Egocentric and allocentric representations of space in the rodent brain
Open accessAbstract
Spatial signals are prevalent within the hippocampus and its neighboring regions. It is generally accepted that these signals are defined with respect to the external world (i.e., a world-centered, or allocentric, frame of reference). Recently, evidence of egocentric processing (i.e., self-centered, defined relative to the subject) in the extended hippocampal system has accumulated. These results support the idea that egocentric sensory information, derived from primary sensory cortical areas, may be transformed to allocentric representations that interact with the allocentric hippocampal system. We propose a framework to explain the implications of the egocentric-allocentric transformations to the functions of the medial temporal lobe memory system.
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Egocentric spatial representations are found mostly in regions upstream of the hippocampal-entorhinal allocentric representations, with some overlaps (Wang et al., 2020).
“Egocentric spatial representations are found mostly in regions upstream of the hippocampal–entorhinal allocentric representations (e.g., primary sensory cortex), with some overlaps (e.g. in the hippocampus and lateral entorhinal cortex) (Wang et al., 2020).”
From Does viewing a top-down map facilitate spatial learning from navigation in a virtual environment? (2026) · cites this paper as Wang et al., 2020
Many vectorial codes exist in mammalian navigation systems, including some in body-centric coordinates and others in world-centric coordinates.
“More generally, there are many vectorial codes in mammalian navigation systems1,2, including some in body-centric coordinates34,35, and others in world-centric coordinates34,36–38.”
From Transforming representations of movement from body- to world-centric space (2022) · cites this paper as [2]
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Cites
(1978) · UA Campus Repository (The University of Arizona) · Cited by 8,010 · see citing works
The hippocampus as a cognitive map
Passingham, R. E. (1979) · Neuroscience · doi:10.1016/0306-4522(79)90015-0 · Cited by 5,128 · see citing works
Microstructure of a spatial map in the entorhinal cortex
Hafting, T., Fyhn, M., Molden, S., Moser, M.-B., & Moser, E. I. (2005) · Nature · doi:10.1038/nature03721 · Cited by 4,068 · see citing works
(1995) · Choice Reviews Online · doi:10.5860/choice.32-5931 · Cited by 2,337 · see citing works
Taube, J., Muller, R., & Ranck, J. (1990) · The Journal of Neuroscience · doi:10.1523/jneurosci.10-02-00420.1990 · Cited by 1,809 · see citing works
What does the retrosplenial cortex do?
Vann, S. D., Aggleton, J. P., & Maguire, E. A. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2733 · Cited by 1,409 · see citing works
Intentional Maps in Posterior Parietal Cortex
Andersen, R. A., & Buneo, C. A. (2002) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.25.112701.142922 · Cited by 1,294 · see citing works
Remembering the past and imagining the future: A neural model of spatial memory and imagery.
Byrne, P., Becker, S., & Burgess, N. (2007) · Psychological Review · doi:10.1037/0033-295x.114.2.340 · Cited by 1,011 · see citing works
Organizing conceptual knowledge in humans with a gridlike code
Constantinescu, A. O., O’Reilly, J. X., & Behrens, T. E. J. (2016) · Science · doi:10.1126/science.aaf0941 · Cited by 937 · see citing works
Hippocampal remapping and grid realignment in entorhinal cortex
Fyhn, M., Hafting, T., Treves, A., Moser, M.-B., & Moser, E. I. (2007) · Nature · doi:10.1038/nature05601 · Cited by 749 · see citing works
Vector-based navigation using grid-like representations in artificial agents
Banino, A., Barry, C., Uría, B., Blundell, C., Lillicrap, T., Mirowski, P., Pritzel, A., Chadwick, M. J., Degris, T., Modayil, J., et al. (2018) · Nature · doi:10.1038/s41586-018-0102-6 · Cited by 682 · see citing works
Allocentric and Egocentric Spatial Representations: Definitions, Distinctions, and Interconnections
Klatzky, R. L. (1998) · Lecture Notes in Computer Science · doi:10.1007/3-540-69342-4_1 · Cited by 664 · see citing works
Knierim, J. J., Neunuebel, J. P., & Deshmukh, S. S. (2014) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2013.0369 · Cited by 425 · see citing works
Self-citationHead direction, place, and movement correlates for cells in the rat retrosplenial cortex.
