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Activity-dependent ectopic action potentials in regular-spiking neurons of the neocortex
INTRODUCTION: Action potentials usually travel orthodromically along a neuron’s axon, from the axon initial segment (AIS) toward the presynaptic terminals. Under some circumstances action potentials also travel in the opposite direction, antidromically, after being initiated at a distal location. Gi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10685889/ https://www.ncbi.nlm.nih.gov/pubmed/38034593 http://dx.doi.org/10.3389/fncel.2023.1267687 |
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author | Zhang, Yizhen Z. Sapantzi, Stella Lin, Alice Doelfel, Savannah R. Connors, Barry W. Theyel, Brian B. |
author_facet | Zhang, Yizhen Z. Sapantzi, Stella Lin, Alice Doelfel, Savannah R. Connors, Barry W. Theyel, Brian B. |
author_sort | Zhang, Yizhen Z. |
collection | PubMed |
description | INTRODUCTION: Action potentials usually travel orthodromically along a neuron’s axon, from the axon initial segment (AIS) toward the presynaptic terminals. Under some circumstances action potentials also travel in the opposite direction, antidromically, after being initiated at a distal location. Given their initiation at an atypical site, we refer to these events as “ectopic action potentials.” Ectopic action potentials (EAPs) were initially observed in pathological conditions including seizures and nerve injury. Several studies have described regular-spiking (RS) pyramidal neurons firing EAPs in seizure models. Under nonpathological conditions, EAPs were reported in a few populations of neurons, and our group has found that EAPs can be induced in a large proportion of parvalbumin-expressing interneurons in the neocortex. Nevertheless, to our knowledge there have been no prior reports of ectopic firing in the largest population of neurons in the neocortex, pyramidal neurons, under nonpathological conditions. METHODS: We performed in vitro recordings utilizing the whole-cell patch clamp technique. To elicit EAPs, we triggered orthodromic action potentialswith either long, progressively increasing current steps, or with trains of brief pulses at 30, 60, or 100 Hz delivered in 3 different ways, varying in stimulus and resting period duration. RESULTS: We found that a large proportion (72.7%) of neocortical RS cells from mice can fire EAPs after a specific stimulus in vitro, and that most RS cells (56.1%) are capable of firing EAPs across a broad range of stimulus conditions. Of the 37 RS neurons in which we were able to elicit EAPs, it took an average of 863.8 orthodromic action potentials delivered over the course of an average of ~81.4 s before the first EAP was seen. We observed that some cells responded to specific stimulus frequencies while less selective, suggesting frequency tuning in a subset of the cells. DISCUSSION: Our findings suggest that pyramidal cells can integrate information over long time-scales before briefly entering a mode of self-generated firing that originates in distal axons. The surprising ubiquity of EAP generation in RS cells raises interesting questions about the potential roles of ectopic spiking in information processing, cortical oscillations, and seizure susceptibility. |
format | Online Article Text |
id | pubmed-10685889 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-106858892023-11-30 Activity-dependent ectopic action potentials in regular-spiking neurons of the neocortex Zhang, Yizhen Z. Sapantzi, Stella Lin, Alice Doelfel, Savannah R. Connors, Barry W. Theyel, Brian B. Front Cell Neurosci Cellular Neuroscience INTRODUCTION: Action potentials usually travel orthodromically along a neuron’s axon, from the axon initial segment (AIS) toward the presynaptic terminals. Under some circumstances action potentials also travel in the opposite direction, antidromically, after being initiated at a distal location. Given their initiation at an atypical site, we refer to these events as “ectopic action potentials.” Ectopic action potentials (EAPs) were initially observed in pathological conditions including seizures and nerve injury. Several studies have described regular-spiking (RS) pyramidal neurons firing EAPs in seizure models. Under nonpathological conditions, EAPs were reported in a few populations of neurons, and our group has found that EAPs can be induced in a large proportion of parvalbumin-expressing interneurons in the neocortex. Nevertheless, to our knowledge there have been no prior reports of ectopic firing in the largest population of neurons in the neocortex, pyramidal neurons, under nonpathological conditions. METHODS: We performed in vitro recordings utilizing the whole-cell patch clamp technique. To elicit EAPs, we triggered orthodromic action potentialswith either long, progressively increasing current steps, or with trains of brief pulses at 30, 60, or 100 Hz delivered in 3 different ways, varying in stimulus and resting period duration. RESULTS: We found that a large proportion (72.7%) of neocortical RS cells from mice can fire EAPs after a specific stimulus in vitro, and that most RS cells (56.1%) are capable of firing EAPs across a broad range of stimulus conditions. Of the 37 RS neurons in which we were able to elicit EAPs, it took an average of 863.8 orthodromic action potentials delivered over the course of an average of ~81.4 s before the first EAP was seen. We observed that some cells responded to specific stimulus frequencies while less selective, suggesting frequency tuning in a subset of the cells. DISCUSSION: Our findings suggest that pyramidal cells can integrate information over long time-scales before briefly entering a mode of self-generated firing that originates in distal axons. The surprising ubiquity of EAP generation in RS cells raises interesting questions about the potential roles of ectopic spiking in information processing, cortical oscillations, and seizure susceptibility. Frontiers Media S.A. 2023-11-09 /pmc/articles/PMC10685889/ /pubmed/38034593 http://dx.doi.org/10.3389/fncel.2023.1267687 Text en Copyright © 2023 Zhang, Sapantzi, Lin, Doelfel, Connors and Theyel. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cellular Neuroscience Zhang, Yizhen Z. Sapantzi, Stella Lin, Alice Doelfel, Savannah R. Connors, Barry W. Theyel, Brian B. Activity-dependent ectopic action potentials in regular-spiking neurons of the neocortex |
title | Activity-dependent ectopic action potentials in regular-spiking neurons of the neocortex |
title_full | Activity-dependent ectopic action potentials in regular-spiking neurons of the neocortex |
title_fullStr | Activity-dependent ectopic action potentials in regular-spiking neurons of the neocortex |
title_full_unstemmed | Activity-dependent ectopic action potentials in regular-spiking neurons of the neocortex |
title_short | Activity-dependent ectopic action potentials in regular-spiking neurons of the neocortex |
title_sort | activity-dependent ectopic action potentials in regular-spiking neurons of the neocortex |
topic | Cellular Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10685889/ https://www.ncbi.nlm.nih.gov/pubmed/38034593 http://dx.doi.org/10.3389/fncel.2023.1267687 |
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