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Morphology controls how hippocampal CA1 pyramidal neuron responds to uniform electric fields: a biophysical modeling study
Responses of different neurons to electric field (EF) are highly variable, which depends on intrinsic properties of cell type. Here we use multi-compartmental biophysical models to investigate how morphologic features affect EF-induced responses in hippocampal CA1 pyramidal neurons. We find that the...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5468310/ https://www.ncbi.nlm.nih.gov/pubmed/28607422 http://dx.doi.org/10.1038/s41598-017-03547-6 |
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author | Yi, Guo-Sheng Wang, Jiang Deng, Bin Wei, Xi-Le |
author_facet | Yi, Guo-Sheng Wang, Jiang Deng, Bin Wei, Xi-Le |
author_sort | Yi, Guo-Sheng |
collection | PubMed |
description | Responses of different neurons to electric field (EF) are highly variable, which depends on intrinsic properties of cell type. Here we use multi-compartmental biophysical models to investigate how morphologic features affect EF-induced responses in hippocampal CA1 pyramidal neurons. We find that the basic morphologies of neuronal elements, including diameter, length, bend, branch, and axon terminals, are all correlated with somatic depolarization through altering the current sources or sinks created by applied field. Varying them alters the EF threshold for triggering action potentials (APs), and then determines cell sensitivity to suprathreshold field. Introducing excitatory postsynaptic potential increases cell excitability and reduces morphology-dependent EF firing threshold. It is also shown that applying identical subthreshold EF results in distinct polarizations on cell membrane with different realistic morphologies. These findings shed light on the crucial role of morphologies in determining field-induced neural response from the point of view of biophysical models. The predictions are conducive to better understanding the variability in modulatory effects of EF stimulation at the cellular level, which could also aid the interpretations of how applied fields activate central nervous system neurons and affect relevant circuits. |
format | Online Article Text |
id | pubmed-5468310 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-54683102017-06-14 Morphology controls how hippocampal CA1 pyramidal neuron responds to uniform electric fields: a biophysical modeling study Yi, Guo-Sheng Wang, Jiang Deng, Bin Wei, Xi-Le Sci Rep Article Responses of different neurons to electric field (EF) are highly variable, which depends on intrinsic properties of cell type. Here we use multi-compartmental biophysical models to investigate how morphologic features affect EF-induced responses in hippocampal CA1 pyramidal neurons. We find that the basic morphologies of neuronal elements, including diameter, length, bend, branch, and axon terminals, are all correlated with somatic depolarization through altering the current sources or sinks created by applied field. Varying them alters the EF threshold for triggering action potentials (APs), and then determines cell sensitivity to suprathreshold field. Introducing excitatory postsynaptic potential increases cell excitability and reduces morphology-dependent EF firing threshold. It is also shown that applying identical subthreshold EF results in distinct polarizations on cell membrane with different realistic morphologies. These findings shed light on the crucial role of morphologies in determining field-induced neural response from the point of view of biophysical models. The predictions are conducive to better understanding the variability in modulatory effects of EF stimulation at the cellular level, which could also aid the interpretations of how applied fields activate central nervous system neurons and affect relevant circuits. Nature Publishing Group UK 2017-06-12 /pmc/articles/PMC5468310/ /pubmed/28607422 http://dx.doi.org/10.1038/s41598-017-03547-6 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Yi, Guo-Sheng Wang, Jiang Deng, Bin Wei, Xi-Le Morphology controls how hippocampal CA1 pyramidal neuron responds to uniform electric fields: a biophysical modeling study |
title | Morphology controls how hippocampal CA1 pyramidal neuron responds to uniform electric fields: a biophysical modeling study |
title_full | Morphology controls how hippocampal CA1 pyramidal neuron responds to uniform electric fields: a biophysical modeling study |
title_fullStr | Morphology controls how hippocampal CA1 pyramidal neuron responds to uniform electric fields: a biophysical modeling study |
title_full_unstemmed | Morphology controls how hippocampal CA1 pyramidal neuron responds to uniform electric fields: a biophysical modeling study |
title_short | Morphology controls how hippocampal CA1 pyramidal neuron responds to uniform electric fields: a biophysical modeling study |
title_sort | morphology controls how hippocampal ca1 pyramidal neuron responds to uniform electric fields: a biophysical modeling study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5468310/ https://www.ncbi.nlm.nih.gov/pubmed/28607422 http://dx.doi.org/10.1038/s41598-017-03547-6 |
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