The dendritic trees of neurons in the brain's cortex conduct elemental brain functions such as information processing and learning. Research in brain slices has provided a wealth of information about the dendritic mechanisms that could be operating in behaving animals to integrate, and alter the strength of, synaptic inputs from presynaptic sources. Key among these mechanisms are back-propagating action potentials and nonlinear integration of synaptic inputs leading to dendritic spiking, which confer to the dendritic tree a host of local and global plasticity and signaling possibilities. Numerous alluring models of information processing and learning rules have arisen as a result of these in vitro findings, and supported by this R01, we have begun to determine which of these mechanisms are at work in awake, behaving animals. The present proposal leverages recent technical advances used and developed by the PI that enable functional imaging of calcium transients with single dendritic branch resolution and of glutamate input with synaptic scale resolution in the hippocampus of head-restrained mice performing spatial behaviors in a virtual-reality interface. Using these methods, the research proposed in this grant application will allow us to bridge two disconnected areas of neuroscience research: research characterizing the firing patterns and changes in firing patterns of hippocampal neurons during behavior, and research in reduced preparations investigating the mechanisms underlying firing and synaptic plasticity. Specifically, we aim to determine the behavioral relevance and synaptic basis of hippocampal dSpikes. This will allow testing of models of plasticity which have been developed based on in vitro data, across a wide range of parameter space, to finally establish which learning mechanisms are behaviorally relevant.

Public Health Relevance

The hippocampus is a brain structure critically involved in learning, memory and spatial navigation, and its dysfunction is associated with amnesia, Alzheimer's disease, and epilepsy. It is not known how the neurons of the hippocampus change their connections to other neurons to facilitate the learning of a new task or the memory of a specific life episode, although several candidate mechanisms have been suggested by experiments in brain slices. In the present application, we propose to establish the behavioral relevance of basic neuronal mechanisms that can be used in the brains of awake animals in order to provide a framework for understanding information processing and memory formation and retrieval in normal brain functioning and in disease states.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
2R01MH101297-06
Application #
9740006
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Ferrante, Michele
Project Start
2013-08-16
Project End
2024-01-31
Budget Start
2019-03-15
Budget End
2020-01-31
Support Year
6
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Northwestern University at Chicago
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
160079455
City
Chicago
State
IL
Country
United States
Zip Code
60611
Heys, James G; Dombeck, Daniel A (2018) Evidence for a subcircuit in medial entorhinal cortex representing elapsed time during immobility. Nat Neurosci 21:1574-1582
Radvansky, Brad A; Dombeck, Daniel A (2018) An olfactory virtual reality system for mice. Nat Commun 9:839
Sheffield, Mark E J; Adoff, Michael D; Dombeck, Daniel A (2017) Increased Prevalence of Calcium Transients across the Dendritic Arbor during Place Field Formation. Neuron 96:490-504.e5
Howe, M W; Dombeck, D A (2016) Rapid signalling in distinct dopaminergic axons during locomotion and reward. Nature 535:505-10
Sheffield, Mark E J; Dombeck, Daniel A (2015) Calcium transient prevalence across the dendritic arbour predicts place field properties. Nature 517:200-4
Heys, James G; Rangarajan, Krsna V; Dombeck, Daniel A (2014) The functional micro-organization of grid cells revealed by cellular-resolution imaging. Neuron 84:1079-90