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Grant: Discovery Grants Program - Individual

University of Western Ontario

$48,000.00

Role of fibrin-integrin interactions in supporting 2D and 3D pancreatic islet growth and function

EF 2011-12

Résumé
The discovery of insulin in 1921 by Banting and Best laid the foundation for the modern management of diabetes mellitus. However, insulin treatment cannot cure diabetes and will not prevent the secondary complications that are responsible for the devastating morbidity and mortality of this disease. Replacement of insulin-producing cells through islet transplantation has the best chance to prevent, reverse or stabilize these complications. However, the scarcity of islets and limitations in our knowledge of the factors influencing islet biology present a major obstacle precluding islet transplantation from being adopted as a routine treatment. Advancement in this field requires a thorough understanding of the developmental biology of the pancreas. In the present application we propose to identify specific factors that are responsible for the maintenance of insulin-producing cells. Our focus is on the role of integrins, membrane receptors that are known to interact with extracellular matrix proteins to control several aspects of pancreatic organogenesis and tissue maintenance. We will characterize these receptors on insulin-producing cells, examine their interactions with one specific matrix protein, fibrin, and study the mechanisms by which these interactions regulate survival of insulin-producing cells. It is our hope that these studies will facilitate the development of appropriate tissue engineering strategies for a bioartificial endocrine pancreas. This treatment will have far-reaching economic and social benefits.
Programme
Discovery Grants Program - Individual
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data

Tel que publié

Application id
239981-2011
Name nom
Wang, Rennian
Department département
Physiology and Pharmacology
Organization id
36
Institution établissement
University of Western Ontario
Province en
Ontario
Province fr
Ontario
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2011
Competition year année de concours
2011
Award amount
48000
Program id
RGPIN
Program nane en
Discovery Grants Program - Individual
Program name fr
Programme de subventions à la découverte - individuelles
Group en
Discovery grants programs
Group fr
Programmes de subventions à la découverte
Committee code
1501
Committee name en
Genes, Cells and Molecules
Committee name fr
Gènes, cellules et molécules
Area of application code
1201
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Life sciences (including biotechnology)
Area of application fr
Sciences de la vie (y compris biotechnologie)
Research subject code
5100
Research subject group en
Cell biology
Research subject group fr
Biologie cellulaire
Research subject en
Cell biology
Research subject fr
Biologie cellulaire
Partie
1
Nb partie
5
Application title
Role of fibrin-integrin interactions in supporting 2D and 3D pancreatic islet growth and function
Keyword
NSERC
Application summary
The discovery of insulin in 1921 by Banting and Best laid the foundation for the modern management of diabetes mellitus. However, insulin treatment cannot cure diabetes and will not prevent the secondary complications that are responsible for the devastating morbidity and mortality of this disease. Replacement of insulin-producing cells through islet transplantation has the best chance to prevent, reverse or stabilize these complications. However, the scarcity of islets and limitations in our knowledge of the factors influencing islet biology present a major obstacle precluding islet transplantation from being adopted as a routine treatment. Advancement in this field requires a thorough understanding of the developmental biology of the pancreas. In the present application we propose to identify specific factors that are responsible for the maintenance of insulin-producing cells. Our focus is on the role of integrins, membrane receptors that are known to interact with extracellular matrix proteins to control several aspects of pancreatic organogenesis and tissue maintenance. We will characterize these receptors on insulin-producing cells, examine their interactions with one specific matrix protein, fibrin, and study the mechanisms by which these interactions regulate survival of insulin-producing cells. It is our hope that these studies will facilitate the development of appropriate tissue engineering strategies for a bioartificial endocrine pancreas. This treatment will have far-reaching economic and social benefits.