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Graded spikes differentially signal neurotransmitter input in cerebrospinal fluid contacting neurons of the mouse spinal cord
The action potential and its all-or-none nature is fundamental to neural communication. Canonically, the action potential is initiated once voltage-activated Na(+) channels are activated, and their rapid kinetics of activation and inactivation give rise to the action potential’s all-or-none nature....
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9860393/ https://www.ncbi.nlm.nih.gov/pubmed/36691620 http://dx.doi.org/10.1016/j.isci.2022.105914 |
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author | Johnson, Emily Clark, Marilyn Oncul, Merve Pantiru, Andreea MacLean, Claudia Deuchars, Jim Deuchars, Susan A. Johnston, Jamie |
author_facet | Johnson, Emily Clark, Marilyn Oncul, Merve Pantiru, Andreea MacLean, Claudia Deuchars, Jim Deuchars, Susan A. Johnston, Jamie |
author_sort | Johnson, Emily |
collection | PubMed |
description | The action potential and its all-or-none nature is fundamental to neural communication. Canonically, the action potential is initiated once voltage-activated Na(+) channels are activated, and their rapid kinetics of activation and inactivation give rise to the action potential’s all-or-none nature. Here we demonstrate that cerebrospinal fluid contacting neurons (CSFcNs) surrounding the central canal of the mouse spinal cord employ a different strategy. Rather than using voltage-activated Na(+) channels to generate binary spikes, CSFcNs use two different types of voltage-activated Ca(2+) channel, enabling spikes of different amplitude. T-type Ca(2+) channels generate small amplitude spikes, whereas larger amplitude spikes require high voltage-activated Cd(2+)-sensitive Ca(2+) channels. We demonstrate that these different amplitude spikes can signal input from different transmitter systems; purinergic inputs evoke smaller T-type dependent spikes whereas cholinergic inputs evoke larger spikes that do not rely on T-type channels. Different synaptic inputs to CSFcNs can therefore be signaled by the spike amplitude. |
format | Online Article Text |
id | pubmed-9860393 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-98603932023-01-22 Graded spikes differentially signal neurotransmitter input in cerebrospinal fluid contacting neurons of the mouse spinal cord Johnson, Emily Clark, Marilyn Oncul, Merve Pantiru, Andreea MacLean, Claudia Deuchars, Jim Deuchars, Susan A. Johnston, Jamie iScience Article The action potential and its all-or-none nature is fundamental to neural communication. Canonically, the action potential is initiated once voltage-activated Na(+) channels are activated, and their rapid kinetics of activation and inactivation give rise to the action potential’s all-or-none nature. Here we demonstrate that cerebrospinal fluid contacting neurons (CSFcNs) surrounding the central canal of the mouse spinal cord employ a different strategy. Rather than using voltage-activated Na(+) channels to generate binary spikes, CSFcNs use two different types of voltage-activated Ca(2+) channel, enabling spikes of different amplitude. T-type Ca(2+) channels generate small amplitude spikes, whereas larger amplitude spikes require high voltage-activated Cd(2+)-sensitive Ca(2+) channels. We demonstrate that these different amplitude spikes can signal input from different transmitter systems; purinergic inputs evoke smaller T-type dependent spikes whereas cholinergic inputs evoke larger spikes that do not rely on T-type channels. Different synaptic inputs to CSFcNs can therefore be signaled by the spike amplitude. Elsevier 2022-12-30 /pmc/articles/PMC9860393/ /pubmed/36691620 http://dx.doi.org/10.1016/j.isci.2022.105914 Text en © 2023 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Johnson, Emily Clark, Marilyn Oncul, Merve Pantiru, Andreea MacLean, Claudia Deuchars, Jim Deuchars, Susan A. Johnston, Jamie Graded spikes differentially signal neurotransmitter input in cerebrospinal fluid contacting neurons of the mouse spinal cord |
title | Graded spikes differentially signal neurotransmitter input in cerebrospinal fluid contacting neurons of the mouse spinal cord |
title_full | Graded spikes differentially signal neurotransmitter input in cerebrospinal fluid contacting neurons of the mouse spinal cord |
title_fullStr | Graded spikes differentially signal neurotransmitter input in cerebrospinal fluid contacting neurons of the mouse spinal cord |
title_full_unstemmed | Graded spikes differentially signal neurotransmitter input in cerebrospinal fluid contacting neurons of the mouse spinal cord |
title_short | Graded spikes differentially signal neurotransmitter input in cerebrospinal fluid contacting neurons of the mouse spinal cord |
title_sort | graded spikes differentially signal neurotransmitter input in cerebrospinal fluid contacting neurons of the mouse spinal cord |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9860393/ https://www.ncbi.nlm.nih.gov/pubmed/36691620 http://dx.doi.org/10.1016/j.isci.2022.105914 |
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