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In vivo imaging of a PVD neuron in Caenorhabditis elegans
The nematode Caenorhabditis elegans nociceptive PVD neurons have highly ordered dendritic branches, making this an ideal model to study the development and organization of dendrites. A ser-2-promoter-driven GFP reporter line wyIs592[ser-2prom-3p::myr-GFP] provides a comprehensive visualization of PV...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7868634/ https://www.ncbi.nlm.nih.gov/pubmed/33598656 http://dx.doi.org/10.1016/j.xpro.2021.100309 |
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author | Wang, Xinjian Li, Tingting Hu, Jiawen Feng, Zhigang Zhong, Rui Nie, Wang Yang, Xiaoyan Zou, Yan |
author_facet | Wang, Xinjian Li, Tingting Hu, Jiawen Feng, Zhigang Zhong, Rui Nie, Wang Yang, Xiaoyan Zou, Yan |
author_sort | Wang, Xinjian |
collection | PubMed |
description | The nematode Caenorhabditis elegans nociceptive PVD neurons have highly ordered dendritic branches, making this an ideal model to study the development and organization of dendrites. A ser-2-promoter-driven GFP reporter line wyIs592[ser-2prom-3p::myr-GFP] provides a comprehensive visualization of PVD anatomy. Here, we describe the detailed procedures for imaging a PVD neuron using wyIs592 at late L4 larval stage in vivo by confocal microscopy. This protocol can also be applied to imaging other cells in C. elegans. For complete details on the use and execution of this protocol, please refer to Feng et al. (2020). |
format | Online Article Text |
id | pubmed-7868634 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-78686342021-02-16 In vivo imaging of a PVD neuron in Caenorhabditis elegans Wang, Xinjian Li, Tingting Hu, Jiawen Feng, Zhigang Zhong, Rui Nie, Wang Yang, Xiaoyan Zou, Yan STAR Protoc Protocol The nematode Caenorhabditis elegans nociceptive PVD neurons have highly ordered dendritic branches, making this an ideal model to study the development and organization of dendrites. A ser-2-promoter-driven GFP reporter line wyIs592[ser-2prom-3p::myr-GFP] provides a comprehensive visualization of PVD anatomy. Here, we describe the detailed procedures for imaging a PVD neuron using wyIs592 at late L4 larval stage in vivo by confocal microscopy. This protocol can also be applied to imaging other cells in C. elegans. For complete details on the use and execution of this protocol, please refer to Feng et al. (2020). Elsevier 2021-02-04 /pmc/articles/PMC7868634/ /pubmed/33598656 http://dx.doi.org/10.1016/j.xpro.2021.100309 Text en © 2021. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Protocol Wang, Xinjian Li, Tingting Hu, Jiawen Feng, Zhigang Zhong, Rui Nie, Wang Yang, Xiaoyan Zou, Yan In vivo imaging of a PVD neuron in Caenorhabditis elegans |
title | In vivo imaging of a PVD neuron in Caenorhabditis elegans |
title_full | In vivo imaging of a PVD neuron in Caenorhabditis elegans |
title_fullStr | In vivo imaging of a PVD neuron in Caenorhabditis elegans |
title_full_unstemmed | In vivo imaging of a PVD neuron in Caenorhabditis elegans |
title_short | In vivo imaging of a PVD neuron in Caenorhabditis elegans |
title_sort | in vivo imaging of a pvd neuron in caenorhabditis elegans |
topic | Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7868634/ https://www.ncbi.nlm.nih.gov/pubmed/33598656 http://dx.doi.org/10.1016/j.xpro.2021.100309 |
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