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Linking hippocampal multiplexed tuning, Hebbian plasticity and navigation

Author

Listed:
  • Jason J. Moore

    (University of California at Los Angeles
    University of California at Los Angeles)

  • Jesse D. Cushman

    (University of California at Los Angeles
    University of California at Los Angeles)

  • Lavanya Acharya

    (University of California at Los Angeles
    University of California at Los Angeles)

  • Briana Popeney

    (University of California at Los Angeles
    University of California at Los Angeles)

  • Mayank R. Mehta

    (University of California at Los Angeles
    University of California at Los Angeles
    University of California at Los Angeles
    University of California at Los Angeles)

Abstract

Three major pillars of hippocampal function are spatial navigation1, Hebbian synaptic plasticity2 and spatial selectivity3. The hippocampus is also implicated in episodic memory4, but the precise link between these four functions is missing. Here we report the multiplexed selectivity of dorsal CA1 neurons while rats performed a virtual navigation task using only distal visual cues5, similar to the standard water maze test of spatial memory1. Neural responses primarily encoded path distance from the start point and the head angle of rats, with a weak allocentric spatial component similar to that in primates but substantially weaker than in rodents in the real world. Often, the same cells multiplexed and encoded path distance, angle and allocentric position in a sequence, thus encoding a journey-specific episode. The strength of neural activity and tuning strongly correlated with performance, with a temporal relationship indicating neural responses influencing behaviour and vice versa. Consistent with computational models of associative and causal Hebbian learning6,7, neural responses showed increasing clustering8 and became better predictors of behaviourally relevant variables, with the average neurometric curves exceeding and converging to psychometric curves. Thus, hippocampal neurons multiplex and exhibit highly plastic, task- and experience-dependent tuning to path-centric and allocentric variables to form episodic sequences supporting navigation.

Suggested Citation

  • Jason J. Moore & Jesse D. Cushman & Lavanya Acharya & Briana Popeney & Mayank R. Mehta, 2021. "Linking hippocampal multiplexed tuning, Hebbian plasticity and navigation," Nature, Nature, vol. 599(7885), pages 442-448, November.
  • Handle: RePEc:nat:nature:v:599:y:2021:i:7885:d:10.1038_s41586-021-03989-z
    DOI: 10.1038/s41586-021-03989-z
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    Cited by:

    1. M. Jerome Beetz & Christian Kraus & Basil el Jundi, 2023. "Neural representation of goal direction in the monarch butterfly brain," Nature Communications, Nature, vol. 14(1), pages 1-13, December.
    2. Oliver Barnstedt & Petra Mocellin & Stefan Remy, 2024. "A hippocampus-accumbens code guides goal-directed appetitive behavior," Nature Communications, Nature, vol. 15(1), pages 1-20, December.
    3. Diego B. Piza & Benjamin W. Corrigan & Roberto A. Gulli & Sonia Carmo & A. Claudio Cuello & Lyle Muller & Julio Martinez-Trujillo, 2024. "Primacy of vision shapes behavioral strategies and neural substrates of spatial navigation in marmoset hippocampus," Nature Communications, Nature, vol. 15(1), pages 1-21, December.
    4. Guillaume Etter & Suzanne Veldt & Jisoo Choi & Sylvain Williams, 2023. "Optogenetic frequency scrambling of hippocampal theta oscillations dissociates working memory retrieval from hippocampal spatiotemporal codes," Nature Communications, Nature, vol. 14(1), pages 1-18, December.
    5. Matteo Saponati & Martin Vinck, 2023. "Sequence anticipation and spike-timing-dependent plasticity emerge from a predictive learning rule," Nature Communications, Nature, vol. 14(1), pages 1-13, December.

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