E-Cannula reveals anatomical diversity in sharp-wave ripples as a driver for the recruitment of distinct hippocampal assemblies
Xin LiuiD, Satoshi TeradaiD, Mehrdad RamezaniiD, Jeong‐Hoon KimiD, Yichen LuiD, Andres GrosmarkiD, Attila LosonczyiD, Duygu KuzumiD
Abstract
The hippocampus plays a critical role in spatial navigation and episodic memory. However, research on in vivo hippocampal activity dynamics has mostly relied on single modalities such as electrical recordings or optical imaging, with respectively limited spatial and temporal resolution. This technical difficulty greatly impedes multi-level investigations into network state-related changes in cellular activity. To overcome these limitations, we developed the E-Cannula integrating fully transparent graphene microelectrodes with imaging-cannula. The E-Cannula enables the simultaneous electrical recording and two-photon calcium imaging from the exact same population of neurons across an anatomically extended region of the mouse hippocampal CA1 stably across several days. These large-scale simultaneous optical and electrical recordings showed that local hippocampal sharp wave ripples (SWRs) are associated with synchronous calcium events involving large neural populations in CA1. We show that SWRs exhibit spatiotemporal wave patterns along multiple axes in 2D space with different spatial extents (local or global) and temporal propagation modes (stationary or travelling). Notably, distinct SWR wave patterns were associated with, and decoded from, the selective recruitment of orthogonal CA1 cell assemblies. These results suggest that the diversity in the anatomical progression of SWRs may serve as a mechanism for the selective activation of the unique hippocampal cell assemblies extensively implicated in the encoding of distinct memories. Through these results we demonstrate the utility of the E-Cannula as a versatile neurotechnology with the potential for future integration with other optical components such as green lenses, fibers or prisms enabling the multi-modal investigation of cross-time scale population-level neural dynamics across brain regions.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 17
- FWCI
- 1.77
- Field percentile
- top 16%
- Organism
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- On CA1 ripple oscillations: reevaluating asynchronicity evidence
Robson Scheffer Teixeira, Adriano B. L. Tort·bioRxiv·Jan 29, 2025
- Sharp wave ripple coupling in zebrafish hippocampus and basolateral amygdala
Ismary Blanco, Adam Caccavano, … Katherine E. Conant·bioRxiv·Feb 7, 2023
- Sensory cortical ensembles exhibit differential coupling to ripples in distinct hippocampal subregions
Huijeong Jeong, Vijay Mohan K Namboodiri, … Mark L. Andermann·Current BiologyPeer-reviewed·Nov 22, 2023
- Defining the synaptic mechanisms that tune CA3-CA1 reactivation during sharp-wave ripples
Paola Malerba, Matthew W. Jones, Maxim Bazhenov·bioRxiv·Aug 29, 2017
- Spatiotemporal Patterns Differentiate Hippocampal Sharp-Wave Ripples from Interictal Epileptiform Discharges in Mice and Humans
Anna Maslarova, Jiyun N. Shin, … Anli A. Liu·Nature CommunicationsPeer-reviewed·Nov 26, 2025
- Hippocampal ripple-mediated convergence of spatial codes drives the emergence of cortical contextual representations
Ayaka Bota, Yuki K. Murai, … Yasunori Hayashi·bioRxiv·Mar 29, 2021