Grant: Discovery Grants Program - Individual
Université de Sherbrooke
$64,000.00
Endosomal trafficking and functions in cardiomyocytes: insights from Arf6 signaling
EF 2023-24
Résumé
The long-term vision of our research program is to better understand a fundamental trafficking mechanism that dictate how some proteins reach the surface of contractile cells from the heart, namely the cardiomyocytes. To achieve such goal, we first propose to study, by genetic manipulation of mice, how the removal of a protein named Arf6, an important regulator of protein trafficking in other cells, is impacting heart function. Cell-surface proteins affected by the removal of Arf6 will be further analysed to establish how Arf6 impacts the localization and/or degradation of these proteins and how it affects their function at the membrane of cardiomyocytes. Moreover, we will investigate the role of Arf6 in the genesis and release of cardiac-derived exosomes, which are small vesicles released by cardiomyocytes in their immediate environment and the general circulation before being uptake by other cells. Notably, we will determine how the absence of Arf6 affects the number of exosomes released by cardiomyocytes, but also their protein and miRNA content using unbiased proteomic assays and miRNA screens, respectively. Surprisingly, while this conserved communication system between cells has gained interest in the past years, the mechanisms involved in the production of these exosomes are not yet completely understood. Hence, we expect that our findings will deepen our knowledge about the cardiac endosomal and exosomal trafficking, a fundamental but still enigmatic cellular process in cardiomyocyte's biology. The discoveries originating from this research program will provide benefits to multiple individuals and groups. First, the highly qualified personnel (HQP) formed in my laboratory will benefit from a stimulating research environment. These HQP will become expert in cardiac biology, molecular signaling, genetic manipulation, and related state of the art technology, like echocardiography assessment of murine model, to address the most pressing challenges in the cardiac research field. Also, considering the growing interest in fundamental cardiovascular research and the novel aspects of this research program, we believe our discoveries will generate transposable knowledge that will lead forward the hypothesis and discoveries of other research groups in their own field of expertise.
Programme
Discovery Grants Program - Individual
Bénéficiaire
Emplacement
Quebec, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data
Tel que publié
Application id
RGPIN-2019-06810
Name nom
Auger-Messier, Mannix
Department département
Médecine/cardiologie
Organization id
68
Institution établissement
Université de Sherbrooke
Province en
Québec
Province fr
Québec
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
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
Endosomal trafficking and functions in cardiomyocytes: insights from Arf6 signaling
Keyword
Arf6; Calcium handling with Fura-2 detection; Cardiomyocytes; Confocal microscopy; Endosomal trafficking; Exosomes; Membrane proteins routing and signaling; Quantitative shotgun proteomics; Retromer and retriever complexes; Sorting nexins (SNX)
Application summary
The long-term vision of our research program is to better understand a fundamental trafficking mechanism that dictate how some proteins reach the surface of contractile cells from the heart, namely the cardiomyocytes. To achieve such goal, we first propose to study, by genetic manipulation of mice, how the removal of a protein named Arf6, an important regulator of protein trafficking in other cells, is impacting heart function. Cell-surface proteins affected by the removal of Arf6 will be further analysed to establish how Arf6 impacts the localization and/or degradation of these proteins and how it affects their function at the membrane of cardiomyocytes. Moreover, we will investigate the role of Arf6 in the genesis and release of cardiac-derived exosomes, which are small vesicles released by cardiomyocytes in their immediate environment and the general circulation before being uptake by other cells. Notably, we will determine how the absence of Arf6 affects the number of exosomes released by cardiomyocytes, but also their protein and miRNA content using unbiased proteomic assays and miRNA screens, respectively. Surprisingly, while this conserved communication system between cells has gained interest in the past years, the mechanisms involved in the production of these exosomes are not yet completely understood. Hence, we expect that our findings will deepen our knowledge about the cardiac endosomal and exosomal trafficking, a fundamental but still enigmatic cellular process in cardiomyocyte's biology. The discoveries originating from this research program will provide benefits to multiple individuals and groups. First, the highly qualified personnel (HQP) formed in my laboratory will benefit from a stimulating research environment. These HQP will become expert in cardiac biology, molecular signaling, genetic manipulation, and related state of the art technology, like echocardiography assessment of murine model, to address the most pressing challenges in the cardiac research field. Also, considering the growing interest in fundamental cardiovascular research and the novel aspects of this research program, we believe our discoveries will generate transposable knowledge that will lead forward the hypothesis and discoveries of other research groups in their own field of expertise.