Learning and memory defines how animals interact with their environment. This process relies on experience-driven changes in synaptic connections, a phenomenon known as synaptic plasticity; disruption of this process is believed to underlie several cognitive and psychiatric disorders. Although synaptic plasticity is critical for learning and memory, the mechanisms by which memory is formed and stored in neural circuits remains poorly understood. The proposed studies address this knowledge gap by focusing on synaptic mechanisms by which contextual memory is encoded in CA3 pyramidal neurons of the hippocampus, a brain region with a central role in learning and memory. Among the excitatory inputs converging onto CA3 pyramidal neurons, the mossy fiber (MF) input from dentate gyrus granule cells is known to be required for the encoding of contextual memory. Using genetic tools recently developed by us, we were able to identify the specific group of CA3 neurons activated by contextual learning, and identified a learning-dependent synaptic modifications associated with these neurons. We hypothesize that this newly identified synaptic plasticity plays a critical role in contextual memory formation. This hypothesis will be tested using a combination of molecular, cellular, electrophysiological and behavioral approaches in mice. We will also identify molecular pathways that selectively modulate MF-CA3 synapses in the mouse hippocampus. The proposed research has the potential to generate conceptual breakthroughs in our molecular and cellular understanding of memory formation, and ultimately provide insights into mechanisms underlying cognitive and psychiatric impairments.

Public Health Relevance

The research described in this proposal will allow us to understand how sensory and behavioral experience is processed at the cellular and synaptic level and converted into long-lasting behavioral changes. It will have a tremendous impact on our understanding on how animals interact with their environment, disruption of which underlies many cognitive and psychiatric disorders.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
1R01MH116673-01A1
Application #
9687812
Study Section
Synapses, Cytoskeleton and Trafficking Study Section (SYN)
Program Officer
Driscoll, Jamie
Project Start
2018-12-01
Project End
2023-11-30
Budget Start
2018-12-01
Budget End
2019-11-30
Support Year
1
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Massachusetts Institute of Technology
Department
Other Basic Sciences
Type
Schools of Arts and Sciences
DUNS #
001425594
City
Cambridge
State
MA
Country
United States
Zip Code
02142