Cited by 1,193Memory and Neural MechanismsMemory Processes and InfluencesNeurogenesis and neuroplasticity mechanisms

Hippocampal ‘time cells’ bridge the gap in memory for discontiguous events

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MacDonald, Christopher J., Lepage, Kyle Q., Eden, Uri T., Eichenbaum, Howard·2011·Neuron

Abstract

The hippocampus is critical to remembering the flow of events in distinct experiences and, in doing so, bridges temporal gaps between discontiguous events. Here, we report a robust hippocampal representation of sequence memories, highlighted by "time cells" that encode successive moments during an empty temporal gap between the key events, while also encoding location and ongoing behavior. Furthermore, just as most place cells "remap" when a salient spatial cue is altered, most time cells form qualitatively different representations ("retime") when the main temporal parameter is altered. Hippocampal neurons also differentially encode the key events and disambiguate different event sequences to compose unique, temporally organized representations of specific experiences. These findings suggest that hippocampal neural ensembles segment temporally organized memories much the same as they represent locations of important events in spatially defined environments.

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Crossref · 10.1016/j.neuron.2011.07.012

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  • The hippocampal pallium of teleost fish is critical for the temporal dimension of associative memories required for trace classical conditioning.

    “These deficits are strikingly similar to those reported in hippocampal-lesioned mammals [216,226,227,228,229,230,231], and reveal that the hippocampal pallium of teleost fish is critical for the temporal dimension of the associative memories required for trace classical conditioning.”

    From Spatial Cognition in Teleost Fish: Strategies and Mechanisms (2021) · cites this paper as [227]

  • Hippocampal time cells exhibit gradually changing activity over seconds during unfilled delays even when the animal remains in a fixed location, which is consistent with drift.

    “Hippocampal “time cells” show gradually changing activity patterns on the order of seconds during unfilled delays even when the animal’s location is fixed [6–9], consistent with drift.”

    From Does mental context drift or shift? (2017) · cites this paper as [7]

  • Place cell activity in rats can encode information about the 'what' and 'when' of events.

    “evidence suggests that place cell activity in rats can also encode information about the ‘what’ (e.g. odours and their status, i.e. match/non-match [124–126]) and ‘when’ (i.e. elapsed time [127,128]) of events.”

    From Is episodic-like memory <i>like</i> episodic memory? (2024) · cites this paper as [128]

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Authors
MacDonald, C. J., Lepage, K. Q., Eden, U. T., & Eichenbaum, H.
Affiliations
Boston University (US)
Corresponding author
Eichenbaum, Howard
Venue
Neuron
Publisher
Elsevier BV
Published
2011-08
Volume
71
Issue
4
Pages
737-749
ISSN
0896-6273 (ISSN-L)
OpenAlex
W2011074553
Cited by
1,193
References
79
Citations by year
2026: 67 · 2025: 100 · 2024: 98 · 2023: 77 · 2022: 92 · 2021: 84 · 2020: 88 · 2019: 103 · 2018: 79 · 2017: 92 · 2016: 59 · 2015: 68 · 2014: 76 · 2013: 64 · 2012: 39
FWCI
29.57
Type
journal article
Language
en
Open access
Locations
  • Neuron (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
Funders
National Institute of Mental Health (MH-71702, MH095297, R01MH095297, P50MH071702)
Topics
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Memory Processes and Influences
  • Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
Keywords
hippocampus, time cells, sequence memory, place cells, temporal memory, neuronal ensembles, memory disambiguation
MeSH terms
Action Potentials, Animals, Behavior, Animal, Hippocampus, Humans, Male, Memory, Neurons, Odorants, Time Factors, Rats, Long-Evans, Rats

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