Grant: Project Grant
University of Toronto
$914,175.00
Strains of alpha-synuclein aggregates as drivers of disease heterogeneity in Parkinson's disease and related disorders
EF 2019-20
Résumé
Parkinson's disease (PD) is a devastating, incurable disease of the ageing brain. More than 100,000 Canadians currently suffer from PD, and this number is expected to increase in the near future due to an ageing population. In PD, a protein called alpha-synuclein clumps together in the brain to form aggregates. These aggregates are believed to cause the death of brain cells, which produces the symptoms of PD. A recent breakthrough has revealed that alpha-synuclein aggregates share many similarities with prions, including the ability to spread between cells in the brain. Prions are improperly shaped, infectious proteins that cause brain diseases such as Creutzfeldt-Jakob disease and "mad cow disease". Similar to bacteria and viruses, prions can exist as distinct strains that cause variability in disease symptoms and pathology. The goal of this research is to use genetically modified mice to establish whether alpha-synuclein aggregates can also exist as different strains. In particular, we are interested in determining whether different strains of alpha-synuclein aggregates cause different diseases in mice. The results of these studies will help to clarify whether different strains of alpha-synuclein aggregates are responsible for the patient-to-patient variability observed in PD and related diseases, and will provide improved animal models for testing candidate therapeutics for PD.
Programme
Project Grant
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
408498
Name
Watts Joel C
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Aging
Theme2
Biomedical
Prcname2
Molecular & Cellular Neurosciences - B
Projecttitle
Strains of alpha-synuclein aggregates as drivers of disease heterogeneity in Parkinson's disease and related disorders
Programtype2
Operating Grants
Orgnameinp2
University of Toronto
Cihramount2
$914,175
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Dementia With Lewy Bodies; Multiple System Atrophy; Neurodegeneration; Parkinson'S Disease; Prions; Protein Aggregation; Protein Misfolding; Seeding; Strains; Transgenic Mice
Abstract
Parkinson's disease (PD) is a devastating, incurable disease of the ageing brain. More than 100,000 Canadians currently suffer from PD, and this number is expected to increase in the near future due to an ageing population. In PD, a protein called alpha-synuclein clumps together in the brain to form aggregates. These aggregates are believed to cause the death of brain cells, which produces the symptoms of PD. A recent breakthrough has revealed that alpha-synuclein aggregates share many similarities with prions, including the ability to spread between cells in the brain. Prions are improperly shaped, infectious proteins that cause brain diseases such as Creutzfeldt-Jakob disease and "mad cow disease". Similar to bacteria and viruses, prions can exist as distinct strains that cause variability in disease symptoms and pathology. The goal of this research is to use genetically modified mice to establish whether alpha-synuclein aggregates can also exist as different strains. In particular, we are interested in determining whether different strains of alpha-synuclein aggregates cause different diseases in mice. The results of these studies will help to clarify whether different strains of alpha-synuclein aggregates are responsible for the patient-to-patient variability observed in PD and related diseases, and will provide improved animal models for testing candidate therapeutics for PD.
Competitiondate
201909
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Watts, Joel C
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $914,175~ $0~