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Framework for automated sorting of neural spikes from Neuralynx-acquired tetrode recordings in freely-moving mice

BACKGROUND: Extracellular recording represents a crucial electrophysiological technique in neuroscience for studying the activity of single neurons and neuronal populations. The electrodes capture voltage traces that, with the help of analytical tools, reveal action potentials (‘spikes’) as well as...

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Autores principales: Strohl, Joshua J., Gallagher, Joseph T., Gómez, Pedro N., Glynn, Joshua M., Huerta, Patricio T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8609830/
https://www.ncbi.nlm.nih.gov/pubmed/34809706
http://dx.doi.org/10.1186/s42234-021-00079-3
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author Strohl, Joshua J.
Gallagher, Joseph T.
Gómez, Pedro N.
Glynn, Joshua M.
Huerta, Patricio T.
author_facet Strohl, Joshua J.
Gallagher, Joseph T.
Gómez, Pedro N.
Glynn, Joshua M.
Huerta, Patricio T.
author_sort Strohl, Joshua J.
collection PubMed
description BACKGROUND: Extracellular recording represents a crucial electrophysiological technique in neuroscience for studying the activity of single neurons and neuronal populations. The electrodes capture voltage traces that, with the help of analytical tools, reveal action potentials (‘spikes’) as well as local field potentials. The process of spike sorting is used for the extraction of action potentials generated by individual neurons. Until recently, spike sorting was performed with manual techniques, which are laborious and unreliable due to inherent operator bias. As neuroscientists add multiple electrodes to their probes, the high-density devices can record hundreds to thousands of neurons simultaneously, making the manual spike sorting process increasingly difficult. The advent of automated spike sorting software has offered a compelling solution to this issue and, in this study, we present a simple-to-execute framework for running an automated spike sorter. METHODS: Tetrode recordings of freely-moving mice are obtained from the CA1 region of the hippocampus as they navigate a linear track. Tetrode recordings are also acquired from the prelimbic cortex, a region of the medial prefrontal cortex, while the mice are tested in a T maze. All animals are implanted with custom-designed, 3D-printed microdrives that carry 16 electrodes, which are bundled in a 4-tetrode geometry. RESULTS: We provide an overview of a framework for analyzing single-unit data in which we have concatenated the acquisition system (Cheetah, Neuralynx) with analytical software (MATLAB) and an automated spike sorting pipeline (MountainSort). We give precise instructions on how to implement the different steps of the framework, as well as explanations of our design logic. We validate this framework by comparing manually-sorted spikes against automatically-sorted spikes, using neural recordings of the hippocampus and prelimbic cortex in freely-moving mice. CONCLUSIONS: We have efficiently integrated the MountainSort spike sorter with Neuralynx-acquired neural recordings. Our framework is easy to implement and provides a high-throughput solution. We predict that within the broad field of bioelectronic medicine, those teams that incorporate high-density neural recording devices to their armamentarium might find our framework quite valuable as they expand their analytical footprint.
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spelling pubmed-86098302021-11-29 Framework for automated sorting of neural spikes from Neuralynx-acquired tetrode recordings in freely-moving mice Strohl, Joshua J. Gallagher, Joseph T. Gómez, Pedro N. Glynn, Joshua M. Huerta, Patricio T. Bioelectron Med Methodology BACKGROUND: Extracellular recording represents a crucial electrophysiological technique in neuroscience for studying the activity of single neurons and neuronal populations. The electrodes capture voltage traces that, with the help of analytical tools, reveal action potentials (‘spikes’) as well as local field potentials. The process of spike sorting is used for the extraction of action potentials generated by individual neurons. Until recently, spike sorting was performed with manual techniques, which are laborious and unreliable due to inherent operator bias. As neuroscientists add multiple electrodes to their probes, the high-density devices can record hundreds to thousands of neurons simultaneously, making the manual spike sorting process increasingly difficult. The advent of automated spike sorting software has offered a compelling solution to this issue and, in this study, we present a simple-to-execute framework for running an automated spike sorter. METHODS: Tetrode recordings of freely-moving mice are obtained from the CA1 region of the hippocampus as they navigate a linear track. Tetrode recordings are also acquired from the prelimbic cortex, a region of the medial prefrontal cortex, while the mice are tested in a T maze. All animals are implanted with custom-designed, 3D-printed microdrives that carry 16 electrodes, which are bundled in a 4-tetrode geometry. RESULTS: We provide an overview of a framework for analyzing single-unit data in which we have concatenated the acquisition system (Cheetah, Neuralynx) with analytical software (MATLAB) and an automated spike sorting pipeline (MountainSort). We give precise instructions on how to implement the different steps of the framework, as well as explanations of our design logic. We validate this framework by comparing manually-sorted spikes against automatically-sorted spikes, using neural recordings of the hippocampus and prelimbic cortex in freely-moving mice. CONCLUSIONS: We have efficiently integrated the MountainSort spike sorter with Neuralynx-acquired neural recordings. Our framework is easy to implement and provides a high-throughput solution. We predict that within the broad field of bioelectronic medicine, those teams that incorporate high-density neural recording devices to their armamentarium might find our framework quite valuable as they expand their analytical footprint. BioMed Central 2021-11-23 /pmc/articles/PMC8609830/ /pubmed/34809706 http://dx.doi.org/10.1186/s42234-021-00079-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Methodology
Strohl, Joshua J.
Gallagher, Joseph T.
Gómez, Pedro N.
Glynn, Joshua M.
Huerta, Patricio T.
Framework for automated sorting of neural spikes from Neuralynx-acquired tetrode recordings in freely-moving mice
title Framework for automated sorting of neural spikes from Neuralynx-acquired tetrode recordings in freely-moving mice
title_full Framework for automated sorting of neural spikes from Neuralynx-acquired tetrode recordings in freely-moving mice
title_fullStr Framework for automated sorting of neural spikes from Neuralynx-acquired tetrode recordings in freely-moving mice
title_full_unstemmed Framework for automated sorting of neural spikes from Neuralynx-acquired tetrode recordings in freely-moving mice
title_short Framework for automated sorting of neural spikes from Neuralynx-acquired tetrode recordings in freely-moving mice
title_sort framework for automated sorting of neural spikes from neuralynx-acquired tetrode recordings in freely-moving mice
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8609830/
https://www.ncbi.nlm.nih.gov/pubmed/34809706
http://dx.doi.org/10.1186/s42234-021-00079-3
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