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LUCS (Light-Up Cell System), a universal high throughput assay for homeostasis evaluation in live cells
Observations of fluorescent cyanine dye behavior under illumination at 500 nm lead to a novel concept in cell biology allowing the development of a new live cell assay called LUCS, for Light-Up Cell System, measuring homeostasis in live cells. Optimization of the LUCS process resulted in a standardi...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5741755/ https://www.ncbi.nlm.nih.gov/pubmed/29273711 http://dx.doi.org/10.1038/s41598-017-18211-2 |
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author | Derick, Sylvain Gironde, Camille Perio, Pierre Reybier, Karine Nepveu, Françoise Jauneau, Alain Furger, Christophe |
author_facet | Derick, Sylvain Gironde, Camille Perio, Pierre Reybier, Karine Nepveu, Françoise Jauneau, Alain Furger, Christophe |
author_sort | Derick, Sylvain |
collection | PubMed |
description | Observations of fluorescent cyanine dye behavior under illumination at 500 nm lead to a novel concept in cell biology allowing the development of a new live cell assay called LUCS, for Light-Up Cell System, measuring homeostasis in live cells. Optimization of the LUCS process resulted in a standardized, straightforward and high throughput assay with applications in toxicity assessment. The mechanisms of the LUCS process were investigated. Electron Paramagnetic Resonance experiments showed that the singlet oxygen and hydroxyl radical are involved downstream of the light effect, presumably leading to deleterious oxidative stress that massively opens access of the dye to its intracellular target. Reversible modulation of LUCS by both verapamil and proton availability indicated that plasma membrane proton/cation antiporters, possibly of the MATE drug efflux transport family, are involved. A mechanistic model is presented. Our data show that intracellular oxidation can be controlled by tuning light energy, opening applications in regulatory purposes, anti-oxidant research, chemotherapy efficacy and dynamic phototherapy strategies. |
format | Online Article Text |
id | pubmed-5741755 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57417552018-01-03 LUCS (Light-Up Cell System), a universal high throughput assay for homeostasis evaluation in live cells Derick, Sylvain Gironde, Camille Perio, Pierre Reybier, Karine Nepveu, Françoise Jauneau, Alain Furger, Christophe Sci Rep Article Observations of fluorescent cyanine dye behavior under illumination at 500 nm lead to a novel concept in cell biology allowing the development of a new live cell assay called LUCS, for Light-Up Cell System, measuring homeostasis in live cells. Optimization of the LUCS process resulted in a standardized, straightforward and high throughput assay with applications in toxicity assessment. The mechanisms of the LUCS process were investigated. Electron Paramagnetic Resonance experiments showed that the singlet oxygen and hydroxyl radical are involved downstream of the light effect, presumably leading to deleterious oxidative stress that massively opens access of the dye to its intracellular target. Reversible modulation of LUCS by both verapamil and proton availability indicated that plasma membrane proton/cation antiporters, possibly of the MATE drug efflux transport family, are involved. A mechanistic model is presented. Our data show that intracellular oxidation can be controlled by tuning light energy, opening applications in regulatory purposes, anti-oxidant research, chemotherapy efficacy and dynamic phototherapy strategies. Nature Publishing Group UK 2017-12-22 /pmc/articles/PMC5741755/ /pubmed/29273711 http://dx.doi.org/10.1038/s41598-017-18211-2 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Derick, Sylvain Gironde, Camille Perio, Pierre Reybier, Karine Nepveu, Françoise Jauneau, Alain Furger, Christophe LUCS (Light-Up Cell System), a universal high throughput assay for homeostasis evaluation in live cells |
title | LUCS (Light-Up Cell System), a universal high throughput assay for homeostasis evaluation in live cells |
title_full | LUCS (Light-Up Cell System), a universal high throughput assay for homeostasis evaluation in live cells |
title_fullStr | LUCS (Light-Up Cell System), a universal high throughput assay for homeostasis evaluation in live cells |
title_full_unstemmed | LUCS (Light-Up Cell System), a universal high throughput assay for homeostasis evaluation in live cells |
title_short | LUCS (Light-Up Cell System), a universal high throughput assay for homeostasis evaluation in live cells |
title_sort | lucs (light-up cell system), a universal high throughput assay for homeostasis evaluation in live cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5741755/ https://www.ncbi.nlm.nih.gov/pubmed/29273711 http://dx.doi.org/10.1038/s41598-017-18211-2 |
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