Grant: Foundation Grant
University of Toronto
$2,668,274.00
Engineering stem cell fate and function
EF 2016-17
Résumé
Regenerative medicine (RM) offers an opportunity to address the root causes of chronic diseases, which typically result from the breakdown of tissues maintained by stem cells (SC). In Canada, chronic disease consumes 67% of direct health care costs, with approximately $68 billion attributable to treatment costs. Canada is a leader in SC-based RM and my group has contributed to discovery and innovation in this sector.
Early RM technologies focused on the transplantation of cells from the same individual. RM is now at a stage where cell products, such as blood SC, are manufactured for clinical testing. My proposed program is building the next generation of RM therapeutics - living cells and tissues designed to treat specific indications. My vision is to understand, at a fundamental level, the mechanisms by which complex tissues develop from SC, and to use this understanding to advance new cell therapies and regenerative medicines.
Our approach is based on three complementary thrusts. First, we are developing computer simulations of normal and diseased human tissue development. These simulations allow us to connect the genetic coding inside SC to the environment that influences SC growth. These simulations will one day dramatically shorten the time it takes to develop new therapies for degenerative diseases. Second, we are rewiring the genetic code in, and the environment around, SC to understand the key requirements of SC-based tissue development and to increase the quantity and quality of SC-derived cells produced. Third, with our partners, we are moving promising discoveries towards the clinic using advanced models of disease, with a focus on testing specialized blood cells as blood cancer and autoimmune disease therapeutics.
Our work will reveal new rules that govern tissue development, generate new technologies for RM applications, and yield new SC-based therapies. Our work contributes to the CIHR mission to improve the health and welfare of Canadians.
Programme
Foundation Grant
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
355130
Name
Zandstra Peter W
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Genetics
Theme2
Biomedical
Prcname2
Foundation Grant
Projecttitle
Engineering stem cell fate and function
Programtype2
Operating Grants
Orgnameinp2
University of Toronto
Cihramount2
$2,668,274
Cihrequipment2
$0
Programname2
Foundation Grant
Keyworddelim
Blood Development; Cell Reprogramming; Computational Modeling; Hematopoietic Stem Cells; Mesoderm; Microenvironmental Control; Niche Engineering; Pluripotent Stem Cells; Stem Cells
Abstract
Regenerative medicine (RM) offers an opportunity to address the root causes of chronic diseases, which typically result from the breakdown of tissues maintained by stem cells (SC). In Canada, chronic disease consumes 67% of direct health care costs, with approximately $68 billion attributable to treatment costs. Canada is a leader in SC-based RM and my group has contributed to discovery and innovation in this sector.
Early RM technologies focused on the transplantation of cells from the same individual. RM is now at a stage where cell products, such as blood SC, are manufactured for clinical testing. My proposed program is building the next generation of RM therapeutics - living cells and tissues designed to treat specific indications. My vision is to understand, at a fundamental level, the mechanisms by which complex tissues develop from SC, and to use this understanding to advance new cell therapies and regenerative medicines.
Our approach is based on three complementary thrusts. First, we are developing computer simulations of normal and diseased human tissue development. These simulations allow us to connect the genetic coding inside SC to the environment that influences SC growth. These simulations will one day dramatically shorten the time it takes to develop new therapies for degenerative diseases. Second, we are rewiring the genetic code in, and the environment around, SC to understand the key requirements of SC-based tissue development and to increase the quantity and quality of SC-derived cells produced. Third, with our partners, we are moving promising discoveries towards the clinic using advanced models of disease, with a focus on testing specialized blood cells as blood cancer and autoimmune disease therapeutics.
Our work will reveal new rules that govern tissue development, generate new technologies for RM applications, and yield new SC-based therapies. Our work contributes to the CIHR mission to improve the health and welfare of Canadians.
Competitiondate
201610
Approvedterm2
7 yrs 0 mth
Pinamesdelim
Zandstra, Peter W
Approvedterm
7 ans 0 mois
Cihrcontribution2
~ $2,668,274~ $0~