Grant: Discovery Grants Program - Individual
York University
$40,000.00
Regulation of angiogenesis in skeletal muscle
FY 2023-24
Summary
The major goal of the research performed in my laboratory is to discover novel strategies for controlling blood vessel formation in skeletal muscle. Growth of new blood vessels is a normal healthy response that enables our muscles to adapt appropriately to varying energy demands, including the storage and use of dietary fats. In the short term, an excess of dietary fat promotes beneficial adaptations in the skeletal muscle, to help store and use the excess fat. Such adaptations often include the growth of new blood vessels, to help with the delivery of the energy to the muscle cells. However the signals that coordinate this response in healthy individuals are not known. My research group will focus on defining the relationship between short term fat excess and the regulation of blood vessel growth in skeletal muscle. Second, we will evaluate the potential role of a cell that resides between blood vessels and skeletal muscle cells, the pericyte, as an important coordinator of the adaptive responses to excess dietary fat. We will investigate the function of the protein leptin as an important communicating signal that is produced and released from pericytes to coordinate adaptations in muscle cells and blood vessels. A strength and uniqueness of this project is the combination of approaches that we will employ (both mouse and human muscle, and cell culture models), which will allow us to uncover unique evidence of the regulation of blood vessel growth by fat excess, and the importance of pericytes in coordinating this response. Overall, this research will identify novel targets that may be tested in the future for their capacity to enhance blood vessel growth in skeletal muscle.
Program
Discovery Grants Program - Individual
Recipient
Location
Ontario, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data
As published
Application id
RGPIN-2018-05858
Name nom
Haas, Tara
Department département
Kinesiology and Health Science
Organization id
38
Institution établissement
York University
Province en
Ontario
Province fr
Ontario
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2023
Competition year année de concours
2018
Award amount
40000
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
1502
Committee name en
Biological Systems and Functions
Committee name fr
Systèmes et fonctions biologiques
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
5111
Research subject group en
Cell biology
Research subject group fr
Signal transduction
Research subject en
Biologie cellulaire
Research subject fr
Transduction de signal
Application title
Regulation of angiogenesis in skeletal muscle
Keyword
confocal microscopy; endothelial cell; growth factor signaling; paracrine signaling; transcriptional regulation
Application summary
The major goal of the research performed in my laboratory is to discover novel strategies for controlling blood vessel formation in skeletal muscle. Growth of new blood vessels is a normal healthy response that enables our muscles to adapt appropriately to varying energy demands, including the storage and use of dietary fats. In the short term, an excess of dietary fat promotes beneficial adaptations in the skeletal muscle, to help store and use the excess fat. Such adaptations often include the growth of new blood vessels, to help with the delivery of the energy to the muscle cells. However the signals that coordinate this response in healthy individuals are not known. My research group will focus on defining the relationship between short term fat excess and the regulation of blood vessel growth in skeletal muscle. Second, we will evaluate the potential role of a cell that resides between blood vessels and skeletal muscle cells, the pericyte, as an important coordinator of the adaptive responses to excess dietary fat. We will investigate the function of the protein leptin as an important communicating signal that is produced and released from pericytes to coordinate adaptations in muscle cells and blood vessels. A strength and uniqueness of this project is the combination of approaches that we will employ (both mouse and human muscle, and cell culture models), which will allow us to uncover unique evidence of the regulation of blood vessel growth by fat excess, and the importance of pericytes in coordinating this response. Overall, this research will identify novel targets that may be tested in the future for their capacity to enhance blood vessel growth in skeletal muscle.