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Active propagation of dendritic electrical signals in C. elegans

Active propagation of electrical signals in C. elegans neurons requires ion channels capable of regenerating membrane potentials. Here we report regenerative depolarization of a major gustatory sensory neuron, ASEL. Whole-cell patch-clamp recordings in vivo showed supralinear depolarization of ASEL...

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Autores principales: Shindou, Tomomi, Ochi-Shindou, Mayumi, Murayama, Takashi, Saita, Ei-ichiro, Momohara, Yuto, Wickens, Jeffery R., Maruyama, Ichiro N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6401061/
https://www.ncbi.nlm.nih.gov/pubmed/30837592
http://dx.doi.org/10.1038/s41598-019-40158-9
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author Shindou, Tomomi
Ochi-Shindou, Mayumi
Murayama, Takashi
Saita, Ei-ichiro
Momohara, Yuto
Wickens, Jeffery R.
Maruyama, Ichiro N.
author_facet Shindou, Tomomi
Ochi-Shindou, Mayumi
Murayama, Takashi
Saita, Ei-ichiro
Momohara, Yuto
Wickens, Jeffery R.
Maruyama, Ichiro N.
author_sort Shindou, Tomomi
collection PubMed
description Active propagation of electrical signals in C. elegans neurons requires ion channels capable of regenerating membrane potentials. Here we report regenerative depolarization of a major gustatory sensory neuron, ASEL. Whole-cell patch-clamp recordings in vivo showed supralinear depolarization of ASEL upon current injection. Furthermore, stimulation of animal’s nose with NaCl evoked all-or-none membrane depolarization in ASEL. Mutant analysis showed that EGL-19, the α1 subunit of L-type voltage-gated Ca(2+) channels, is essential for regenerative depolarization of ASEL. ASEL-specific knock-down of EGL-19 by RNAi demonstrated that EGL-19 functions in C. elegans chemotaxis along an NaCl gradient. These results demonstrate that a natural substance induces regenerative all-or-none electrical signals in dendrites, and that these signals are essential for activation of sensory neurons for chemotaxis. As in other vertebrate and invertebrate nervous systems, active information processing in dendrites occurs in C. elegans, and is necessary for adaptive behavior.
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spelling pubmed-64010612019-03-07 Active propagation of dendritic electrical signals in C. elegans Shindou, Tomomi Ochi-Shindou, Mayumi Murayama, Takashi Saita, Ei-ichiro Momohara, Yuto Wickens, Jeffery R. Maruyama, Ichiro N. Sci Rep Article Active propagation of electrical signals in C. elegans neurons requires ion channels capable of regenerating membrane potentials. Here we report regenerative depolarization of a major gustatory sensory neuron, ASEL. Whole-cell patch-clamp recordings in vivo showed supralinear depolarization of ASEL upon current injection. Furthermore, stimulation of animal’s nose with NaCl evoked all-or-none membrane depolarization in ASEL. Mutant analysis showed that EGL-19, the α1 subunit of L-type voltage-gated Ca(2+) channels, is essential for regenerative depolarization of ASEL. ASEL-specific knock-down of EGL-19 by RNAi demonstrated that EGL-19 functions in C. elegans chemotaxis along an NaCl gradient. These results demonstrate that a natural substance induces regenerative all-or-none electrical signals in dendrites, and that these signals are essential for activation of sensory neurons for chemotaxis. As in other vertebrate and invertebrate nervous systems, active information processing in dendrites occurs in C. elegans, and is necessary for adaptive behavior. Nature Publishing Group UK 2019-03-05 /pmc/articles/PMC6401061/ /pubmed/30837592 http://dx.doi.org/10.1038/s41598-019-40158-9 Text en © The Author(s) 2019 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
Shindou, Tomomi
Ochi-Shindou, Mayumi
Murayama, Takashi
Saita, Ei-ichiro
Momohara, Yuto
Wickens, Jeffery R.
Maruyama, Ichiro N.
Active propagation of dendritic electrical signals in C. elegans
title Active propagation of dendritic electrical signals in C. elegans
title_full Active propagation of dendritic electrical signals in C. elegans
title_fullStr Active propagation of dendritic electrical signals in C. elegans
title_full_unstemmed Active propagation of dendritic electrical signals in C. elegans
title_short Active propagation of dendritic electrical signals in C. elegans
title_sort active propagation of dendritic electrical signals in c. elegans
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6401061/
https://www.ncbi.nlm.nih.gov/pubmed/30837592
http://dx.doi.org/10.1038/s41598-019-40158-9
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