The DOI matches its Crossref record; 37 of the 37 references it cites were found in a registry or an index.
Social place-cells in the bat hippocampus
Abstract
The representation of others in space: Different sets of neurons encode the spatial position and orientation of an organism. However, social animals need to know the position of other individuals for social interactions, observational learning, and group navigation. Surprisingly, very little is known about how the position of other animals is represented in the brain. Danjo et al. and Omer et al. now report the discovery of a subgroup of neurons in hippocampal area CA1 that encodes the presence of conspecifics in rat and bat brains, respectively. Science , this issue p. 213 , p. 218
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“Prior investigations in rodents and primates, for example, have provided evidence for the presence of neurons that encode information about other individuals, demonstrating changes in activity when the animals observe another’s appetitive or aversive experiences 1–11.”
From Reduced sociability and social agency encoding in adult Shank3-mutant mice are restored through gene re-expression in real time (2021) · cites this paper as [6]
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“Previous investigations have provided insight into how discrete aspects of another animal’s experience, such as receipt of reward, may be encoded by cells 1–7,9.”
From Reduced sociability and social agency encoding in adult Shank3-mutant mice are restored through gene re-expression in real time (2021) · cites this paper as [6]
Citations
Cites
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
Dynamics of the Hippocampal Ensemble Code for Space
Wilson, M. A., & McNaughton, B. L. (1993) · Science · doi:10.1126/science.8351520 · Cited by 2,350
Taube, J., Muller, R., & Ranck, J. (1990) · The Journal of Neuroscience · doi:10.1523/jneurosci.10-02-00420.1990 · Cited by 1,809
Reverse replay of behavioural sequences in hippocampal place cells during the awake state
Foster, D. J., & Wilson, M. A. (2006) · Nature · doi:10.1038/nature04587 · Cited by 1,727
Three-axis attitude determination from vector observations
SHUSTER, M. D., & OH, S. D. (1981) · Journal of Guidance and Control · doi:10.2514/3.19717 · Cited by 1,399
Memory of sequential experience in the hippocampus during slow wave sleep
Lee, A. K., & Wilson, M. A. (2002) · Neuron · doi:10.1016/s0896-6273(02)01096-6 · Cited by 1,296
Hippocampal place-cell sequences depict future paths to remembered goals
Pfeiffer, B. E., & Foster, D. J. (2013) · Nature · doi:10.1038/nature12112 · Cited by 1,216
Representation of Geometric Borders in the Entorhinal Cortex
Solstad, T., Boccara, C. N., Kropff, E., Moser, M.-B., & Moser, E. I. (2008) · Science · doi:10.1126/science.1166466 · Cited by 1,213
Forward and reverse hippocampal place-cell sequences during ripples
Diba, K., & Buzsáki, G. (2007) · Nature Neuroscience · doi:10.1038/nn1961 · Cited by 1,205
The hippocampal CA2 region is essential for social memory
Hitti, F. L., & Siegelbaum, S. A. (2014) · Nature · doi:10.1038/nature13028 · Cited by 976
Hippocampal replay of extended experience
Davidson, T. J., Kloosterman, F., & Wilson, M. A. (2009) · Neuron · doi:10.1016/j.neuron.2009.07.027 · Cited by 806
Boundary Vector Cells in the Subiculum of the Hippocampal Formation
Lever, C., Burton, S., Jeewajee, A., O'Keefe, J., & Burgess, N. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.1319-09.2009 · Cited by 753
Preplay of future place cell sequences by hippocampal cellular assemblies
Dragoi, G., & Tonegawa, S. (2011) · Nature · doi:10.1038/nature09633 · Cited by 716
Markus, E. J., Qin, Y., Leonard, B. W., Skaggs, W. E., McNaughton, B. L., & Barnes, C. A. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-11-07079.1995 · Cited by 698
Ventral CA1 neurons store social memory
Okuyama, T., Kitamura, T., Roy, D. S., Itohara, S., & Tonegawa, S. (2016) · Science · doi:10.1126/science.aaf7003 · Cited by 657
Can We Reconcile the Declarative Memory and Spatial Navigation Views on Hippocampal Function?
