Grant: Project Grant
McGill University
$914,175.00
Brain Energy Supply in Alzheimer's disease
EF 2020-21
Résumé
The principal energy fuel of the brain is sugar. From the bloodstream, sugars are taken up by the cells of the blood vessels and are then further provided to cells in the brain. Specialized transport proteins are needed for the sugar uptake, the most important transporter in the brain is glucose transporter 1 (GLUT1). In the most common neurodegenerative disorder, Alzheimer's disease, the amount of GLUT1 transporters is much lower and the affected brains utilize less glucose as compared to healthy controls. Consequently, the restriction of energy to the brain itself may contribute to neurodegeneration. It is therefore imperative to understand how GLUT1 is regulated at the molecular level. My laboratory discovered a novel GLUT1-regulating mechanism inside the cell. We aim to understand this mechanism in detail to learn if this molecular pathway could be used to ameliorate Alzheimer's disease
symptoms.
Programme
Project Grant
Bénéficiaire
Emplacement
Quebec, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
435836
Name
Münter Lisa M
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Genetics
Theme2
Biomedical
Prcname2
Cell Biology - Molecular/Fundamental
Projecttitle
Brain Energy Supply in Alzheimer's disease
Programtype2
Operating Grants
Orgnameinp2
McGill University
Cihramount2
$914,175
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Adeno-Associated Virus (Aav); Alzheimer'S Disease; Amyloid Precursor Protein, App; Cerebral Glucose Uptake; Endothelial Cells; Glucose Transporter 1, Glut1; Hypoxia; Microtubule-Associated Protein Tau; Rhomboid Protease; Ubiquitin
Abstract
The principal energy fuel of the brain is sugar. From the bloodstream, sugars are taken up by the cells of the blood vessels and are then further provided to cells in the brain. Specialized transport proteins are needed for the sugar uptake, the most important transporter in the brain is glucose transporter 1 (GLUT1). In the most common neurodegenerative disorder, Alzheimer's disease, the amount of GLUT1 transporters is much lower and the affected brains utilize less glucose as compared to healthy controls. Consequently, the restriction of energy to the brain itself may contribute to neurodegeneration. It is therefore imperative to understand how GLUT1 is regulated at the molecular level. My laboratory discovered a novel GLUT1-regulating mechanism inside the cell. We aim to understand this mechanism in detail to learn if this molecular pathway could be used to ameliorate Alzheimer's disease
symptoms.
Competitiondate
202010
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Münter, Lisa M
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $914,175~ $0~