Cargando…
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...
Autores principales: | , , , , , , |
---|---|
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 |
_version_ | 1783523940601167872 |
---|---|
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. |
format | Online Article Text |
id | pubmed-7170766 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT cohnjessea longtermactivitydrivesdendriticbranchelaborationofaceleganssensoryneuron AT cebulelizabethr longtermactivitydrivesdendriticbranchelaborationofaceleganssensoryneuron AT valpergagiulio longtermactivitydrivesdendriticbranchelaborationofaceleganssensoryneuron AT broselotti longtermactivitydrivesdendriticbranchelaborationofaceleganssensoryneuron AT debonomario longtermactivitydrivesdendriticbranchelaborationofaceleganssensoryneuron AT heimanmaxwellg longtermactivitydrivesdendriticbranchelaborationofaceleganssensoryneuron AT piercejonathant longtermactivitydrivesdendriticbranchelaborationofaceleganssensoryneuron |