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Time-lapse live-cell imaging of pyroptosis by confocal microscopy
Pyroptosis is a type of regulated necrosis executed by gasdermin. Osmotic cell swelling and membrane perforation are the key features of pyroptosis. This protocol presents time-lapse imaging of morphological changes during pyroptosis using a confocal microscope. We describe the step-by-step ectopic...
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/PMC10679943/ https://www.ncbi.nlm.nih.gov/pubmed/37948183 http://dx.doi.org/10.1016/j.xpro.2023.102708 |
_version_ | 1785142282518790144 |
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author | Jiang, Shuai Qin, Kunpeng Sun, Li |
author_facet | Jiang, Shuai Qin, Kunpeng Sun, Li |
author_sort | Jiang, Shuai |
collection | PubMed |
description | Pyroptosis is a type of regulated necrosis executed by gasdermin. Osmotic cell swelling and membrane perforation are the key features of pyroptosis. This protocol presents time-lapse imaging of morphological changes during pyroptosis using a confocal microscope. We describe the step-by-step ectopic expression of gasdermin, cell staining with nuclear and membrane probes, and visualization of pyroptosis by time-lapse imaging. This protocol is applicable to monitoring pyroptosis in various situations. For complete details on the use and execution of this protocol, please refer to Qin et al. (2023).(1) |
format | Online Article Text |
id | pubmed-10679943 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-106799432023-11-09 Time-lapse live-cell imaging of pyroptosis by confocal microscopy Jiang, Shuai Qin, Kunpeng Sun, Li STAR Protoc Protocol Pyroptosis is a type of regulated necrosis executed by gasdermin. Osmotic cell swelling and membrane perforation are the key features of pyroptosis. This protocol presents time-lapse imaging of morphological changes during pyroptosis using a confocal microscope. We describe the step-by-step ectopic expression of gasdermin, cell staining with nuclear and membrane probes, and visualization of pyroptosis by time-lapse imaging. This protocol is applicable to monitoring pyroptosis in various situations. For complete details on the use and execution of this protocol, please refer to Qin et al. (2023).(1) Elsevier 2023-11-09 /pmc/articles/PMC10679943/ /pubmed/37948183 http://dx.doi.org/10.1016/j.xpro.2023.102708 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 Jiang, Shuai Qin, Kunpeng Sun, Li Time-lapse live-cell imaging of pyroptosis by confocal microscopy |
title | Time-lapse live-cell imaging of pyroptosis by confocal microscopy |
title_full | Time-lapse live-cell imaging of pyroptosis by confocal microscopy |
title_fullStr | Time-lapse live-cell imaging of pyroptosis by confocal microscopy |
title_full_unstemmed | Time-lapse live-cell imaging of pyroptosis by confocal microscopy |
title_short | Time-lapse live-cell imaging of pyroptosis by confocal microscopy |
title_sort | time-lapse live-cell imaging of pyroptosis by confocal microscopy |
topic | Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10679943/ https://www.ncbi.nlm.nih.gov/pubmed/37948183 http://dx.doi.org/10.1016/j.xpro.2023.102708 |
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