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Tracking individual action potentials throughout mammalian axonal arbors

Axons are neuronal processes specialized for conduction of action potentials (APs). The timing and temporal precision of APs when they reach each of the synapses are fundamentally important for information processing in the brain. Due to small diameters of axons, direct recording of single AP transm...

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Autores principales: Radivojevic, Milos, Franke, Felix, Altermatt, Michael, Müller, Jan, Hierlemann, Andreas, Bakkum, Douglas J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5633342/
https://www.ncbi.nlm.nih.gov/pubmed/28990925
http://dx.doi.org/10.7554/eLife.30198
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author Radivojevic, Milos
Franke, Felix
Altermatt, Michael
Müller, Jan
Hierlemann, Andreas
Bakkum, Douglas J
author_facet Radivojevic, Milos
Franke, Felix
Altermatt, Michael
Müller, Jan
Hierlemann, Andreas
Bakkum, Douglas J
author_sort Radivojevic, Milos
collection PubMed
description Axons are neuronal processes specialized for conduction of action potentials (APs). The timing and temporal precision of APs when they reach each of the synapses are fundamentally important for information processing in the brain. Due to small diameters of axons, direct recording of single AP transmission is challenging. Consequently, most knowledge about axonal conductance derives from modeling studies or indirect measurements. We demonstrate a method to noninvasively and directly record individual APs propagating along millimeter-length axonal arbors in cortical cultures with hundreds of microelectrodes at microsecond temporal resolution. We find that cortical axons conduct single APs with high temporal precision (~100 µs arrival time jitter per mm length) and reliability: in more than 8,000,000 recorded APs, we did not observe any conduction or branch-point failures. Upon high-frequency stimulation at 100 Hz, successive became slower, and their arrival time precision decreased by 20% and 12% for the 100th AP, respectively.
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spelling pubmed-56333422017-10-11 Tracking individual action potentials throughout mammalian axonal arbors Radivojevic, Milos Franke, Felix Altermatt, Michael Müller, Jan Hierlemann, Andreas Bakkum, Douglas J eLife Neuroscience Axons are neuronal processes specialized for conduction of action potentials (APs). The timing and temporal precision of APs when they reach each of the synapses are fundamentally important for information processing in the brain. Due to small diameters of axons, direct recording of single AP transmission is challenging. Consequently, most knowledge about axonal conductance derives from modeling studies or indirect measurements. We demonstrate a method to noninvasively and directly record individual APs propagating along millimeter-length axonal arbors in cortical cultures with hundreds of microelectrodes at microsecond temporal resolution. We find that cortical axons conduct single APs with high temporal precision (~100 µs arrival time jitter per mm length) and reliability: in more than 8,000,000 recorded APs, we did not observe any conduction or branch-point failures. Upon high-frequency stimulation at 100 Hz, successive became slower, and their arrival time precision decreased by 20% and 12% for the 100th AP, respectively. eLife Sciences Publications, Ltd 2017-10-09 /pmc/articles/PMC5633342/ /pubmed/28990925 http://dx.doi.org/10.7554/eLife.30198 Text en © 2017, Radivojevic et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Radivojevic, Milos
Franke, Felix
Altermatt, Michael
Müller, Jan
Hierlemann, Andreas
Bakkum, Douglas J
Tracking individual action potentials throughout mammalian axonal arbors
title Tracking individual action potentials throughout mammalian axonal arbors
title_full Tracking individual action potentials throughout mammalian axonal arbors
title_fullStr Tracking individual action potentials throughout mammalian axonal arbors
title_full_unstemmed Tracking individual action potentials throughout mammalian axonal arbors
title_short Tracking individual action potentials throughout mammalian axonal arbors
title_sort tracking individual action potentials throughout mammalian axonal arbors
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5633342/
https://www.ncbi.nlm.nih.gov/pubmed/28990925
http://dx.doi.org/10.7554/eLife.30198
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