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Monitoring and assessment of lysosomal membrane damage in cultured cells using the high-content imager

Autophagy is an intracellular self-degradation process in which part of the cytoplasm, aggregates, or damaged organelles are degraded in lysosomes. Lysophagy is a specific form of selective autophagy responsible for clearing damaged lysosomes. Here, we present a protocol for inducing lysosomal damag...

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Detalles Bibliográficos
Autores principales: Tabata, Keisuke, Saeki, Marika, Yoshimori, Tamotsu, Hamasaki, Maho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10148077/
https://www.ncbi.nlm.nih.gov/pubmed/37074905
http://dx.doi.org/10.1016/j.xpro.2023.102236
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author Tabata, Keisuke
Saeki, Marika
Yoshimori, Tamotsu
Hamasaki, Maho
author_facet Tabata, Keisuke
Saeki, Marika
Yoshimori, Tamotsu
Hamasaki, Maho
author_sort Tabata, Keisuke
collection PubMed
description Autophagy is an intracellular self-degradation process in which part of the cytoplasm, aggregates, or damaged organelles are degraded in lysosomes. Lysophagy is a specific form of selective autophagy responsible for clearing damaged lysosomes. Here, we present a protocol for inducing lysosomal damage in cultured cells and assessing lysosomal damage using a high-content imager and software program. We describe steps for induction of lysosomal damage, image acquisition with spinning disk confocal microscopy, and image analysis using Pathfinder. We then detail data analysis of the clearance of damaged lysosomes. For complete details on the use and execution of this protocol, please refer to Teranishi et al. (2022).(1)
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spelling pubmed-101480772023-04-30 Monitoring and assessment of lysosomal membrane damage in cultured cells using the high-content imager Tabata, Keisuke Saeki, Marika Yoshimori, Tamotsu Hamasaki, Maho STAR Protoc Protocol Autophagy is an intracellular self-degradation process in which part of the cytoplasm, aggregates, or damaged organelles are degraded in lysosomes. Lysophagy is a specific form of selective autophagy responsible for clearing damaged lysosomes. Here, we present a protocol for inducing lysosomal damage in cultured cells and assessing lysosomal damage using a high-content imager and software program. We describe steps for induction of lysosomal damage, image acquisition with spinning disk confocal microscopy, and image analysis using Pathfinder. We then detail data analysis of the clearance of damaged lysosomes. For complete details on the use and execution of this protocol, please refer to Teranishi et al. (2022).(1) Elsevier 2023-04-18 /pmc/articles/PMC10148077/ /pubmed/37074905 http://dx.doi.org/10.1016/j.xpro.2023.102236 Text en © 2023 The Authors 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
Tabata, Keisuke
Saeki, Marika
Yoshimori, Tamotsu
Hamasaki, Maho
Monitoring and assessment of lysosomal membrane damage in cultured cells using the high-content imager
title Monitoring and assessment of lysosomal membrane damage in cultured cells using the high-content imager
title_full Monitoring and assessment of lysosomal membrane damage in cultured cells using the high-content imager
title_fullStr Monitoring and assessment of lysosomal membrane damage in cultured cells using the high-content imager
title_full_unstemmed Monitoring and assessment of lysosomal membrane damage in cultured cells using the high-content imager
title_short Monitoring and assessment of lysosomal membrane damage in cultured cells using the high-content imager
title_sort monitoring and assessment of lysosomal membrane damage in cultured cells using the high-content imager
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10148077/
https://www.ncbi.nlm.nih.gov/pubmed/37074905
http://dx.doi.org/10.1016/j.xpro.2023.102236
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