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Grant: Project Grant

University of Alberta

$1,040,400.00

The role of glycosphingolipids in the secretion and clearance of extracellular vesicles in brain health and disease

EF 2020-21

Résumé
Gangliosides are lipid molecules highly enriched in the healthy brain that play important roles in the communication among cells. During ageing and in certain neurodegenerative diseases, levels of gangliosides decrease and contribute to brain dysfunction. Administration of one ganglioside named GM1 has great therapeutic effects in mouse models of Huntington's disease (HD), a neurodegenerative disorder that, like Alzheimer's (AD) and Parkinson's disease (PD) is caused by the accumulation of a toxic protein in the brain. We will investigate the underlying mechanisms with a focus on how GM1 affects the communication between brain cells, brain inflammation and cellular disposal of toxic proteins. Our studies will help determining whether GM1 or similar molecules could be a novel treatment not only for HD but also potentially for AD and PD.
Programme
Project Grant
Bénéficiaire
Emplacement
Alberta, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
433798
Name
Sipione Simonetta
Region
Alberta
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Neurosciences, Mental Health and Addiction
Theme2
Biomedical
Prcname2
Cell and Developmental Physiology
Projecttitle
The role of glycosphingolipids in the secretion and clearance of extracellular vesicles in brain health and disease
Programtype2
Operating Grants
Orgnameinp2
University of Alberta
Cihramount2
$1,040,400
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Animal Models; Biology Of Gangliosides; Cell Models; Extracellular Vesicles; Huntington'S Disease; Microglia; Neurodegeneration; Neuroinflammation; Sialic Acid Binding Proteins
Abstract
Gangliosides are lipid molecules highly enriched in the healthy brain that play important roles in the communication among cells. During ageing and in certain neurodegenerative diseases, levels of gangliosides decrease and contribute to brain dysfunction. Administration of one ganglioside named GM1 has great therapeutic effects in mouse models of Huntington's disease (HD), a neurodegenerative disorder that, like Alzheimer's (AD) and Parkinson's disease (PD) is caused by the accumulation of a toxic protein in the brain. We will investigate the underlying mechanisms with a focus on how GM1 affects the communication between brain cells, brain inflammation and cellular disposal of toxic proteins. Our studies will help determining whether GM1 or similar molecules could be a novel treatment not only for HD but also potentially for AD and PD.
Competitiondate
202010
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Sipione, Simonetta
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $1,040,400~ $0~