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Measuring the acidification of the phagosomal lumen in live C. elegans embryos
In metazoans, the acidification of the phagosomal lumen is essential for the efficient degradation of cargoes. Here, we present a protocol for measuring the rate of acidification inside phagosomal lumen containing apoptotic cells in living C. elegans embryos. We describe steps for generating a worm...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10276153/ https://www.ncbi.nlm.nih.gov/pubmed/37270784 http://dx.doi.org/10.1016/j.xpro.2023.102332 |
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author | Peña-Ramos, Omar Zhou, Zheng |
author_facet | Peña-Ramos, Omar Zhou, Zheng |
author_sort | Peña-Ramos, Omar |
collection | PubMed |
description | In metazoans, the acidification of the phagosomal lumen is essential for the efficient degradation of cargoes. Here, we present a protocol for measuring the rate of acidification inside phagosomal lumen containing apoptotic cells in living C. elegans embryos. We describe steps for generating a worm population, selecting embryos, and mounting embryos on agar pads. We then detail live imaging of embryos and data analysis. This protocol is applicable to any organism in which real-time fluorescence imaging can be performed. For complete details on the use and execution of this protocol, please refer to Pena-Ramos et al. (2022).(1) |
format | Online Article Text |
id | pubmed-10276153 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-102761532023-06-18 Measuring the acidification of the phagosomal lumen in live C. elegans embryos Peña-Ramos, Omar Zhou, Zheng STAR Protoc Protocol In metazoans, the acidification of the phagosomal lumen is essential for the efficient degradation of cargoes. Here, we present a protocol for measuring the rate of acidification inside phagosomal lumen containing apoptotic cells in living C. elegans embryos. We describe steps for generating a worm population, selecting embryos, and mounting embryos on agar pads. We then detail live imaging of embryos and data analysis. This protocol is applicable to any organism in which real-time fluorescence imaging can be performed. For complete details on the use and execution of this protocol, please refer to Pena-Ramos et al. (2022).(1) Elsevier 2023-06-03 /pmc/articles/PMC10276153/ /pubmed/37270784 http://dx.doi.org/10.1016/j.xpro.2023.102332 Text en © 2023 The Author(s) https://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 Peña-Ramos, Omar Zhou, Zheng Measuring the acidification of the phagosomal lumen in live C. elegans embryos |
title | Measuring the acidification of the phagosomal lumen in live C. elegans embryos |
title_full | Measuring the acidification of the phagosomal lumen in live C. elegans embryos |
title_fullStr | Measuring the acidification of the phagosomal lumen in live C. elegans embryos |
title_full_unstemmed | Measuring the acidification of the phagosomal lumen in live C. elegans embryos |
title_short | Measuring the acidification of the phagosomal lumen in live C. elegans embryos |
title_sort | measuring the acidification of the phagosomal lumen in live c. elegans embryos |
topic | Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10276153/ https://www.ncbi.nlm.nih.gov/pubmed/37270784 http://dx.doi.org/10.1016/j.xpro.2023.102332 |
work_keys_str_mv | AT penaramosomar measuringtheacidificationofthephagosomallumeninlivecelegansembryos AT zhouzheng measuringtheacidificationofthephagosomallumeninlivecelegansembryos |