Eichenbaum, H., & Cohen, N. J. (2014) · Neuron · doi:10.1016/j.neuron.2014.07.032 · Cited by 654
Prospective and Retrospective Memory Coding in the Hippocampus
Ferbinteanu, J., & Shapiro, M. L. (2003) · Neuron · doi:10.1016/s0896-6273(03)00752-9 · Cited by 560
Experience-dependent rescaling of entorhinal grids
Barry, C., Hayman, R. M. A., Burgess, N., & Jeffery, K. J. (2007) · Nature Neuroscience · doi:10.1038/nn1905 · Cited by 545
The mirror mechanism: a basic principle of brain function
Rizzolatti, G., & Sinigaglia, C. (2016) · Nature reviews. Neuroscience · doi:10.1038/nrn.2016.135 · Cited by 521
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
Representation of Three-Dimensional Space in the Hippocampus of Flying Bats
Yartsev, M. M., & Ulanovsky, N. (2013) · Science · doi:10.1126/science.1235338 · Cited by 416
Self-citationGrid cells without theta oscillations in the entorhinal cortex of bats
Yartsev, M. M., Witter, M. P., & Ulanovsky, N. (2011) · Nature · doi:10.1038/nature10583 · Cited by 401
Self-citationInfluence of boundary removal on the spatial representations of the medial entorhinal cortex
Savelli, F., Yoganarasimha, D., & Knierim, J. J. (2008) · Hippocampus · doi:10.1002/hipo.20511 · Cited by 363
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 345
Self-citationRediscovering area CA2: unique properties and functions
Dudek, S. M., Alexander, G. M., & Farris, S. (2016) · Nature reviews. Neuroscience · doi:10.1038/nrn.2015.22 · Cited by 333
Xiaoping, Y., Bachmann, E. R., & McGhee, R. B. (2008) · IEEE Transactions on Instrumentation and Measurement · doi:10.1109/tim.2007.911646 · Cited by 321
Moita, M. A. P., Rosis, S., Zhou, Y., LeDoux, J. E., & Blair, H. T. (2003) · Neuron · doi:10.1016/s0896-6273(03)00033-3 · Cited by 295
Traces of experience in the lateral entorhinal cortex
Tsao, A., Moser, M.-B., & Moser, E. I. (2013) · Current Biology · doi:10.1016/j.cub.2013.01.036 · Cited by 290
Three-dimensional head-direction coding in the bat brain
Finkelstein, A., Derdikman, D., Rubin, A., Foerster, J., Las, L., & Ulanovsky, N. (2014) · Nature · doi:10.1038/nature14031 · Cited by 286
Self-citationHippocampal cellular and network activity in freely moving echolocating bats
Ulanovsky, N., & Moss, C. F. (2007) · Nature Neuroscience · doi:10.1038/nn1829 · Cited by 283
Self-citationInternally organized mechanisms of the head direction sense
Peyrache, A., Lacroix, M. M., Petersen, P. C., & Buzsáki, G. (2015) · Nature Neuroscience · doi:10.1038/nn.3968 · Cited by 274
Spatial Representation along the Proximodistal Axis of CA1
Henriksen, E. J., Colgin, L. L., Barnes, C. A., Witter, M. P., Moser, M., & Moser, E. I. (2010) · Neuron · doi:10.1016/j.neuron.2010.08.042 · Cited by 273
Autoassociative dynamics in the generation of sequences of hippocampal place cells
Pfeiffer, B. E., & Foster, D. J. (2015) · Science · doi:10.1126/science.aaa9633 · Cited by 176
Weak and Nondiscriminative Responses to Conspecifics in the Rat Hippocampus
von Heimendahl, M., Rao, R. P., & Brecht, M. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.3812-11.2012 · Cited by 66
Social observation enhances cross-environment activation of hippocampal place cell patterns
Mou, X., & Ji, D. (2016) · eLife · doi:10.7554/elife.18022 · Cited by 31
Hippocampal place cell activity during chasing of a moving object associated with reward in rats
Ho, S. A., Hori, E., Kobayashi, T., Umeno, K., Tran, A. H., Ono, T., & Nishijo, H. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.09.004 · Cited by 27
Zynyuk, L., Huxter, J. R., Muller, R. U., & Fox, S. E. (2011) · Hippocampus · doi:10.1002/hipo.20977 · Cited by 24
Flagged first, then by citations
Research works printed but not linked: 3
- J. O’Keefe L. Nadel The Hippocampus as a Cognitive Map (Oxford Univ. Press 1978).
- G. Neuweiler The Biology of Bats (Oxford Univ. Press 2000).
- W. E. Skaggs B. L. McNaughton M. A. Wilson E. J. Markus in Advances in Neural Information Processing Systems 5 S. J. Hanson J. D. Cowan C. L. Giles Eds. (Morgan Kaufman 1993) pp. 1030–1037.
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Behrens, T. E. J., Muller, T. H., Whittington, J. C. R., Mark, S., Baram, A. B., Stachenfeld, K. L., & Kurth-Nelson, Z. (2018) · Neuron · doi:10.1016/j.neuron.2018.10.002 · Cited by 1,055
Navigating cognition: Spatial codes for human thinking
Bellmund, J. L. S., Gärdenfors, P., Moser, E. I., & Doeller, C. F. (2018) · Science · doi:10.1126/science.aat6766 · Cited by 643
Buzsáki, G. (2019) · doi:10.1093/oso/9780190905385.001.0001 · Cited by 383
Mirror neurons 30 years later: implications and applications
Bonini, L., Rotunno, C., Arcuri, E., & Gallese, V. (2022) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2022.06.003 · Cited by 373
Targeted Activation of Hippocampal Place Cells Drives Memory-Guided Spatial Behavior
Robinson, N. T. M., Descamps, L. A. L., Russell, L. E., Buchholz, M. O., Bicknell, B. A., Antonov, G. K., Lau, J. Y. N., Nutbrown, R., Schmidt-Hieber, C., & Häusser, M. (2020) · Cell · doi:10.1016/j.cell.2020.09.061 · Cited by 281
Metadata
- Authors
- Omer, D. B., Maimon, S. R., Las, L., & Ulanovsky, N.
- Affiliations
- Weizmann Institute of Science (IL)
- Corresponding author
- Las, Liora
- Ulanovsky, Nachum
- Venue
- Science
- Published
- 2018-01-12
- Volume
- 359
- Issue
- 6372
- Pages
- 218-224
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- OpenAlex
- W2782639658
- Cited by
- 280
- References
- 37
- Citations by year
- 2026: 18 · 2025: 49 · 2024: 32 · 2023: 48 · 2022: 22 · 2021: 23 · 2020: 32 · 2019: 36 · 2018: 20
- FWCI
- 16.53
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- Funders
- European Research Council (NATURAL_BAT_NAV)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Spatial Cognition and Navigation
- Life Sciences › Agricultural and Biological Sciences › Ecology, Evolution, Behavior and Systematics › Bat Biology and Ecology Studies
- Keywords
- hippocampus, dorsal CA1, bats, observational learning, allocentric spatial representation, trajectory planning
- MeSH terms
- Place Cells, Action Potentials, Animals, Chiroptera, Flight, Animal, Male, Neurons, Space Perception, Spatial Behavior, CA1 Region, Hippocampal, Spatial Learning
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