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Early and late place cells during postnatal development of the hippocampus

Author

Listed:
  • Chenyue Wang

    (Southern University of Science and Technology)

  • Hongjiang Yang

    (Chinese Academy of Sciences)

  • Shijie Chen

    (Southern University of Science and Technology)

  • Cheng Wang

    (Chinese Academy of Sciences
    Chinese Academy of Sciences
    Chinese Academy of Sciences
    Chinese Academy of Sciences)

  • Xiaojing Chen

    (Southern University of Science and Technology)

Abstract

A proportion of hippocampal CA1 neurons function as place cells from the onset of navigation, which are referred to as early place cells. It is not clear whether this subset of neurons is predisposed to become place cells during early stages, or if all neurons have this potential. Here, we longitudinally imaged the activity of CA1 neurons in developing male rats during navigation with both one-photon and two-photon microscopy. Our results suggested that a largely consistent population of cells functioned as early place cells, demonstrating higher spatial coding abilities across environments and a tendency to form more synchronous cell assemblies. Early place cells were present in both deep and superficial layers of CA1. Cells in the deep layer exhibited greater synchrony than those in the superficial layer during early ages. These results support the theory that an initial cognitive map is primarily shaped by a predetermined set of hippocampal cells.

Suggested Citation

  • Chenyue Wang & Hongjiang Yang & Shijie Chen & Cheng Wang & Xiaojing Chen, 2024. "Early and late place cells during postnatal development of the hippocampus," Nature Communications, Nature, vol. 15(1), pages 1-17, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-54320-z
    DOI: 10.1038/s41467-024-54320-z
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    1. Laurenz Muessig & Fabio Ribeiro Rodrigues & Tale L. Bjerknes & Benjamin W. Towse & Caswell Barry & Neil Burgess & Edvard I. Moser & May-Britt Moser & Francesca Cacucci & Thomas J. Wills, 2024. "Environment geometry alters subiculum boundary vector cell receptive fields in adulthood and early development," Nature Communications, Nature, vol. 15(1), pages 1-17, December.
    2. Benjamin Bessières & Alessio Travaglia & Todd M. Mowery & Xinying Zhang & Cristina M. Alberini, 2020. "Early life experiences selectively mature learning and memory abilities," Nature Communications, Nature, vol. 11(1), pages 1-16, December.
    3. Usman Farooq & George Dragoi, 2024. "Experience of Euclidean geometry sculpts the development and dynamics of rodent hippocampal sequential cell assemblies," Nature Communications, Nature, vol. 15(1), pages 1-24, December.
    4. Axel Kammerer & Christian Leibold, 2014. "Hippocampal Remapping Is Constrained by Sparseness rather than Capacity," PLOS Computational Biology, Public Library of Science, vol. 10(12), pages 1-12, December.
    5. Thomas Hainmueller & Marlene Bartos, 2018. "Parallel emergence of stable and dynamic memory engrams in the hippocampus," Nature, Nature, vol. 558(7709), pages 292-296, June.
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