.
Programme
Foundation Grant
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
354831
Name
Slack Ruth S
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Neurosciences, Mental Health and Addiction
Theme2
Biomedical
Prcname2
Foundation Grant
Projecttitle
Enhancing Mitochondrial Integrity to Promote Brain Regeneration and Repair
Programtype2
Operating Grants
Orgnameinp2
University of Ottawa
Cihramount2
$2,682,655
Cihrequipment2
$0
Programname2
Foundation Grant
Keyworddelim
Aging; Mitochondria; Neural Stem Cell; Neurodegeneration; Neurogenesis; Stroke
Abstract
It was always believed that the adult brains cannot regenerate damaged brain tissue and that brain cells (neurons) must last throughout life. Recently, it was found that the adult brain contains active stem cells and progenitor cells, which have the capacity to regenerate new neurons. A major challenge is that most neural stem cells lie dormant in the adult brain and their numbers decline with age. It is therefore essential to identify new strategies to activate and expand the adult stem cell population. Defects in mitochondria, the energy producing powerhouse of the cells, is associated with neurodegenerative diseases. The impact of mitochondrial impairment in adult stem and progenitor cells in the adult brain remains unknown. Our preliminary data shows that adult stem and progenitor cells are highly sensitive to changes in mitochondrial dynamics and loss of mitochondrial function causes a severe impairment in the development of new neurons in the adult brain. In these studies we will manipulate mitochondrial dynamics in an effort to prevent the decline of adult neurogenesis in the aging brain or in neurodegeneration. The overall goal is develop new treatment strategies by which to regenerate damaged brain tissue.
Competitiondate
201610
Approvedterm2
7 yrs 0 mth
Pinamesdelim
Slack, Ruth S
Approvedterm
7 ans 0 mois
Cihrcontribution2
~ $2,682,655~ $0~