Subiculm circuits for cortical feedback regulation of spatial mapping and learning

NIH RePORTER · NIH · R01 · $502,839 · view on reporter.nih.gov ↗

Abstract

Project Summary / Abstract Encoding of environmental location and navigational behavior in mammals involves large ensembles of specific neuron types across multiple interacting brain regions. “Place cell” and “grid cell” mapping of spatial location in the CA1 region of hippocampus and medial entorhinal cortex (EC), respectively, is thought to be fed forward to associative cortical brain regions including the posterior parietal cortex (PPC) and retrosplenial cortex (RSP) to map conjunctions of egocentric and external spatial relationships. This notion implies that the hippocampal-neocortical pathway involves a gradual transformation of spatial cognition to action along with encoding of specific route information at intermediate processing stages. While the characterization of this hippocampal feedforward output to the neocortical system has been conceptually useful for our understanding of spatial navigation processes, it is now time to consider the role of the largely unexplored “top-down” neocortical inputs from RSP to the hippocampus. The subiculum (SUB) is an under-investigated brain structure well positioned to mediate circuit interactions between the hippocampal and neocortical systems. Based on our recent discoveries, we hypothesize that specific subsets of SUB neurons receive significant direct “top-down” inputs from RSP and that these inputs yield specialized SUB encoding of multiple spatial relationships including the axis of travel, boundary vectors, and route sub-spaces. These SUB neurons are expected to overlap with the population of CA1-projecting SUB neurons that exert direct feedback regulation of hippocampus-associated spatial mapping and learning. We propose to study the synaptic circuit organization and functional implications of this “top-down” pathway from RSP cortex, to SUB, to hippocampal CA1, using recent technological advancements. To test the hypothesis, in Aim 1, we will map brain-wide circuit input connections of CA1-projecting SUB neurons and compare these to EC-projecting, and RSP-projecting SUB neurons using new viral tracing and optogenetic stimulation mapping. A combinatorial viral and genetic strategy will be used to selectively label projection-specific SUB neurons for circuit studies and physiological characterization. In Aims 2 and 3, we will link circuit connection mapping to neurophysiological function and behavior. Tetrode recordings and in vivo GCaMP6-based calcium imaging of CA1 at single-cell resolution in freely moving animals will resolve how RSP inputs and projection-specific SUB neurons modulate CA1 place cell activities and how they contribute to spatial learning and navigation. The studies will be conducted in conjunction with behavioral analyses addressing how animals learn object-place associations and routes through environments having multiple interconnected pathways. Genetically targeted neuronal inactivation will be used to establish the causality of circuit connections and function. The prop...

Key facts

NIH application ID
10318631
Project number
5R01NS104897-05
Recipient
UNIVERSITY OF CALIFORNIA-IRVINE
Principal Investigator
Douglas Arthur Nitz
Activity code
R01
Funding institute
NIH
Fiscal year
2022
Award amount
$502,839
Award type
5
Project period
2017-12-15 → 2023-11-30