Grant: Discovery Grants Program - Individual
York University
$80,000.00
Regulation of mitochondrial bioenergetics in striated muscle
EF 2023-24
Résumé
The regulation of mitochondrial bioenergetics in striated muscle has received much attention given the importance of muscle physiology to fields like metabolism, integrative physiology, mobility etc. While classic models capture fundamental feedback/feedforward loops that regulate mitochondrial and muscle contraction, an emerging model has implicated the cytoskeleton as a unique regulator of mitochondrial bioenergetics. Consistent with our long-term objectives to uncover novel mechanisms regulating mitochondrial bioenergetics and their relationship with muscle function, we propose to investigate how specific cytoskeletal-mitochondrial interactions modulate striated muscle force, mass and quality. To address this hypothesis, our 5 year plan aims to achieve the following goals: Goal #1: Define how the cytoskeletal components regulate mitochondrial bioenergetics. In vitro and in vivo studies will investigate the effects of altering microtubule and intermediate filament architecture on mitochondrial bioenergetics, whether this alters specific interactions between these cytoskeletal components and the outer membrane voltage dependent anion channel which regulates ADP permeability (a master bioenergetic controller), and how collagen VI in the extracellular matrix (ECM) and cell adhesion to ECM by laminin alters a microtubule-mitochondrial axis of regulating bioenergetics. Goal #2: Understand how cytoskeletal regulation of mitochondrial bioenergetics influences muscle function. In vitro and in vivo studies will determine how the above manipulations of cytoskeletal-mitochondrial interactions regulate muscle force production, quality (necrosis, fibrosis) and mass/atrophy. For both overall Goals, in vitro and in vivo studies will manipulate microtubule, vimentin, collagen VI and laminin in primary cells or single fibres from rodents that are genetically or pharmacologically targeted to modify these proteins. My trainees and I have demonstrated that we have the necessary infrastructure and expertise to conduct the core techniques with long-standing collaborators providing the necessary support on certain methods to ensure the interdisciplinary approach to these studies. The proposed aims will provide novel insight into the basic mechanisms by which cytoskeletal components regulate mitochondrial bioenergetics and striated muscle function. Given that both mitochondrial bioenergetics and striated muscle physiology are connected to many fields, the foundational studies will provide insight to numerous research directions. This plan will also provide comprehensive and diverse training experiences to 6 graduate and >5 undergraduate HQP in the areas of physiology, mitochondrial bioenergetics, cellular and molecular biology, biochemistry, and pharmacology, in addition to transferable skills in leadership, project management, communication and knowledge dissemination that are sought after in all career sectors including industry, academia and government.
Programme
Discovery Grants Program - Individual
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data
Tel que publié
Application id
RGPIN-2019-06687
Name nom
Perry, Christopher
Department département
School of 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
2019
Award amount
80000
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
5502
Research subject group en
Animal biology
Research subject group fr
Kinesiology
Research subject en
Biologie animale
Research subject fr
Kinésiologie
Application title
Regulation of mitochondrial bioenergetics in striated muscle
Keyword
Cytoskeleton; Exercise physiology and exercise adaptation; Mitochondrial function; Muscle atrophy; Muscle damage; Muscle metabolism; Muscle physiology; Muscle weakness; Oxidative stress; Reactive oxygen species
Application summary
The regulation of mitochondrial bioenergetics in striated muscle has received much attention given the importance of muscle physiology to fields like metabolism, integrative physiology, mobility etc. While classic models capture fundamental feedback/feedforward loops that regulate mitochondrial and muscle contraction, an emerging model has implicated the cytoskeleton as a unique regulator of mitochondrial bioenergetics. Consistent with our long-term objectives to uncover novel mechanisms regulating mitochondrial bioenergetics and their relationship with muscle function, we propose to investigate how specific cytoskeletal-mitochondrial interactions modulate striated muscle force, mass and quality. To address this hypothesis, our 5 year plan aims to achieve the following goals: Goal #1: Define how the cytoskeletal components regulate mitochondrial bioenergetics. In vitro and in vivo studies will investigate the effects of altering microtubule and intermediate filament architecture on mitochondrial bioenergetics, whether this alters specific interactions between these cytoskeletal components and the outer membrane voltage dependent anion channel which regulates ADP permeability (a master bioenergetic controller), and how collagen VI in the extracellular matrix (ECM) and cell adhesion to ECM by laminin alters a microtubule-mitochondrial axis of regulating bioenergetics. Goal #2: Understand how cytoskeletal regulation of mitochondrial bioenergetics influences muscle function. In vitro and in vivo studies will determine how the above manipulations of cytoskeletal-mitochondrial interactions regulate muscle force production, quality (necrosis, fibrosis) and mass/atrophy. For both overall Goals, in vitro and in vivo studies will manipulate microtubule, vimentin, collagen VI and laminin in primary cells or single fibres from rodents that are genetically or pharmacologically targeted to modify these proteins. My trainees and I have demonstrated that we have the necessary infrastructure and expertise to conduct the core techniques with long-standing collaborators providing the necessary support on certain methods to ensure the interdisciplinary approach to these studies. The proposed aims will provide novel insight into the basic mechanisms by which cytoskeletal components regulate mitochondrial bioenergetics and striated muscle function. Given that both mitochondrial bioenergetics and striated muscle physiology are connected to many fields, the foundational studies will provide insight to numerous research directions. This plan will also provide comprehensive and diverse training experiences to 6 graduate and >5 undergraduate HQP in the areas of physiology, mitochondrial bioenergetics, cellular and molecular biology, biochemistry, and pharmacology, in addition to transferable skills in leadership, project management, communication and knowledge dissemination that are sought after in all career sectors including industry, academia and government.