A fundamental aspect of our existence is the fact that we move through space. We do not do so randomly; rather, we use a variety of different strategies to reach our navigational goals efficiently. One such strategy is landmark-based navigation (LBN), which is the use of stable landmarks to determine one's location and orientation relative to the enduring spatial structure of the world. The current application describes a competing renewal of a research program in which we use functional magnetic resonance imaging (fMRI), transcranial magnetic stimulation (TMS), and cognitive behavioral testing to understand the neural systems that underlie LBN. Under the theoretical scheme we have developed, LBN involves three cognitive mechanisms: a landmark recognition mechanism, a localization/orientation mechanism, and a route planning mechanism. During the initial funding period, we used multivoxel pattern analysis (MVPA) of fMRI data to demonstrate that the parahippocampal place area (PPA) supports landmark recognition and the retrosplenial complex (RSC) supports localization/orientation. These results indicate that the neural network involved in LBN can be fractionated into functional subsystems tied to the three cognitive mechanisms. Our goals in the next funding period are to use these discoveries as a springboard to understand the mechanistic operation of the LBN system and to extend the investigation to encompass route planning.
Aim 1 is to delineate the information processing functions of the landmark recognition mechanism in the PPA and to identify its functional inputs.
Aim 2 is to understand the how the RSC uses external features and egocentric experience to mediate localization/orientation.
Aim 3 is to identify and characterize the neural mechanisms that support route planning in RSC and the medial temporal lobe (MTL). If successful, this research will result in a detailed theory of the neural basis of landmark-based navigation. This knowledge will have important health implications in two domains. First, understanding the mechanisms that underlie LBN is critical for the development of rehabilitation strategies and navigational aids for the blind. Second, because the brain regions investigated are often impacted early in neurodegenerative diseases such as Alzheimer's dementia, the knowledge gained about these systems will be useful for diagnosing and managing these diseases.

Public Health Relevance

This project examines the neural mechanisms underlying landmark-based spatial navigation. This knowledge is important for developing rehabilitation strategies in people with impaired sight, who often suffer from way finding difficulties. Moreover, because the brain regions that support spatial navigation are typically impacted early in neurodegenerative diseases such as Alzheimer's dementia, knowledge about these systems is important for developing strategies for diagnosing and managing these diseases.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY022350-07
Application #
9767784
Study Section
Cognition and Perception Study Section (CP)
Program Officer
Flanders, Martha C
Project Start
2013-03-01
Project End
2020-08-31
Budget Start
2019-09-01
Budget End
2020-08-31
Support Year
7
Fiscal Year
2019
Total Cost
Indirect Cost
Name
University of Pennsylvania
Department
Psychology
Type
Schools of Arts and Sciences
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
Julian, Joshua B; Kamps, Frederik S; Epstein, Russell A et al. (2018) Dissociable spatial memory systems revealed by typical and atypical human development. Dev Sci :e12737
Julian, Joshua B; Keinath, Alexandra T; Frazzetta, Giulia et al. (2018) Human entorhinal cortex represents visual space using a boundary-anchored grid. Nat Neurosci 21:191-194
Keinath, Alexandra T; Epstein, Russell A; Balasubramanian, Vijay (2018) Environmental deformations dynamically shift the grid cell spatial metric. Elife 7:
Bonner, Michael F; Epstein, Russell A (2018) Computational mechanisms underlying cortical responses to the affordance properties of visual scenes. PLoS Comput Biol 14:e1006111
Julian, Joshua B; Keinath, Alexandra T; Marchette, Steven A et al. (2018) The Neurocognitive Basis of Spatial Reorientation. Curr Biol 28:R1059-R1073
Vass, Lindsay K; Epstein, Russell A (2017) Common Neural Representations for Visually Guided Reorientation and Spatial Imagery. Cereb Cortex 27:1457-1471
Bonner, Michael F; Epstein, Russell A (2017) Coding of navigational affordances in the human visual system. Proc Natl Acad Sci U S A 114:4793-4798
Keinath, Alex T; Julian, Joshua B; Epstein, Russell A et al. (2017) Environmental Geometry Aligns the Hippocampal Map during Spatial Reorientation. Curr Biol 27:309-317
Marchette, Steven A; Ryan, Jack; Epstein, Russell A (2017) Schematic representations of local environmental space guide goal-directed navigation. Cognition 158:68-80
Epstein, Russell A; Patai, Eva Zita; Julian, Joshua B et al. (2017) The cognitive map in humans: spatial navigation and beyond. Nat Neurosci 20:1504-1513

Showing the most recent 10 out of 17 publications