Skip to content
DraconiticResearch
Search Sources API
201,818 studies31 sourcesUpdated 10 min ago
PreprintCC BYbioRxiv

Cellular Determinants of CA1 Pyramidal Cell Recruitment during Sharp-Wave Ripples

  1. 1Brain Research Institute, University of Zurich, Zurich, Switzerland

Abstract

Hippocampal ripples, accompanied by highly synchronous neuronal firing, are critical for immediate offline memory consolidation, learning, and planning. However, the cellular mechanisms that determine which individual neurons are recruited to participate in action potential (AP) firing during ripples remain unclear. We investigated the membrane potential (Vm) dynamics of CA1 pyramidal cells during ripples using whole-cell recordings in awake, head-fixed mice. We found that ripple participation was strongly associated with concurrent membrane-potential depolarization on an event-to-event basis, whereas between-cell differences in overall participation propensity were jointly explained by ripple-associated depolarization and intrinsic excitability. Applying this framework across CA1 cell populations revealed that differences in recruitment between superficial and deep pyramidal cells were primarily driven by ripple-associated depolarization, counteracted by excitability. Differences between place and non-place cells were similarly driven by ripple-associated depolarization, though this effect acted in the same direction as excitability. Finally, we identified the post-ripple LFP rebound as a prominent marker of ripple diversity linked to post-ripple membrane-potential hyperpolarization at the single-neuron level. Together, these findings provide a mechanistic understanding of how CA1 pyramidal cells are selectively recruited during hippocampal ripples.

Related

  1. Bi-layered living cellular constructs promote recruitment and activation of an M2 macrophage phenotype
    Justin T. Avery, Steven M. Zabroski, Hattie E. Hensley +3
    Frontiers in immunologyPeer-reviewedCC BYFull textImmunologyEurope PMCCrossref
  2. Strategy-Dependent Recruitment of Distributed Cortical Circuits during Spatial Navigation
    Daniel A. Surinach, Mathew L. Rynes, Kapil Saxena +4
    The Journal of NeurosciencePeer-reviewedPublisher termsFull text8 citedNeurosciencePMCOpenAlex
  3. Liver-resident cellular determinants of oncolytic virotherapy in hepatocellular carcinoma: viral susceptibility and spatial immune remodeling.
    Ding Hu, Qiong Wang
    Frontiers in cell and developmental biologyPeer-reviewedCC BYFull textGenetics & genomicsEurope PMC
  4. Tissue-Resident and Effector-Memory Lymphocyte Recruitment to the Ocular Mucosa Requires CCL28/CCR10 Signaling During Recurrent HSV-1 Infection
    S. Karan, S. Prakash, M. Chhaya +2
    bioRxivPreprintCC BY-NC-NDFull textImmunologybioRxiv
  5. Awake sharp-wave ripples coincide with rhythmic cortical synchronization
    T. H. Lim, X. Zhang
    bioRxivPreprintCC BYFull textNeurosciencebioRxiv
BibTeX
@misc{angerbauer2026cellular,
  title = {{Cellular Determinants of CA1 Pyramidal Cell Recruitment during Sharp-Wave Ripples}},
  author = {R. Angerbauer and T. H. Lim and P. Jonas and F. Helmchen and X. Zhang},
  howpublished = {bioRxiv},
  year = {2026},
  month = sep,
  doi = {10.64898/2026.09.28.755157},
  url = {https://www.biorxiv.org/content/10.64898/2026.09.28.755157v1},
  note = {CC BY},
}
RIS
TY  - UNPB
TI  - Cellular Determinants of CA1 Pyramidal Cell Recruitment during Sharp-Wave Ripples
AU  - R. Angerbauer
AU  - T. H. Lim
AU  - P. Jonas
AU  - F. Helmchen
AU  - X. Zhang
PY  - 2026
DA  - 2026/09/28
PB  - bioRxiv
DO  - 10.64898/2026.09.28.755157
UR  - https://www.biorxiv.org/content/10.64898/2026.09.28.755157v1
AB  - Hippocampal ripples, accompanied by highly synchronous neuronal firing, are critical for immediate offline memory consolidation, learning, and planning. However, the cellular mechanisms that determine which individual neurons are recruited to participate in action potential (AP) firing during ripples remain unclear. We investigated the membrane potential (Vm) dynamics of CA1 pyramidal cells during ripples using whole-cell recordings in awake, head-fixed mice. We found that ripple participation was strongly associated with concurrent membrane-potential depolarization on an event-to-event basis, whereas between-cell differences in overall participation propensity were jointly explained by ripple-associated depolarization and intrinsic excitability. Applying this framework across CA1 cell populations revealed that differences in recruitment between superficial and deep pyramidal cells were primarily driven by ripple-associated depolarization, counteracted by excitability. Differences between place and non-place cells were similarly driven by ripple-associated depolarization, though this effect acted in the same direction as excitability. Finally, we identified the post-ripple LFP rebound as a prominent marker of ripple diversity linked to post-ripple membrane-potential hyperpolarization at the single-neuron level. Together, these findings provide a mechanistic understanding of how CA1 pyramidal cells are selectively recruited during hippocampal ripples.
ER  -