Grant: Engage Grants Program
University of Regina
$25,000.00
Use of permeable proteins in defining cell fate in endogenous neural precursor stem cells
FY 2016-17
Summary
Stem cells have the potential to give much insight to both tissue development as well as disease progression. Stem cells have been extensively researched in the context of tissue engineering because of their ability to differentiate into multiple cell lines. However, current methods employed to drive stem cells to specific cell lineages are both challenging and inefficient. Additionally, the source of cells is problematic because typically they have either significant ethical issues (e.g. fetal tissue) or use cells that are unable to stop replicating (e.g. inducible pluritpotent stem cells). Thus there is much interest in better defining and driving endogenous stem cells, without associated ethical or technical issues. This project joins the expertise of the Dr. Buttigieg research team as well as that of iProgen, a biotechnology company, to develop cell permeable transcription factors that can be utilized on endogenous stem cells and thus increase the efficiency of driving cells to particular fates. Two factors to be researched are SOX2 (neuron development) and Olig2 (oligodendroglial development). To date, there are no such permeable protein homologues available, nor are their effects known fully. For this pilot project, iProgen will engineer and produce SOX2 and Olig2 transcription factors. Dr. Buttigieg will then evaluate and characterize the effects of these proteins on endogenous stem cell behaviour. This project represents a first time collaboration between iProgen and the Buttigieg laboratory.
Program
Engage Grants Program
Recipient
Location
Saskatchewan, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data
As published
Application id
499495-2016
Name nom
Buttigieg, Josef
Department département
Biology
Organization id
17
Institution établissement
University of Regina
Province en
Saskatchewan
Province fr
Saskatchewan
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2016
Competition year année de concours
2016
Award amount
25000
Program id
EGP
Program name en
Engage Grants Program
Program name fr
Programme de subventions d'engagement partenariat
Group en
Research partnerships programs
Group fr
Programmes de partenariat
Committee code
1555
Committee name en
Prairie Internal Decision Committee
Committee name fr
Comité de décision interne pour les Prairies
Area of application code
1102
Area of application group en
Health, education and social services
Area of application group fr
Santé publique, éducation et services sociaux
Area of application en
Biomedical engineering
Area of application fr
Génie biomédical
Research subject code
5105
Research subject group en
Cell biology
Research subject group fr
Biologie cellulaire
Research subject en
Cell differentiation
Research subject fr
Différenciation cellulaire
Partie
1
Nb partie
1
Application title
Use of permeable proteins in defining cell fate in endogenous neural precursor stem cells
Keyword
NSERC
Application summary
Stem cells have the potential to give much insight to both tissue development as well as disease progression. Stem cells have been extensively researched in the context of tissue engineering because of their ability to differentiate into multiple cell lines. However, current methods employed to drive stem cells to specific cell lineages are both challenging and inefficient. Additionally, the source of cells is problematic because typically they have either significant ethical issues (e.g. fetal tissue) or use cells that are unable to stop replicating (e.g. inducible pluritpotent stem cells). Thus there is much interest in better defining and driving endogenous stem cells, without associated ethical or technical issues. This project joins the expertise of the Dr. Buttigieg research team as well as that of iProgen, a biotechnology company, to develop cell permeable transcription factors that can be utilized on endogenous stem cells and thus increase the efficiency of driving cells to particular fates. Two factors to be researched are SOX2 (neuron development) and Olig2 (oligodendroglial development). To date, there are no such permeable protein homologues available, nor are their effects known fully. For this pilot project, iProgen will engineer and produce SOX2 and Olig2 transcription factors. Dr. Buttigieg will then evaluate and characterize the effects of these proteins on endogenous stem cell behaviour. This project represents a first time collaboration between iProgen and the Buttigieg laboratory.