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Bundles of Brain Microtubules Generate Electrical Oscillations
Microtubules (MTs) are long cylindrical structures of the cytoskeleton that control cell division, intracellular transport, and the shape of cells. MTs also form bundles, which are particularly prominent in neurons, where they help define axons and dendrites. MTs are bio-electrochemical transistors...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6085364/ https://www.ncbi.nlm.nih.gov/pubmed/30093720 http://dx.doi.org/10.1038/s41598-018-30453-2 |
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author | Cantero, María del Rocío Villa Etchegoyen, Cecilia Perez, Paula L. Scarinci, Noelia Cantiello, Horacio F. |
author_facet | Cantero, María del Rocío Villa Etchegoyen, Cecilia Perez, Paula L. Scarinci, Noelia Cantiello, Horacio F. |
author_sort | Cantero, María del Rocío |
collection | PubMed |
description | Microtubules (MTs) are long cylindrical structures of the cytoskeleton that control cell division, intracellular transport, and the shape of cells. MTs also form bundles, which are particularly prominent in neurons, where they help define axons and dendrites. MTs are bio-electrochemical transistors that form nonlinear electrical transmission lines. However, the electrical properties of most MT structures remain largely unknown. Here we show that bundles of brain MTs spontaneously generate electrical oscillations and bursts of electrical activity similar to action potentials. Under intracellular-like conditions, voltage-clamped MT bundles displayed electrical oscillations with a prominent fundamental frequency at 39 Hz that progressed through various periodic regimes. The electrical oscillations represented, in average, a 258% change in the ionic conductance of the MT structures. Interestingly, voltage-clamped membrane-permeabilized neurites of cultured mouse hippocampal neurons were also capable of both, generating electrical oscillations, and conducting the electrical signals along the length of the structure. Our findings indicate that electrical oscillations are an intrinsic property of brain MT bundles, which may have important implications in the control of various neuronal functions, including the gating and regulation of cytoskeleton-regulated excitable ion channels and electrical activity that may aid and extend to higher brain functions such as memory and consciousness. |
format | Online Article Text |
id | pubmed-6085364 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-60853642018-08-16 Bundles of Brain Microtubules Generate Electrical Oscillations Cantero, María del Rocío Villa Etchegoyen, Cecilia Perez, Paula L. Scarinci, Noelia Cantiello, Horacio F. Sci Rep Article Microtubules (MTs) are long cylindrical structures of the cytoskeleton that control cell division, intracellular transport, and the shape of cells. MTs also form bundles, which are particularly prominent in neurons, where they help define axons and dendrites. MTs are bio-electrochemical transistors that form nonlinear electrical transmission lines. However, the electrical properties of most MT structures remain largely unknown. Here we show that bundles of brain MTs spontaneously generate electrical oscillations and bursts of electrical activity similar to action potentials. Under intracellular-like conditions, voltage-clamped MT bundles displayed electrical oscillations with a prominent fundamental frequency at 39 Hz that progressed through various periodic regimes. The electrical oscillations represented, in average, a 258% change in the ionic conductance of the MT structures. Interestingly, voltage-clamped membrane-permeabilized neurites of cultured mouse hippocampal neurons were also capable of both, generating electrical oscillations, and conducting the electrical signals along the length of the structure. Our findings indicate that electrical oscillations are an intrinsic property of brain MT bundles, which may have important implications in the control of various neuronal functions, including the gating and regulation of cytoskeleton-regulated excitable ion channels and electrical activity that may aid and extend to higher brain functions such as memory and consciousness. Nature Publishing Group UK 2018-08-09 /pmc/articles/PMC6085364/ /pubmed/30093720 http://dx.doi.org/10.1038/s41598-018-30453-2 Text en © The Author(s) 2018 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 Cantero, María del Rocío Villa Etchegoyen, Cecilia Perez, Paula L. Scarinci, Noelia Cantiello, Horacio F. Bundles of Brain Microtubules Generate Electrical Oscillations |
title | Bundles of Brain Microtubules Generate Electrical Oscillations |
title_full | Bundles of Brain Microtubules Generate Electrical Oscillations |
title_fullStr | Bundles of Brain Microtubules Generate Electrical Oscillations |
title_full_unstemmed | Bundles of Brain Microtubules Generate Electrical Oscillations |
title_short | Bundles of Brain Microtubules Generate Electrical Oscillations |
title_sort | bundles of brain microtubules generate electrical oscillations |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6085364/ https://www.ncbi.nlm.nih.gov/pubmed/30093720 http://dx.doi.org/10.1038/s41598-018-30453-2 |
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