Grant: Doctoral Award - Frederick Banting and Charles Best Canada Graduate Scholarships
University of British Columbia
$105,000.00
Transcriptional Role of Meis1 in Regulating Endothelial-to-Hematopoietic Transition
FY 2016-17
Summary
Hematopoietic stem cell (HSC) transplantation is used to treat a broad range of cancer and blood disorders, mainly leukemia and lymphomas. This therapeutic approach is effective because HSCs are able to produce all the cell types circulating in the blood, which allows the immune system to recover after chemotherapy. There are many challenges associated with HSC transplantation, in particular, their source. HSCs are a rare occurrence and are mainly found in adult bone marrow or umbilical cord blood; this means a limited supply for medical treatment. The need for compatible donor can also delay transplantation procedures. Several groups have tried to make HSC, but these attempts have failed because our current knowledge is insufficient.
The goal of this project is to broaden our understanding of the genes involved in hematopoietic stem cell formation and assist with the production of stem cells for curative strategies. Our preliminary findings reveal that Meis1 gene is highly expressed in cells having the potential to become HSC during development. My data suggests that the absence of Meis1 interferes with the ability to produce stem cells. Therefore I hypothesize that Meis1 plays a key role in promoting hematopoietic stem cell formation. My objectives are to 1) understand the requirement for Meis1 in HSC development and 2) determine which genes are controlled by Meis1 during this process. I will trace and knock-down Meis1 expression with the use mouse models to look at cell fate and gene expression during the normal development of HSC. Ultimately, this study will build knowledge for molecular programming needed to make hematopoietic stem cells for medical treatment, disease modeling, and testing therapies without risking the lives of patients.
Department
Program
Doctoral Award - Frederick Banting and Charles Best Canada Graduate Scholarships
Recipient
Location
British Columbia, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
365435
Name
Coulombe Patrick
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Doctoral Research Awards - A
Projecttitle
Transcriptional Role of Meis1 in Regulating Endothelial-to-Hematopoietic Transition
Programtype2
Studentship Programs
Orgnameinp2
University of British Columbia
Cihramount2
$105,000
Cihrequipment2
$0
Programname2
Doctoral Award - Frederick Banting and Charles Best Canada Graduate Scholarships
Keyworddelim
Developmental Biology; Endothelial-To-Hematopoietic Transition; Gene Regulation; Hematopoiesis; Meis1; Mouse Model; Stem Cell
Abstract
Hematopoietic stem cell (HSC) transplantation is used to treat a broad range of cancer and blood disorders, mainly leukemia and lymphomas. This therapeutic approach is effective because HSCs are able to produce all the cell types circulating in the blood, which allows the immune system to recover after chemotherapy. There are many challenges associated with HSC transplantation, in particular, their source. HSCs are a rare occurrence and are mainly found in adult bone marrow or umbilical cord blood; this means a limited supply for medical treatment. The need for compatible donor can also delay transplantation procedures. Several groups have tried to make HSC, but these attempts have failed because our current knowledge is insufficient.
The goal of this project is to broaden our understanding of the genes involved in hematopoietic stem cell formation and assist with the production of stem cells for curative strategies. Our preliminary findings reveal that Meis1 gene is highly expressed in cells having the potential to become HSC during development. My data suggests that the absence of Meis1 interferes with the ability to produce stem cells. Therefore I hypothesize that Meis1 plays a key role in promoting hematopoietic stem cell formation. My objectives are to 1) understand the requirement for Meis1 in HSC development and 2) determine which genes are controlled by Meis1 during this process. I will trace and knock-down Meis1 expression with the use mouse models to look at cell fate and gene expression during the normal development of HSC. Ultimately, this study will build knowledge for molecular programming needed to make hematopoietic stem cells for medical treatment, disease modeling, and testing therapies without risking the lives of patients.
Competitiondate
201610
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Coulombe, Patrick
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $105,000~ $0~