UP-DOWN states and ripples differentially modulate membrane potential dynamics across DG, CA3, and CA1 in awake mice
Abstract
Hippocampal ripples are transient population bursts that structure cortico-hippocampal communication and play a central role in memory processing. However, the mechanisms controlling ripple initiation in behaving animals remain poorly understood. Here we combine multisite extracellular and whole-cell recordings in awake mice to contrast the brain state and ripple modulation of subthreshold dynamics across hippocampal subfields. We find that entorhinal input to the dentate gyrus (DG) exhibits UP and DOWN dynamics with ripples occurring exclusively in UP states. While elevated cortical input in UP states generates depolarization in DG and CA1, it produces persistent hyperpolarization in CA3 neurons. Furthermore, growing inhibition is evident in CA3 throughout the course of the ripple buildup, while DG and CA1 neurons exhibit depolarization transients 100 ms before and during ripples. These observations highlight the importance of CA3 inhibition for ripple generation, while pre-ripple responses indicate a long and orchestrated ripple initiation process in the awake state.
Additional Information
© 2022, Kajikawa et al. This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited. Received: April 20, 2021. Preprint posted: April 22, 2021 (view preprint). Accepted: June 2, 2022. Version of Record published: July 12, 2022 (version 1). We thank Lee-Peng Mok for help with histological processing and immunohistochemistry, Maria Papadopoulou and Stijn Cassenear for help with imaging, insightful discussions and feedback on the manuscript, and Kevin Shan for help with the data processing pipeline and insightful discussion. Confocal imaging was performed at the Caltech Biological Imaging Facility. This work was supported by a Vannevar Bush Faculty Fellowship, the Mathers Foundation, the McKnight Foundation, and NIH grant RO1MH113016. The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication. Author contributions. Koichiro Kajikawa, Brad K Hulse, Conceptualization, Data curation, Formal analysis, Investigation, Methodology, Software, Validation, Visualization, Writing – review and editing; Athanassios G Siapas, Evgueniy V Lubenov, Conceptualization, Data curation, Formal analysis, Funding acquisition, Investigation, Methodology, Project administration, Resources, Software, Supervision, Validation, Visualization, Writing – original draft, Writing – review and editing. Data availability. All data analyzed during this study are included in the manuscript and supporting files. Ethics. All procedures were approved by the Institutional Animal Care and Use Committee (IACUC) at Caltech (protocols 1465, 1771) and conformed to National Institutes of Health guidelines.Attached Files
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Additional details
- PMCID
- PMC9275824
- Eprint ID
- 115980
- Resolver ID
- CaltechAUTHORS:20220729-894444000
- Vannevar Bush Faculty Fellowship
- Mathers Foundation
- McKnight Foundation
- NIH
- RO1MH113016
- Created
-
2022-08-01Created from EPrint's datestamp field
- Updated
-
2022-08-01Created from EPrint's last_modified field
- Caltech groups
- Division of Biology and Biological Engineering (BBE)