Grant: Project Grant
McGill University
$1,101,600.00
Role of Mitochondrial Import and Processing of PINK1 in Parkinson Disease
FY 2023-24
Summary
Parkinson's disease (PD) affects over 100,000 people in Canada and the numbers will only grow as the population ages. PD involves the death of dopamine neurons in the midbrain, which leads to devastating motor and functional impairment. Although treatment is available, its effectiveness diminishes over the long term. Hope for a more definitive treatment lies in basic biomedical research. Already, important advances have been made using molecular and genetic approaches. Over the past three decades, several genes have been identified which cause familial forms of PD or increase the risk of sporadic PD. My laboratory has a longstanding interest in understanding the normal function of these PD genes and how defects in the genes lead to PD. Work over the past 15 years has led to the discovery that several of these genes converge on mitochondria, the cell's energy power plant, and a focal point of the degenerative process in PD. The aim of this application is to decipher how one of these PD genes, PINK1 impacts mitochondrial function normally and what goes wrong in disease.
Department
Program
Project Grant
Recipient
Location
Quebec, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
500195
Name
Fon Edward A
Region
Québec
Country
Canada
Orgtype
Research Institution; Institution Paid
Instname2
Neurosciences, Mental Health and Addiction
Theme2
Biomedical
Prcname2
Cell Biology - Disease 2
Projecttitle
Role of Mitochondrial Import and Processing of PINK1 in Parkinson Disease
Programtype2
Operating Grants
Orgnameinp2
McGill University
Cihramount2
$1,101,600
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Ipscs; Mitochondria; Mitophagy; Neurodegeneration; Parkin; Parkinson Disease; Pink1; Ubiquitin
Abstract
Parkinson's disease (PD) affects over 100,000 people in Canada and the numbers will only grow as the population ages. PD involves the death of dopamine neurons in the midbrain, which leads to devastating motor and functional impairment. Although treatment is available, its effectiveness diminishes over the long term. Hope for a more definitive treatment lies in basic biomedical research. Already, important advances have been made using molecular and genetic approaches. Over the past three decades, several genes have been identified which cause familial forms of PD or increase the risk of sporadic PD. My laboratory has a longstanding interest in understanding the normal function of these PD genes and how defects in the genes lead to PD. Work over the past 15 years has led to the discovery that several of these genes converge on mitochondria, the cell's energy power plant, and a focal point of the degenerative process in PD. The aim of this application is to decipher how one of these PD genes, PINK1 impacts mitochondrial function normally and what goes wrong in disease.
Competitiondate
202403
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Fon, Edward A
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $1,101,600~ $0~