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Electrical Identification and Selective Microstimulation of Neuronal Compartments Based on Features of Extracellular Action Potentials
A detailed, high-spatiotemporal-resolution characterization of neuronal responses to local electrical fields and the capability of precise extracellular microstimulation of selected neurons are pivotal for studying and manipulating neuronal activity and circuits in networks and for developing neural...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4980679/ https://www.ncbi.nlm.nih.gov/pubmed/27510732 http://dx.doi.org/10.1038/srep31332 |
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author | Radivojevic, Milos Jäckel, David Altermatt, Michael Müller, Jan Viswam, Vijay Hierlemann, Andreas Bakkum, Douglas J. |
author_facet | Radivojevic, Milos Jäckel, David Altermatt, Michael Müller, Jan Viswam, Vijay Hierlemann, Andreas Bakkum, Douglas J. |
author_sort | Radivojevic, Milos |
collection | PubMed |
description | A detailed, high-spatiotemporal-resolution characterization of neuronal responses to local electrical fields and the capability of precise extracellular microstimulation of selected neurons are pivotal for studying and manipulating neuronal activity and circuits in networks and for developing neural prosthetics. Here, we studied cultured neocortical neurons by using high-density microelectrode arrays and optical imaging, complemented by the patch-clamp technique, and with the aim to correlate morphological and electrical features of neuronal compartments with their responsiveness to extracellular stimulation. We developed strategies to electrically identify any neuron in the network, while subcellular spatial resolution recording of extracellular action potential (AP) traces enabled their assignment to the axon initial segment (AIS), axonal arbor and proximal somatodendritic compartments. Stimulation at the AIS required low voltages and provided immediate, selective and reliable neuronal activation, whereas stimulation at the soma required high voltages and produced delayed and unreliable responses. Subthreshold stimulation at the soma depolarized the somatic membrane potential without eliciting APs. |
format | Online Article Text |
id | pubmed-4980679 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49806792016-08-19 Electrical Identification and Selective Microstimulation of Neuronal Compartments Based on Features of Extracellular Action Potentials Radivojevic, Milos Jäckel, David Altermatt, Michael Müller, Jan Viswam, Vijay Hierlemann, Andreas Bakkum, Douglas J. Sci Rep Article A detailed, high-spatiotemporal-resolution characterization of neuronal responses to local electrical fields and the capability of precise extracellular microstimulation of selected neurons are pivotal for studying and manipulating neuronal activity and circuits in networks and for developing neural prosthetics. Here, we studied cultured neocortical neurons by using high-density microelectrode arrays and optical imaging, complemented by the patch-clamp technique, and with the aim to correlate morphological and electrical features of neuronal compartments with their responsiveness to extracellular stimulation. We developed strategies to electrically identify any neuron in the network, while subcellular spatial resolution recording of extracellular action potential (AP) traces enabled their assignment to the axon initial segment (AIS), axonal arbor and proximal somatodendritic compartments. Stimulation at the AIS required low voltages and provided immediate, selective and reliable neuronal activation, whereas stimulation at the soma required high voltages and produced delayed and unreliable responses. Subthreshold stimulation at the soma depolarized the somatic membrane potential without eliciting APs. Nature Publishing Group 2016-08-11 /pmc/articles/PMC4980679/ /pubmed/27510732 http://dx.doi.org/10.1038/srep31332 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Radivojevic, Milos Jäckel, David Altermatt, Michael Müller, Jan Viswam, Vijay Hierlemann, Andreas Bakkum, Douglas J. Electrical Identification and Selective Microstimulation of Neuronal Compartments Based on Features of Extracellular Action Potentials |
title | Electrical Identification and Selective Microstimulation of Neuronal Compartments Based on Features of Extracellular Action Potentials |
title_full | Electrical Identification and Selective Microstimulation of Neuronal Compartments Based on Features of Extracellular Action Potentials |
title_fullStr | Electrical Identification and Selective Microstimulation of Neuronal Compartments Based on Features of Extracellular Action Potentials |
title_full_unstemmed | Electrical Identification and Selective Microstimulation of Neuronal Compartments Based on Features of Extracellular Action Potentials |
title_short | Electrical Identification and Selective Microstimulation of Neuronal Compartments Based on Features of Extracellular Action Potentials |
title_sort | electrical identification and selective microstimulation of neuronal compartments based on features of extracellular action potentials |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4980679/ https://www.ncbi.nlm.nih.gov/pubmed/27510732 http://dx.doi.org/10.1038/srep31332 |
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