Grant: Discovery Grants Program - Individual
Wilfrid Laurier University
$24,936.00
Gene expression as a critical indicator of hippocampal function
FY 2010-11
Summary
One of the greatest challenges facing neuroscience is to understand the cellular basis of cognition, which critically requires identifying neural activity patterns over widespread regions of the brain. Functional imaging methods (e.g., PET, fMRI) provide low spatiotemporal resolution across the brain; while microelectrode recordings provide precise resolution, but with limited sampling capabilities. What has been missing, until recently, is a method revealing functional activity during multiple epochs of behavior with cellular resolution - a problem recently solved by visualizing immediate-early genes (IEGs). When neurons engage in high frequency activity, they transcribe IEGs which are immediately visible within the nucleus. Subsequently (~30 min), the mRNA is translocated to the cytoplasm. Because mRNA can be resolved in two cellular compartments, it is possible to identify active neurons during two behavioral epochs in the same animal. Thus, like fMRI or PET, IEGs provides repeated activity measurements in the same subject, but with the cellular resolution to delineate neural networks engaged in specific behaviors. During spatial exploration, hippocampal cells fire in distinct physical locations, collectively creating an environment-specific ""map"" thought to establish the context of an episode to be remembered. These cells also reliably transcribe IEGs, permitting estimates of the size/consistency of place maps comparable to direct neuronal recording. Unlike direct recordings, however, IEG expression permits a limitless sample of precisely how many cells are engaged in an environment, and how the size/consistency of active populations change with the environment. Thus, the current grant capitalizes on the unique advantages of using IEG expression to (1) create estimates of how the number of active cells during (1) behavior and (2) subsequent memory-related processing change according to the physical characteristics of the environment (e.g., size/complexity of the environment) as well as (3) how these changes relate to learning. These studies provide critical data on the information that most reliably influences hippocampal activity and provide insight into the nature of the computations that define behavioral context.
Program
Discovery Grants Program - Individual
Recipient
Location
Ontario, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data
As published
Application id
355838-2008
Name nom
Marrone, DianoFabio
Department département
Psychology
Organization id
35
Institution établissement
Wilfrid Laurier University
Province en
Ontario
Province fr
Ontario
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2010
Competition year année de concours
2008
Award amount
24936
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
12
Committee name en
Psychology: Brain, Behaviour & Cognitive Sciences
Committee name fr
Psychologie: Cerveau, comportement et science cognitive
Area of application code
1210
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Psychology
Area of application fr
Psychologie
Research subject code
6308
Research subject group en
Psychology
Research subject group fr
Psychologie
Research subject en
Behavioural neuroscience
Research subject fr
Neurologie du comportement
Partie
3
Nb partie
5
Application title
Gene expression as a critical indicator of hippocampal function
Keyword
NSERC
Application summary
One of the greatest challenges facing neuroscience is to understand the cellular basis of cognition, which critically requires identifying neural activity patterns over widespread regions of the brain. Functional imaging methods (e.g., PET, fMRI) provide low spatiotemporal resolution across the brain; while microelectrode recordings provide precise resolution, but with limited sampling capabilities. What has been missing, until recently, is a method revealing functional activity during multiple epochs of behavior with cellular resolution - a problem recently solved by visualizing immediate-early genes (IEGs). When neurons engage in high frequency activity, they transcribe IEGs which are immediately visible within the nucleus. Subsequently (~30 min), the mRNA is translocated to the cytoplasm. Because mRNA can be resolved in two cellular compartments, it is possible to identify active neurons during two behavioral epochs in the same animal. Thus, like fMRI or PET, IEGs provides repeated activity measurements in the same subject, but with the cellular resolution to delineate neural networks engaged in specific behaviors. During spatial exploration, hippocampal cells fire in distinct physical locations, collectively creating an environment-specific ""map"" thought to establish the context of an episode to be remembered. These cells also reliably transcribe IEGs, permitting estimates of the size/consistency of place maps comparable to direct neuronal recording. Unlike direct recordings, however, IEG expression permits a limitless sample of precisely how many cells are engaged in an environment, and how the size/consistency of active populations change with the environment. Thus, the current grant capitalizes on the unique advantages of using IEG expression to (1) create estimates of how the number of active cells during (1) behavior and (2) subsequent memory-related processing change according to the physical characteristics of the environment (e.g., size/complexity of the environment) as well as (3) how these changes relate to learning. These studies provide critical data on the information that most reliably influences hippocampal activity and provide insight into the nature of the computations that define behavioral context.