Extracellular detection of neuronal coupling

Abstract We developed a method to non-invasively detect synaptic relationships among neurons from in vitro networks. Our method uses microelectrode arrays on which neurons are cultured and from which propagation of extracellular action potentials (eAPs) in single axons are recorded at multiple elect...

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Main Authors: Elmer Guzman, Zhuowei Cheng, Paul K. Hansma, Kenneth R. Tovar, Linda R. Petzold, Kenneth S. Kosik
Format: Article
Language:English
Published: Nature Publishing Group 2021-07-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-021-94282-6
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spelling doaj-6ac560e02a154a589e0c0676a99ca60d2021-07-25T11:27:20ZengNature Publishing GroupScientific Reports2045-23222021-07-0111111110.1038/s41598-021-94282-6Extracellular detection of neuronal couplingElmer Guzman0Zhuowei Cheng1Paul K. Hansma2Kenneth R. Tovar3Linda R. Petzold4Kenneth S. Kosik5Department of Molecular, Cellular and Developmental Biology, University of California, Santa BarbaraDepartment of Computer Science, University of California, Santa BarbaraDepartment of Physics, University of California, Santa BarbaraNeuroscience Research Institute, University of California, Santa BarbaraDepartment of Computer Science, University of California, Santa BarbaraDepartment of Molecular, Cellular and Developmental Biology, University of California, Santa BarbaraAbstract We developed a method to non-invasively detect synaptic relationships among neurons from in vitro networks. Our method uses microelectrode arrays on which neurons are cultured and from which propagation of extracellular action potentials (eAPs) in single axons are recorded at multiple electrodes. Detecting eAP propagation bypasses ambiguity introduced by spike sorting. Our methods identify short latency spiking relationships between neurons with properties expected of synaptically coupled neurons, namely they were recapitulated by direct stimulation and were sensitive to changing the number of active synaptic sites. Our methods enabled us to assemble a functional subset of neuronal connectivity in our cultures.https://doi.org/10.1038/s41598-021-94282-6
collection DOAJ
language English
format Article
sources DOAJ
author Elmer Guzman
Zhuowei Cheng
Paul K. Hansma
Kenneth R. Tovar
Linda R. Petzold
Kenneth S. Kosik
spellingShingle Elmer Guzman
Zhuowei Cheng
Paul K. Hansma
Kenneth R. Tovar
Linda R. Petzold
Kenneth S. Kosik
Extracellular detection of neuronal coupling
Scientific Reports
author_facet Elmer Guzman
Zhuowei Cheng
Paul K. Hansma
Kenneth R. Tovar
Linda R. Petzold
Kenneth S. Kosik
author_sort Elmer Guzman
title Extracellular detection of neuronal coupling
title_short Extracellular detection of neuronal coupling
title_full Extracellular detection of neuronal coupling
title_fullStr Extracellular detection of neuronal coupling
title_full_unstemmed Extracellular detection of neuronal coupling
title_sort extracellular detection of neuronal coupling
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2021-07-01
description Abstract We developed a method to non-invasively detect synaptic relationships among neurons from in vitro networks. Our method uses microelectrode arrays on which neurons are cultured and from which propagation of extracellular action potentials (eAPs) in single axons are recorded at multiple electrodes. Detecting eAP propagation bypasses ambiguity introduced by spike sorting. Our methods identify short latency spiking relationships between neurons with properties expected of synaptically coupled neurons, namely they were recapitulated by direct stimulation and were sensitive to changing the number of active synaptic sites. Our methods enabled us to assemble a functional subset of neuronal connectivity in our cultures.
url https://doi.org/10.1038/s41598-021-94282-6
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AT kennethrtovar extracellulardetectionofneuronalcoupling
AT lindarpetzold extracellulardetectionofneuronalcoupling
AT kennethskosik extracellulardetectionofneuronalcoupling
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