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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...

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Detalles Bibliográficos
Autores principales: Peña-Ramos, Omar, Zhou, Zheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
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)
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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
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