Grant: Operating Grant
University of Toronto
$675,050.00
Characterization of human embryonic stem cell- and adult pancreatic multipotent precursor-derived beta cells.
EF 2010-11
Résumé
Type 1 diabetes is a devastating disease that causes reduced quality and length of life in humans. Treatments that aim to correct the loss of insulin-secreting pancreatic beta cells in type 1 diabetes traditionally involve multiple daily injections of insulin and recently transplantation of cells from donors. However, both regimens have their drawbacks as they are invasive and supply of donor tissue is limited. Therefore the generation of beta cells from human stem cells from either embryonic or adult tissue, represents a potentially unlimited supply of beta cells to treat this debilitating disease. Our collaborators have successfully generated beta-like cells from human embryonic and adult human pancreatic tissue but these cells have yet to be fully characterised for their insulin secreting potential. Therefore, this grant aims to determine the expression profile of hormones, including insulin, in these two stem cell populations and see whether they secrete insulin normally when stimulated with glucose. Beta cells contain very specialised glucose sensing machinery within them and we propose to establish which parts of this machinery are defective in the stem cell-derived beta cells. Finally we will examine the pattern of genes and proteins that are expressed in pure populations of stem cell-derived beta cells. The information gained from these studies will help to generate strategies to improve the production of beta cells from different sources of stem cells to be used in the treatment of type 1 diabetes.
Programme
Operating Grant
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
211239
Name
Wheeler Michael B
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Nutrition, Metabolism and Diabetes
Theme2
Biomedical
Prcname2
Diabetes, Obesity, Lipid & Lipoprotein Disorders
Projecttitle
Characterization of human embryonic stem cell- and adult pancreatic multipotent precursor-derived beta cells.
Programtype2
Operating Grants
Orgnameinp2
University of Toronto
Cihramount2
$675,050
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Adult Pancreatic Derived Stem Cells; Beta Cells; Gene Array; Glucose Metabolism; Human Embryonic Stem Cells; Induced Pluripotent Stem Cells; Insulin Secretion; Islet; Proteomics; Type 1 Diabetes
Abstract
Type 1 diabetes is a devastating disease that causes reduced quality and length of life in humans. Treatments that aim to correct the loss of insulin-secreting pancreatic beta cells in type 1 diabetes traditionally involve multiple daily injections of insulin and recently transplantation of cells from donors. However, both regimens have their drawbacks as they are invasive and supply of donor tissue is limited. Therefore the generation of beta cells from human stem cells from either embryonic or adult tissue, represents a potentially unlimited supply of beta cells to treat this debilitating disease. Our collaborators have successfully generated beta-like cells from human embryonic and adult human pancreatic tissue but these cells have yet to be fully characterised for their insulin secreting potential. Therefore, this grant aims to determine the expression profile of hormones, including insulin, in these two stem cell populations and see whether they secrete insulin normally when stimulated with glucose. Beta cells contain very specialised glucose sensing machinery within them and we propose to establish which parts of this machinery are defective in the stem cell-derived beta cells. Finally we will examine the pattern of genes and proteins that are expressed in pure populations of stem cell-derived beta cells. The information gained from these studies will help to generate strategies to improve the production of beta cells from different sources of stem cells to be used in the treatment of type 1 diabetes.
Competitiondate
201009
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Wheeler, Michael B
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $675,050~ $0~