Synaptic plasticity is widely regarded as the basis for learning, memory, and our ability to adapt to our surroundings. At the level of single neurons or at the level of human behavior, it is clear that plasticity is more robust when we are young. However there is untapped potential for plasticity, repair and regeneration in the adult mammalian brain, as evidenced by the birth of new neurons in several brain regions. These issues are central to the understanding and potential treatment of neurodevelopmental disorders, autism and mental retardation, as well as conditions that result in neural loss or degeneration such as stroke, epilepsy, brain and spinal cord trauma, Parkinson's disease, and Alzheimer's disease. The long-term goal of this project is to understand the mechanisms of circuit formation at the level of single synapses in the hippocampus. Much experimental effort has been directed at the very early period of neurogenesis, whereas much less is known about the integration of adult-generated neurons into functional networks in the adult brain. As for neural development, understanding the functional integration of new neurons in the adult is a daunting task because of the presumed contribution of hundreds of molecules in a spatially and temporally precise sequence. How does one approach this immense problem in the intact animal, yet gain access to single cells and synapses? This project makes use of a novel transgenic mouse to track the development of dendrites and synapses as new neurons leave their niche, and integrate into the adult circuitry of the dentate gyrus. Preliminary data suggests that this process occurs in distinct stages with a period of limited dendrite outgrowth and exclusively GABAergic synapses, followed weeks later by additional dendritic growth and new excitatory synapses. The project will use electrophysiology and cell imaging to chart the inputs and outputs as new neurons integrate into the adult network, both in normal conditions and following perturbations such as exercise and epileptic seizures. The role of molecules that regulate this stage-specific development will be tested using selective marking with specific promoters in transgenic mice, and viral-mediated gene manipulation in vivo. Assays will use biochemical and molecular methods as well as brain slice physiology. The ability to track these distinct stages will also be used to test the role of cell adhesion molecules in synapse maturation.Project Narrative Many neuropsychiatric illnesses cause loss of nerve cells and/or disruption of connections between nerve cells (synapses). This project takes advantage of a unique mouse model to examine the integration of adult- generated (new) neurons into synaptic networks in the hippocampus, thus providing access at the single nerve cell level to mechanisms of synapse formation, repair and regeneration in the brain. These issues are central to the understanding and potential treatment of neurodevelopmental disorders, autism, mental retardation and mood disorders, as well as conditions that result in neural loss or degeneration such as stroke, epilepsy, brain and spinal cord trauma, Parkinson's disease, and Alzheimer's disease.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
5R01MH046613-20
Application #
7643925
Study Section
Neurodifferentiation, Plasticity, and Regeneration Study Section (NDPR)
Program Officer
Panchision, David M
Project Start
1990-04-01
Project End
2012-06-30
Budget Start
2009-07-01
Budget End
2010-06-30
Support Year
20
Fiscal Year
2009
Total Cost
$346,500
Indirect Cost
Name
Oregon Health and Science University
Department
Neurosciences
Type
Schools of Medicine
DUNS #
096997515
City
Portland
State
OR
Country
United States
Zip Code
97239
Tovar, Kenneth R; Westbrook, Gary L (2017) Modulating synaptic NMDA receptors. Neuropharmacology 112:29-33
Villasana, L E; Westbrook, G L; Schnell, E (2014) Neurologic impairment following closed head injury predicts post-traumatic neurogenesis. Exp Neurol 261:156-62
Vaaga, Christopher E; Borisovska, Maria; Westbrook, Gary L (2014) Dual-transmitter neurons: functional implications of co-release and co-transmission. Curr Opin Neurobiol 29:25-32
Vaaga, Christopher E; Tovar, Kenneth R; Westbrook, Gary L (2014) The IGF-derived tripeptide Gly-Pro-Glu is a weak NMDA receptor agonist. J Neurophysiol 112:1241-5
Perederiy, Julia V; Westbrook, Gary L (2013) Structural plasticity in the dentate gyrus- revisiting a classic injury model. Front Neural Circuits 7:17
Tovar, Kenneth R; McGinley, Matthew J; Westbrook, Gary L (2013) Triheteromeric NMDA receptors at hippocampal synapses. J Neurosci 33:9150-60
Perederiy, Julia V; Luikart, Bryan W; Washburn, Eric K et al. (2013) Neural injury alters proliferation and integration of adult-generated neurons in the dentate gyrus. J Neurosci 33:4754-67
Schnell, Eric; Bensen, Aesoon L; Washburn, Eric K et al. (2012) Neuroligin-1 overexpression in newborn granule cells in vivo. PLoS One 7:e48045
Luikart, Bryan W; Perederiy, Julia V; Westbrook, Gary L (2012) Dentate gyrus neurogenesis, integration and microRNAs. Behav Brain Res 227:348-55
Luikart, Bryan W; Bensen, AeSoon L; Washburn, Eric K et al. (2011) miR-132 mediates the integration of newborn neurons into the adult dentate gyrus. PLoS One 6:e19077

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