Cho, J., & Sharp, P. E. (2001) · Behavioral Neuroscience · doi:10.1037/0735-7044.115.1.3 · Cited by 385 · see citing works
Makin, T. R., Holmes, N. P., & Zohary, E. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.3653-06.2007 · Cited by 381 · see citing works
Beyond the Cognitive Map: From Place Cells to Episodic Memory
Redish, A. D. (1999) · Cited by 369 · see citing works
Object-vector coding in the medial entorhinal cortex
Høydal, Ø. A., Skytøen, E. R., Andersson, S. O., Moser, M.-B., & Moser, E. I. (2019) · Nature · doi:10.1038/s41586-019-1077-7 · Cited by 366 · see citing works
Vectorial representation of spatial goals in the hippocampus of bats
Sarel, A., Finkelstein, A., Las, L., & Ulanovsky, N. (2017) · Science · doi:10.1126/science.aak9589 · Cited by 340 · see citing works
Using Grid Cells for Navigation
Bush, D., Barry, C., Manson, D., & Burgess, N. (2015) · Neuron · doi:10.1016/j.neuron.2015.07.006 · Cited by 329 · see citing works
Retrosplenial cortex maps the conjunction of internal and external spaces
Alexander, A. S., & Nitz, D. A. (2015) · Nature Neuroscience · doi:10.1038/nn.4058 · Cited by 299 · see citing works
Social place-cells in the bat hippocampus
Omer, D. B., Maimon, S. R., Las, L., & Ulanovsky, N. (2018) · Science · doi:10.1126/science.aao3474 · Cited by 280 · see citing works
Egocentric coding of external items in the lateral entorhinal cortex
Wang, C., Chen, X., Lee, H., Deshmukh, S. S., Yoganarasimha, D., Savelli, F., & Knierim, J. J. (2018) · Science · doi:10.1126/science.aau4940 · Cited by 276 · see citing works
Self-citationSpatial representations of self and other in the hippocampus
Danjo, T., Toyoizumi, T., & Fujisawa, S. (2018) · Science · doi:10.1126/science.aao3898 · Cited by 257 · see citing works
McNaughton, B. L., Leonard, B. W., & Chen, L. (1989) · Psychobiology · doi:10.1007/bf03337774 · Cited by 244 · see citing works
Wiener, S. I. (1993) · Journal of Neuroscience · doi:10.1523/jneurosci.13-09-03802.1993 · Cited by 233 · see citing works
A neural-level model of spatial memory and imagery
Bicanski, A., & Burgess, N. (2018) · eLife · doi:10.7554/elife.33752 · Cited by 230 · see citing works
Influence of local objects on hippocampal representations: Landmark vectors and memory
Deshmukh, S. S., & Knierim, J. J. (2013) · Hippocampus · doi:10.1002/hipo.22101 · Cited by 217 · see citing works
Self-citationInteraction of Egocentric and World-Centered Reference Frames in the Rat Posterior Parietal Cortex
Wilber, A. A., Clark, B. J., Forster, T. C., Tatsuno, M., & McNaughton, B. L. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.0511-14.2014 · Cited by 200 · see citing works
Egocentric boundary vector tuning of the retrosplenial cortex
Alexander, A. S., Carstensen, L. C., Hinman, J. R., Raudies, F., Chapman, G. W., & Hasselmo, M. E. (2020) · Science Advances · doi:10.1126/sciadv.aaz2322 · Cited by 197 · see citing works
Causal Influence of Visual Cues on Hippocampal Directional Selectivity
Acharya, L., Aghajan, Z. M., Vuong, C., Moore, J. J., & Mehta, M. R. (2016) · Cell · doi:10.1016/j.cell.2015.12.015 · Cited by 196 · see citing works
Nilssen, E. S., Doan, T. P., Nigro, M. J., Ohara, S., & Witter, M. P. (2019) · Hippocampus · doi:10.1002/hipo.23145 · Cited by 178 · see citing works
An allocentric spatial model for the hippocampal cognitive map
O'Keefe, J. M. (1991) · Hippocampus · doi:10.1002/hipo.450010303 · Cited by 162 · see citing works
Knierim, J. J., & Hamilton, D. A. (2011) · Physiological Reviews · doi:10.1152/physrev.00021.2010 · Cited by 148 · see citing works
Self-citationMeyer, A. F., Poort, J., O'Keefe, J. M., Sahani, M., & Linden, J. F. (2018) · Neuron · doi:10.1016/j.neuron.2018.09.020 · Cited by 145 · see citing works
Lateral entorhinal cortex is necessary for associative but not nonassociative recognition memory
Wilson, D. I. G., Watanabe, S., Milner, H., & Ainge, J. A. (2013) · Hippocampus · doi:10.1002/hipo.22165 · Cited by 137 · see citing works
Computer simulation of hippocampal place cells
Sharp, P. E. (1991) · Psychobiology · doi:10.3758/bf03327179 · Cited by 131 · see citing works
A sense of space in postrhinal cortex
LaChance, P. A., Todd, T. P., & Taube, J. S. (2019) · Science · doi:10.1126/science.aax4192 · Cited by 129 · see citing works
Pyapali, G. K., Attila Gabor, S. I. K., Penttonen, M., Buzsáki, G., & Turner, D. A. (1998) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19980216)391:3 · Cited by 128 · see citing works
