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Grant: Discovery Grants Program - Individual

University of Manitoba

$64,000.00

Modulation of cell death and differentiation by myocardin-regulated microRNAs during mammalian development

EF 2023-24

Résumé
During cardiovascular development, the heart and its outflow tract are derived from precursor cells that reside within the embryo. My laboratory is particularly interested in how these precursor cells can become cardiac myocytes of the heart and vascular smooth muscle cells (VSMCs) of the outflow tract. This process of specialization is called differentiation and the molecular mechanisms that regulate differentiation in the heart and outflow tract remain incompletely understood. The process of differentiation is partly opposed by programmed cell death, which is a term used to describe the removal of cells that are no longer necessary. This process is regulated by the Bcl-2 family of proteins. Data from my laboratory has shown that myocardin, which has a critical role in cardiac and VSMC differentiation, can affect both myocyte differentiation and oppose cell death through the expression of microRNAs, which in turn inhibit the pro-death Bcl-2 family members, called Bnip3 and Bnip3L (i.e. Nix). Cell death and differentiation of cardiac and vascular smooth muscle cells is the central focus of my research program. In the next 5-year cycle, my group will determine how myocardin regulates cell death and differentiation, and how Bnip3 and Nix are regulated by signaling pathways. My HQP use innovative and mechanistic cell and molecular biology techniques, including human induced pluripotent stem cells (iPSCs) that can be differentiated into cardiomyocytes and VSMCs using commercially available media. In addition, we use primary rodent cardiomyocytes and vascular smooth muscle cells, and immortalized cells lines to work out the molecular details of our experiments and develop more advanced cell culture skills of trainees working in my laboratory. I predict that 3 PhD students and 3 MSc students will graduate from my lab over the next 5-years. The scientific community's keen interest in stem cell biology strongly suggests that knowledge regarding the mechanisms by which cardiac and VSMCs differentiate from precursor cells will be sought after by cardiovascular physiologists and developmental biologists investigating more applied aspects of this field. Furthermore, my laboratory has considerable experience dissecting the control processes that regulate cell death and differentiation, while maintaining a strong commitment to graduate student training. Collectively, this proposed program of research is feasible, significant, and consistent with the mandate of NSERC.
Programme
Discovery Grants Program - Individual
Emplacement
Manitoba, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data

Tel que publié

Application id
RGPIN-2019-05409
Name nom
Gordon, Joseph
Department département
Faculty of Health Science/Nursing
Organization id
19
Institution établissement
University of Manitoba
Province en
Manitoba
Province fr
Manitoba
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2023
Competition year année de concours
2019
Award amount
64000
Program id
RGPIN
Program name en
Discovery Grants Program - Individual
Program name fr
Programme de subventions à la découverte - individuelles
Group en
DISCOVERY RESEARCH
Group fr
RECHERCHE AXÉE SUR 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
5400
Research subject group en
Biochemistry
Research subject group fr
Biochemistry
Research subject en
Biochimie
Research subject fr
Biochimie
Application title
Modulation of cell death and differentiation by myocardin-regulated microRNAs during mammalian development
Keyword
cardiomyocytes; cell death; differentiation; microRNA; mitochondria; myocardin; vascular smooth muscle cells
Application summary
During cardiovascular development, the heart and its outflow tract are derived from precursor cells that reside within the embryo. My laboratory is particularly interested in how these precursor cells can become cardiac myocytes of the heart and vascular smooth muscle cells (VSMCs) of the outflow tract. This process of specialization is called differentiation and the molecular mechanisms that regulate differentiation in the heart and outflow tract remain incompletely understood. The process of differentiation is partly opposed by programmed cell death, which is a term used to describe the removal of cells that are no longer necessary. This process is regulated by the Bcl-2 family of proteins. Data from my laboratory has shown that myocardin, which has a critical role in cardiac and VSMC differentiation, can affect both myocyte differentiation and oppose cell death through the expression of microRNAs, which in turn inhibit the pro-death Bcl-2 family members, called Bnip3 and Bnip3L (i.e. Nix). Cell death and differentiation of cardiac and vascular smooth muscle cells is the central focus of my research program. In the next 5-year cycle, my group will determine how myocardin regulates cell death and differentiation, and how Bnip3 and Nix are regulated by signaling pathways. My HQP use innovative and mechanistic cell and molecular biology techniques, including human induced pluripotent stem cells (iPSCs) that can be differentiated into cardiomyocytes and VSMCs using commercially available media. In addition, we use primary rodent cardiomyocytes and vascular smooth muscle cells, and immortalized cells lines to work out the molecular details of our experiments and develop more advanced cell culture skills of trainees working in my laboratory. I predict that 3 PhD students and 3 MSc students will graduate from my lab over the next 5-years. The scientific community's keen interest in stem cell biology strongly suggests that knowledge regarding the mechanisms by which cardiac and VSMCs differentiate from precursor cells will be sought after by cardiovascular physiologists and developmental biologists investigating more applied aspects of this field. Furthermore, my laboratory has considerable experience dissecting the control processes that regulate cell death and differentiation, while maintaining a strong commitment to graduate student training. Collectively, this proposed program of research is feasible, significant, and consistent with the mandate of NSERC.