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Theta and gamma rhythmic coding through two spike output modes in the hippocampus during spatial navigation
Hippocampal CA1 neurons generate single spikes and stereotyped bursts of spikes. However, it is unclear how individual neurons dynamically switch between these output modes and whether these two spiking outputs relay distinct information. We performed extracellular recordings in spatially navigating...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10530698/ https://www.ncbi.nlm.nih.gov/pubmed/37540599 http://dx.doi.org/10.1016/j.celrep.2023.112906 |
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author | Lowet, Eric Sheehan, Daniel J. Chialva, Ulises Pena, Rodrigo De Oliveira Mount, Rebecca A. Xiao, Sheng Zhou, Samuel L. Tseng, Hua-an Gritton, Howard Shroff, Sanaya Kondabolu, Krishnakanth Cheung, Cyrus Wang, Yangyang Piatkevich, Kiryl D. Boyden, Edward S. Mertz, Jerome Hasselmo, Michael E. Rotstein, Horacio G. Han, Xue |
author_facet | Lowet, Eric Sheehan, Daniel J. Chialva, Ulises Pena, Rodrigo De Oliveira Mount, Rebecca A. Xiao, Sheng Zhou, Samuel L. Tseng, Hua-an Gritton, Howard Shroff, Sanaya Kondabolu, Krishnakanth Cheung, Cyrus Wang, Yangyang Piatkevich, Kiryl D. Boyden, Edward S. Mertz, Jerome Hasselmo, Michael E. Rotstein, Horacio G. Han, Xue |
author_sort | Lowet, Eric |
collection | PubMed |
description | Hippocampal CA1 neurons generate single spikes and stereotyped bursts of spikes. However, it is unclear how individual neurons dynamically switch between these output modes and whether these two spiking outputs relay distinct information. We performed extracellular recordings in spatially navigating rats and cellular voltage imaging and optogenetics in awake mice. We found that spike bursts are preferentially linked to cellular and network theta rhythms (3–12 Hz) and encode an animal’s position via theta phase precession, particularly as animals are entering a place field. In contrast, single spikes exhibit additional coupling to gamma rhythms (30–100 Hz), particularly as animals leave a place field. Biophysical modeling suggests that intracellular properties alone are sufficient to explain the observed input frequency-dependent spike coding. Thus, hippocampal neurons regulate the generation of bursts and single spikes according to frequency-specific network and intracellular dynamics, suggesting that these spiking modes perform distinct computations to support spatial behavior. |
format | Online Article Text |
id | pubmed-10530698 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
record_format | MEDLINE/PubMed |
spelling | pubmed-105306982023-09-27 Theta and gamma rhythmic coding through two spike output modes in the hippocampus during spatial navigation Lowet, Eric Sheehan, Daniel J. Chialva, Ulises Pena, Rodrigo De Oliveira Mount, Rebecca A. Xiao, Sheng Zhou, Samuel L. Tseng, Hua-an Gritton, Howard Shroff, Sanaya Kondabolu, Krishnakanth Cheung, Cyrus Wang, Yangyang Piatkevich, Kiryl D. Boyden, Edward S. Mertz, Jerome Hasselmo, Michael E. Rotstein, Horacio G. Han, Xue Cell Rep Article Hippocampal CA1 neurons generate single spikes and stereotyped bursts of spikes. However, it is unclear how individual neurons dynamically switch between these output modes and whether these two spiking outputs relay distinct information. We performed extracellular recordings in spatially navigating rats and cellular voltage imaging and optogenetics in awake mice. We found that spike bursts are preferentially linked to cellular and network theta rhythms (3–12 Hz) and encode an animal’s position via theta phase precession, particularly as animals are entering a place field. In contrast, single spikes exhibit additional coupling to gamma rhythms (30–100 Hz), particularly as animals leave a place field. Biophysical modeling suggests that intracellular properties alone are sufficient to explain the observed input frequency-dependent spike coding. Thus, hippocampal neurons regulate the generation of bursts and single spikes according to frequency-specific network and intracellular dynamics, suggesting that these spiking modes perform distinct computations to support spatial behavior. 2023-08-29 2023-08-03 /pmc/articles/PMC10530698/ /pubmed/37540599 http://dx.doi.org/10.1016/j.celrep.2023.112906 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ). |
spellingShingle | Article Lowet, Eric Sheehan, Daniel J. Chialva, Ulises Pena, Rodrigo De Oliveira Mount, Rebecca A. Xiao, Sheng Zhou, Samuel L. Tseng, Hua-an Gritton, Howard Shroff, Sanaya Kondabolu, Krishnakanth Cheung, Cyrus Wang, Yangyang Piatkevich, Kiryl D. Boyden, Edward S. Mertz, Jerome Hasselmo, Michael E. Rotstein, Horacio G. Han, Xue Theta and gamma rhythmic coding through two spike output modes in the hippocampus during spatial navigation |
title | Theta and gamma rhythmic coding through two spike output modes in the hippocampus during spatial navigation |
title_full | Theta and gamma rhythmic coding through two spike output modes in the hippocampus during spatial navigation |
title_fullStr | Theta and gamma rhythmic coding through two spike output modes in the hippocampus during spatial navigation |
title_full_unstemmed | Theta and gamma rhythmic coding through two spike output modes in the hippocampus during spatial navigation |
title_short | Theta and gamma rhythmic coding through two spike output modes in the hippocampus during spatial navigation |
title_sort | theta and gamma rhythmic coding through two spike output modes in the hippocampus during spatial navigation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10530698/ https://www.ncbi.nlm.nih.gov/pubmed/37540599 http://dx.doi.org/10.1016/j.celrep.2023.112906 |
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