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Grant: CIHR Fellowship

University of British Columbia

$105,000.00

Cholesterol in islet dysfunction and type 2 diabetes

EF 2008-09

Résumé
Type 2 diabetes affects more than 2 million Canadians, and is a major risk factor for coronary heart disease, the leading cause of death in Canada. Type 2 diabetes results from a relative insufficiency of specific cells in the pancreas ("beta-cells") to produce enough insulin to meet the increasing metabolic demands caused by obesity and ageing. Type 2 diabetes often occurs together with elevated levels of LDL ("bad cholesterol") and low levels of HDL ("good cholesterol"), but the mechanistic connections between cholesterol metabolism and diabetes are poorly understood. We recently discovered that the cholesterol transporter ABCA1, which is crucial for regulating cholesterol levels inside cells, is essential for the normal release of insulin in beta-cells. Mice which lack Abca1 in beta-cells have impaired glucose tolerance due to impaired beta-cell function. The objective of this proposal is to determine the role of ABCA1 in beta-cell function, glucose metabolism and type 2 diabetes. These studies could suggest a novel mechanism for the development of type 2 diabetes and lead to new ways to prevent and treat this disease.
Programme
CIHR Fellowship
Emplacement
British Columbia, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
174054
Name
Kruit Janine K
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Nutrition, Metabolism and Diabetes
Theme2
Biomedical
Prcname2
Fellowships - Post-PhD
Projecttitle
Cholesterol in islet dysfunction and type 2 diabetes
Programtype2
Fellowship Programs
Orgnameinp2
University of British Columbia
Cihramount2
$105,000
Cihrequipment2
$0
Programname2
CIHR Fellowship
Keyworddelim
Abca1; Beta-Cells; Cholesterol Homeostasis; Glucose Homeostasis; Transgenic Mice
Abstract
Type 2 diabetes affects more than 2 million Canadians, and is a major risk factor for coronary heart disease, the leading cause of death in Canada. Type 2 diabetes results from a relative insufficiency of specific cells in the pancreas ("beta-cells") to produce enough insulin to meet the increasing metabolic demands caused by obesity and ageing. Type 2 diabetes often occurs together with elevated levels of LDL ("bad cholesterol") and low levels of HDL ("good cholesterol"), but the mechanistic connections between cholesterol metabolism and diabetes are poorly understood. We recently discovered that the cholesterol transporter ABCA1, which is crucial for regulating cholesterol levels inside cells, is essential for the normal release of insulin in beta-cells. Mice which lack Abca1 in beta-cells have impaired glucose tolerance due to impaired beta-cell function. The objective of this proposal is to determine the role of ABCA1 in beta-cell function, glucose metabolism and type 2 diabetes. These studies could suggest a novel mechanism for the development of type 2 diabetes and lead to new ways to prevent and treat this disease.
Competitiondate
200810
Approvedterm2
2 yrs 4 mths
Pinamesdelim
Kruit, Janine K
Approvedterm
2 ans 4 mois
Cihrcontribution2
~ $105,000~ $0~