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Grant: Discovery Grants Program - Individual

Université de Sherbrooke

$64,000.00

Mechanisms of experience-dependent hippocampal neurogenesis

EF 2020-21

Résumé
My NSERC-funded research program tackles the question of how life experience shapes brain structure and function. Plasticity, or the ability to be dynamically changed by life experience, is one of the brain's defining features. The production of new neurons by neural stem cells in the hippocampus, a structure involved in learning, memory and emotion, is one such form of plasticity. By focusing on this process of hippocampal neurogenesis, our long-term goal is to develop an integrated model, from behaviour to genes, of how life experience regulates brain function. Mice are a simple but powerful mammalian model for studying this question, as their living environments can be tightly controlled, they can be used for genetic manipulations to test specific hypotheses, and their brain function can be measured using tests of learning, memory and emotion. Mice housed in an enriched environment (EE) have better learning and memory and more hippocampal neurogenesis, but it has long been unclear what EE elements are responsible (Physical exercise? Cognitive challenges? Social hierarchies? Stress? Sensory stimulation?). In the preceding stage of this research program, my trainees overcame this major hurdle, developing a novel EE strategy that successfully separates the impact of such factors (our first major goal). We are now testing whether each of these factors contributes to changes in learning, memory and/or emotions. Our second major goal is to identify genetic changes occurring at the level of the hippocampus itself in response to each EE factor. My PhD and postdoc students are collaborating using cutting-edge genetic and mass spectrometry approaches to uncover the local mediators of change in hippocampal function. Our third major goal is to then identify the circulating signals by which an enriched environment “talks” to the hippocampus to trigger these genetic changes. My first postdoc student is testing the specific hypothesis that EE-induced hormonal fluctuations are systemic mediators of neurogenesis changes. Our research program will generate fundamental insights into environment-brain interactions. These studies will provide an integrated, multi-level analysis that links life experiences to changes in brain gene expression and stem cell activity. HQP will receive training that is diverse, from the behavioural to the genetic levels, representing valuable, specialized and versatile expertise for positions in academia, stem cell industry, and government regulation.
Programme
Discovery Grants Program - Individual
Emplacement
Quebec, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data

Tel que publié

Application id
RGPIN-2016-04839
Name nom
Fernandes, Karl
Department département
Medicine/Neurology
Organization id
68
Institution établissement
Université de Sherbrooke
Province en
Québec
Province fr
Québec
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2020
Competition year année de concours
2016
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 grants programs
Group fr
Programmes de subventions à la découverte
Committee code
1501
Committee name en
Genes, Cells and Molecules
Committee name fr
Gènes, cellules et molécules
Area of application code
1200
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Advancement of knowledge
Area of application fr
Avancement des connaissances
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
Installment
inst:5-6
Partie
2
Nb partie
6
Application title
Mechanisms of experience-dependent hippocampal neurogenesis
Keyword
NSERC
Application summary
My NSERC-funded research program tackles the question of how life experience shapes brain structure and function. Plasticity, or the ability to be dynamically changed by life experience, is one of the brain's defining features. The production of new neurons by neural stem cells in the hippocampus, a structure involved in learning, memory and emotion, is one such form of plasticity. By focusing on this process of hippocampal neurogenesis, our long-term goal is to develop an integrated model, from behaviour to genes, of how life experience regulates brain function. Mice are a simple but powerful mammalian model for studying this question, as their living environments can be tightly controlled, they can be used for genetic manipulations to test specific hypotheses, and their brain function can be measured using tests of learning, memory and emotion. Mice housed in an enriched environment (EE) have better learning and memory and more hippocampal neurogenesis, but it has long been unclear what EE elements are responsible (Physical exercise? Cognitive challenges? Social hierarchies? Stress? Sensory stimulation?). In the preceding stage of this research program, my trainees overcame this major hurdle, developing a novel EE strategy that successfully separates the impact of such factors (our first major goal). We are now testing whether each of these factors contributes to changes in learning, memory and/or emotions. Our second major goal is to identify genetic changes occurring at the level of the hippocampus itself in response to each EE factor. My PhD and postdoc students are collaborating using cutting-edge genetic and mass spectrometry approaches to uncover the local mediators of change in hippocampal function. Our third major goal is to then identify the circulating signals by which an enriched environment “talks” to the hippocampus to trigger these genetic changes. My first postdoc student is testing the specific hypothesis that EE-induced hormonal fluctuations are systemic mediators of neurogenesis changes. Our research program will generate fundamental insights into environment-brain interactions. These studies will provide an integrated, multi-level analysis that links life experiences to changes in brain gene expression and stem cell activity. HQP will receive training that is diverse, from the behavioural to the genetic levels, representing valuable, specialized and versatile expertise for positions in academia, stem cell industry, and government regulation.