Encoding of Head Direction by Hippocampal Place Cells in Bats
Rubin, A., Yartsev, M. M., & Ulanovsky, N. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.5393-12.2014 · Cited by 124 · see citing works
Efficient cortical coding of 3D posture in freely behaving rats
Mimica, B., Dunn, B. A., Tombaz, T., Bojja, V. P. T. N. C. S., & Whitlock, J. R. (2018) · Science · doi:10.1126/science.aau2013 · Cited by 124 · see citing works
Neuronal representation of environmental boundaries in egocentric coordinates
Hinman, J. R., Chapman, G. W., & Hasselmo, M. E. (2019) · Nature Communications · doi:10.1038/s41467-019-10722-y · Cited by 112 · see citing works
Savelli, F., & Knierim, J. J. (2019) · Journal of Experimental Biology · doi:10.1242/jeb.188912 · Cited by 93 · see citing works
Self-citationGofman, X., Tocker, G., Weiss, S., Boccara, C. N., Lu, L., Moser, M., Moser, E. I., Morris, G., & Derdikman, D. (2019) · Current Biology · doi:10.1016/j.cub.2019.07.007 · Cited by 93 · see citing works
Transformation of the head-direction signal into a spatial code
Peyrache, A., Schieferstein, N., & Buzsáki, G. (2017) · Nature Communications · doi:10.1038/s41467-017-01908-3 · Cited by 83 · see citing works
Navratilova, Z., Hoang, L. T., Schwindel, C. D., Tatsuno, M., & McNaughton, B. L. (2012) · Frontiers in Neural Circuits · doi:10.3389/fncir.2012.00006 · Cited by 78 · see citing works
Heading direction with respect to a reference point modulates place-cell activity
Jercog, P. E., Ahmadian, Y., Woodruff, C. M., Deb-Sen, R., Abbott, L. F., & Kandel, E. R. (2019) · Nature Communications · doi:10.1038/s41467-019-10139-7 · Cited by 77 · see citing works
Head direction is coded more strongly than movement direction in a population of entorhinal neurons
Raudies, F., Brandon, M. P., Chapman, G. W., & Hasselmo, M. E. (2014) · Brain Research · doi:10.1016/j.brainres.2014.10.053 · Cited by 72 · see citing works
Coordinating different representations in the hippocampus
Kelemen, E., & Fenton, A. A. (2015) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2015.12.011 · Cited by 68 · see citing works
Lisman, J. E. (2007) · Progress in brain research · doi:10.1016/s0079-6123(07)63033-7 · Cited by 67 · see citing works
Parahippocampal and retrosplenial connections of rat posterior parietal cortex
Olsen, G. M., Ohara, S., Iijima, T., & Witter, M. P. (2016) · Hippocampus · doi:10.1002/hipo.22701 · Cited by 66 · see citing works
Egocentric boundary vector tuning of the retrosplenial cortexPreprint
Alexander, A. S., Carstensen, L. C., Hinman, J. R., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/702712 · Cited by 37 · see citing works
Multiplexed code of navigation variables in anterior limbic areasPreprint
Laurens, J., Abrego, A., Cham, H., Popeney, B., Yu, Y., Rotem, N., Aarse, J., Asprodini, E. K., Dickman, J. D., & Angelaki, D. E. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/684464 · Cited by 14 · see citing works
Cortico-hippocampal communication by way of parallel parahippocampal-subicular pathways.
Lavenex (2000) · Pure Amsterdam UMC · doi:10.1002/1098-1063(2000)10:4 · Cited by 1 · see citing works
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“Egocentric spatial representations are found mostly in regions upstream of the hippocampal–entorhinal allo-centric representations (e.g., primary sensory cortex), with some overlaps (e.g. in the hippocampus and lateral entorhinal cortex) (Wang et al., 2020).”
- Authors
- Wang, C., Chen, X., & Knierim, J. J.
- Affiliations
- Johns Hopkins University (US)
- Corresponding author
- Wang, Cheng
- Knierim, James J
- Venue
- Current Opinion in Neurobiology
- Publisher
- Elsevier BV
- Published
- 2020-02
- Volume
- 60
- Pages
- 12-20
- ISSN
- 0959-4388 (ISSN-L)
- PMC
- PMC7080648
- OpenAlex
- W2990041000
- Cited by
- 141
- References
- 53
- Citations by year
- 2026: 17 · 2025: 24 · 2024: 22 · 2023: 26 · 2022: 16 · 2021: 20 · 2020: 16
- FWCI
- 1.65
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- Current Opinion in Neurobiology (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health
- 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
- egocentric spatial representation, allocentric spatial representation, hippocampus, lateral entorhinal cortex, episodic memory, rodent brain, spatial coding, reference frames
- MeSH terms
- Animals, Hippocampus, Memory, Rodentia, Space Perception
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