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Long-term activity drives dendritic branch elaboration of a C. elegans sensory neuron

Neuronal activity often leads to alterations in gene expression and cellular architecture. The nematode Caenorhabditis elegans, owing to its compact translucent nervous system, is a powerful system in which to study conserved aspects of the development and plasticity of neuronal morphology. Here we...

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Detalles Bibliográficos
Autores principales: Cohn, Jesse A., Cebul, Elizabeth R., Valperga, Giulio, Brose, Lotti, de Bono, Mario, Heiman, Maxwell G., Pierce, Jonathan T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7170766/
https://www.ncbi.nlm.nih.gov/pubmed/31945343
http://dx.doi.org/10.1016/j.ydbio.2020.01.005
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author Cohn, Jesse A.
Cebul, Elizabeth R.
Valperga, Giulio
Brose, Lotti
de Bono, Mario
Heiman, Maxwell G.
Pierce, Jonathan T.
author_facet Cohn, Jesse A.
Cebul, Elizabeth R.
Valperga, Giulio
Brose, Lotti
de Bono, Mario
Heiman, Maxwell G.
Pierce, Jonathan T.
author_sort Cohn, Jesse A.
collection PubMed
description Neuronal activity often leads to alterations in gene expression and cellular architecture. The nematode Caenorhabditis elegans, owing to its compact translucent nervous system, is a powerful system in which to study conserved aspects of the development and plasticity of neuronal morphology. Here we focus on one pair of sensory neurons, termed URX, which the worm uses to sense and avoid high levels of environmental oxygen. Previous studies have reported that the URX neuron pair has variable branched endings at its dendritic sensory tip. By controlling oxygen levels and analyzing mutants, we found that these microtubule-rich branched endings grow over time as a consequence of neuronal activity in adulthood. We also find that the growth of these branches correlates with an increase in cellular sensitivity to particular ranges of oxygen that is observable in the behavior of older worms. Given the strengths of C. elegans as a model organism, URX may serve as a potent system for uncovering genes and mechanisms involved in activity-dependent morphological changes in neurons and possible adaptive changes in the aging nervous system.
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spelling pubmed-71707662020-09-21 Long-term activity drives dendritic branch elaboration of a C. elegans sensory neuron Cohn, Jesse A. Cebul, Elizabeth R. Valperga, Giulio Brose, Lotti de Bono, Mario Heiman, Maxwell G. Pierce, Jonathan T. Dev Biol Article Neuronal activity often leads to alterations in gene expression and cellular architecture. The nematode Caenorhabditis elegans, owing to its compact translucent nervous system, is a powerful system in which to study conserved aspects of the development and plasticity of neuronal morphology. Here we focus on one pair of sensory neurons, termed URX, which the worm uses to sense and avoid high levels of environmental oxygen. Previous studies have reported that the URX neuron pair has variable branched endings at its dendritic sensory tip. By controlling oxygen levels and analyzing mutants, we found that these microtubule-rich branched endings grow over time as a consequence of neuronal activity in adulthood. We also find that the growth of these branches correlates with an increase in cellular sensitivity to particular ranges of oxygen that is observable in the behavior of older worms. Given the strengths of C. elegans as a model organism, URX may serve as a potent system for uncovering genes and mechanisms involved in activity-dependent morphological changes in neurons and possible adaptive changes in the aging nervous system. Elsevier 2020-05-01 /pmc/articles/PMC7170766/ /pubmed/31945343 http://dx.doi.org/10.1016/j.ydbio.2020.01.005 Text en © 2020 MRC Laboratory of Molecular Biology http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Cohn, Jesse A.
Cebul, Elizabeth R.
Valperga, Giulio
Brose, Lotti
de Bono, Mario
Heiman, Maxwell G.
Pierce, Jonathan T.
Long-term activity drives dendritic branch elaboration of a C. elegans sensory neuron
title Long-term activity drives dendritic branch elaboration of a C. elegans sensory neuron
title_full Long-term activity drives dendritic branch elaboration of a C. elegans sensory neuron
title_fullStr Long-term activity drives dendritic branch elaboration of a C. elegans sensory neuron
title_full_unstemmed Long-term activity drives dendritic branch elaboration of a C. elegans sensory neuron
title_short Long-term activity drives dendritic branch elaboration of a C. elegans sensory neuron
title_sort long-term activity drives dendritic branch elaboration of a c. elegans sensory neuron
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7170766/
https://www.ncbi.nlm.nih.gov/pubmed/31945343
http://dx.doi.org/10.1016/j.ydbio.2020.01.005
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