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High-throughput screening for agonists of ROS production in live human vascular endothelial cells

Reactive oxygen species (ROS) are important physiological molecules, and identifying agonists for ROS production can yield useful tools for future research. Here we present an optimized protocol for high-throughput screening for agonists that induce ROS production. We describe the use of a fluoresce...

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Detalles Bibliográficos
Autores principales: Sasahara, Tomoya, Hoshi, Minako
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8715207/
https://www.ncbi.nlm.nih.gov/pubmed/35005635
http://dx.doi.org/10.1016/j.xpro.2021.101053
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author Sasahara, Tomoya
Hoshi, Minako
author_facet Sasahara, Tomoya
Hoshi, Minako
author_sort Sasahara, Tomoya
collection PubMed
description Reactive oxygen species (ROS) are important physiological molecules, and identifying agonists for ROS production can yield useful tools for future research. Here we present an optimized protocol for high-throughput screening for agonists that induce ROS production. We describe the use of a fluorescent probe in human vascular endothelial cells, which can establish whether ROS production occurs in mitochondria or in the plasma membrane of live cells. For complete details on the use and execution of this profile, please refer to Sasahara et al. (2021).
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spelling pubmed-87152072022-01-06 High-throughput screening for agonists of ROS production in live human vascular endothelial cells Sasahara, Tomoya Hoshi, Minako STAR Protoc Protocol Reactive oxygen species (ROS) are important physiological molecules, and identifying agonists for ROS production can yield useful tools for future research. Here we present an optimized protocol for high-throughput screening for agonists that induce ROS production. We describe the use of a fluorescent probe in human vascular endothelial cells, which can establish whether ROS production occurs in mitochondria or in the plasma membrane of live cells. For complete details on the use and execution of this profile, please refer to Sasahara et al. (2021). Elsevier 2021-12-21 /pmc/articles/PMC8715207/ /pubmed/35005635 http://dx.doi.org/10.1016/j.xpro.2021.101053 Text en © 2021 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Protocol
Sasahara, Tomoya
Hoshi, Minako
High-throughput screening for agonists of ROS production in live human vascular endothelial cells
title High-throughput screening for agonists of ROS production in live human vascular endothelial cells
title_full High-throughput screening for agonists of ROS production in live human vascular endothelial cells
title_fullStr High-throughput screening for agonists of ROS production in live human vascular endothelial cells
title_full_unstemmed High-throughput screening for agonists of ROS production in live human vascular endothelial cells
title_short High-throughput screening for agonists of ROS production in live human vascular endothelial cells
title_sort high-throughput screening for agonists of ros production in live human vascular endothelial cells
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8715207/
https://www.ncbi.nlm.nih.gov/pubmed/35005635
http://dx.doi.org/10.1016/j.xpro.2021.101053
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