The Boundary Vector Cell Model of Place Cell Firing and Spatial Memory
Open accessAbstract
We review evidence for the boundary vector cell model of the environmental determinants of the firing of hippocampal place cells. Preliminary experimental results are presented concerning the effects of addition or removal of environmental boundaries on place cell firing and evidence that boundary vector cells may exist in the subiculum. We review and update computational simulations predicting the location of human search within a virtual environment of variable geometry, assuming that boundary vector cells provide one of the input representations of location used in mammalian spatial memory. Finally, we extend the model to include experience-dependent modification of connection strengths through a BCM-like learning rule - the size and sign of strength change is influenced by historic activity of the postsynaptic cell. Simulations are compared to experimental data on the firing of place cells under geometrical manipulations to their environment. The relationship between neurophysiological results in rats and spatial behaviour in humans is discussed.
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A purely geometric model like the boundary vector model does not offer an explanation for the direction sensitivity of place field remapping.
“In contrast, a purely geometric model like the boundary vector model (41) does not offer an explanation for the direction sensitivity of place field remapping.”
From Space is a latent sequence: A theory of the hippocampus (2024) · cites this paper as [41]
The Learning section (page unavailable) says nonparametric remapping remains to be understood, and the Conclusion (page unavailable) questions whether the current feed-forward BVC model can explain rapid, coherent remapping. These passages support a limitation concerning remapping generally, but they do not address the claimed direction sensitivity of remapping. (LLM, conf=0.78)
Experimental — accuracy not yet measuredThe BVC model predicts a duplication of place fields in S2.
“Crucially, the BVC model predicts a duplication of PFs in S2.”
From A population code for spatial representation in the zebrafish telencephalon (2024) · cites this paper as [34]
The “Inserting barriers” section says the BVC model predicts doubled place fields after an extended barrier is added, particularly for some fields near a wall. Our copy does not identify an S2 condition, so it supports the duplication prediction but not its specific application to S2. (LLM, conf=0.82)
Experimental — accuracy not yet measuredCSCGs can transfer prior knowledge to new environments and infer shortcut paths through unobserved locations by treating the learned transition graph as a schema and learning just the emission matrix.
“CSCGs can also transfer prior knowledge to new environments and infer shortcut paths through unobserved locations by treating the learned transition graph as a schema (40–42) and learning just the emission matrix.”
From Space is a latent sequence: A theory of the hippocampus (2024) · cites this paper as [41]
The BVC-based models of behaviour section describes navigation using stored boundary-vector-cell activity, and the Conclusion discusses learned connections between BVCs and place cells. Neither passage addresses reusing a learned transition graph as a schema, inferring shortcuts through unobserved locations, or learning only an emission matrix. Searches for those terms and for transfer to new environments found no supporting passage; page numbers were not available in our copy. (LLM, conf=0.75)
Experimental — accuracy not yet measured
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Object-vector coding in the medial entorhinal cortex
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Grid cells and cortical representation
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Structuring knowledge with cognitive maps and cognitive graphs
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The Cognitive Architecture of Spatial Navigation: Hippocampal and Striatal Contributions
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A neural-level model of spatial memory and imagery
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Self-citationGrid cells and theta as oscillatory interference: Electrophysiological data from freely moving rats
Jeewajee, A., Barry, C., O'Keefe, J., & Burgess, N. (2008) · Hippocampus · doi:10.1002/hipo.20510 · Cited by 212 · see citing works
Self-citationRetrosplenial cortex codes for permanent landmarks
Auger, S. D., Mullally, S. L., & Maguire, E. A. (2012) · PLoS ONE · doi:10.1371/journal.pone.0043620 · Cited by 205 · see citing works
Neuronal vector coding in spatial cognition
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Spatial goal coding in the hippocampal formation
Nyberg, N., Duvelle, É., Barry, C., & Spiers, H. J. (2022) · Neuron · doi:10.1016/j.neuron.2021.12.012 · Cited by 141 · see citing works
Self-citationKnierim, J. J., & Hamilton, D. A. (2011) · Physiological Reviews · doi:10.1152/physrev.00021.2010 · Cited by 148 · see citing works
George, D., Rikhye, R. V., Gothoskar, N., Guntupalli, J. S., Dedieu, A., & Lázaro-Gredilla, M. (2021) · Nature Communications · doi:10.1038/s41467-021-22559-5 · Cited by 109 · see citing works
Savelli, F., & Knierim, J. J. (2019) · Journal of Experimental Biology · doi:10.1242/jeb.188912 · Cited by 93 · see citing works
The place-cell representation of volumetric space in rats
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Self-citationEnvironmental deformations dynamically shift the grid cell spatial metric
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Impaired allocentric spatial memory underlying topographical disorientation
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Place field repetition and spatial learning in a multicompartment environment
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Thalamocortical interactions in cognition and disease: The mediodorsal and anterior thalamic nuclei
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Hippocampal place cells encode global location but not connectivity in a complex space
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Self-citationA model of egocentric to allocentric understanding in mammalian brains
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Self-citationSchematic representations of local environmental space guide goal-directed navigation
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Self-citationA stable hippocampal representation of a space requires its direct experience
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A population code for spatial representation in the zebrafish telencephalon
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“To search for cells whose firing properties follow the BVC model 34 we fitted a BVC model (see below) to candidate neurons in the telencephalon.”
Boundary vector cells in the goldfish central telencephalon encode spatial information
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Space is a latent sequence: A theory of the hippocampus
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Predictive Representations: Building Blocks of Intelligence
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Self-citation“A compressed representation of spatial distance in the rodent hippocampus’’
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Enhancing spatial navigation performance through boundary cues in the virtual environment
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- Authors
- Barry, C., Lever, C., Hayman, R., Hartley, T., Burton, S., O'Keefe, J., Jeffery, K., & Burgess, Ν.
- Affiliations
- University College London (GB)
- Venue
- Reviews in the Neurosciences
- Publisher
- Walter de Gruyter GmbH
- Published
- 2006-01
- Volume
- 17
- Issue
- 1-2
- Pages
- 71-97
- ISSN
- 0334-1763 (ISSN-L)
- 2191-0200
- PMC
- PMC2677716
- OpenAlex
- W1968533788
- Cited by
- 401
- References
- 96
- Citations by year
- 2026: 13 · 2025: 28 · 2024: 35 · 2023: 24 · 2022: 21 · 2021: 27 · 2020: 23 · 2019: 27 · 2018: 29 · 2017: 27 · 2016: 22 · 2015: 15 · 2014: 20 · 2013: 20 · 2012: 15
- FWCI
- 5.50
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- Reviews in the Neurosciences (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- ENLIGHTEN (Jurnal Bimbingan dan Konseling Islam) (submittedVersion)
- UCL Discovery (University College London) (submittedVersion)
- Funders
- Wellcome Trust (071248, 76328)
- Biotechnology and Biological Sciences Research Council (BBS/B/1566X)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Physical Sciences › Engineering › Automotive Engineering › Spatial Cognition and Navigation
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Keywords
- place cells, hippocampus, spatial memory, environmental boundaries, subiculum, virtual navigation, Hebbian learning, spatial representation, rats
- MeSH terms
- Action Potentials, Animals, Hippocampus, Humans, Learning, Memory, Models, Neurological, Neural Pathways, Neuronal Plasticity, Neurons, Orientation, Space Perception, Rats
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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