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A fast and reproducible cell- and 96-well plate-based method for the evaluation of P2X7 receptor activation using YO-PRO-1 fluorescent dye

The YO-PRO-1 assay provides a quantitative estimation of P2X7 receptor activation. P2X7 receptor is associated to pathological conditions including infectious, inflammatory, neurological, musculoskeletal disorders, pain and cancer. Most primary cells and cell lines from diverse origin may be used th...

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Autores principales: Rat, Patrice, Olivier, Elodie, Tanter, Caroline, Wakx, Anaïs, Dutot, Mélody
Formato: Online Artículo Texto
Lenguaje:English
Publicado: jbm 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6708926/
https://www.ncbi.nlm.nih.gov/pubmed/31453224
http://dx.doi.org/10.14440/jbm.2017.136
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author Rat, Patrice
Olivier, Elodie
Tanter, Caroline
Wakx, Anaïs
Dutot, Mélody
author_facet Rat, Patrice
Olivier, Elodie
Tanter, Caroline
Wakx, Anaïs
Dutot, Mélody
author_sort Rat, Patrice
collection PubMed
description The YO-PRO-1 assay provides a quantitative estimation of P2X7 receptor activation. P2X7 receptor is associated to pathological conditions including infectious, inflammatory, neurological, musculoskeletal disorders, pain and cancer. Most primary cells and cell lines from diverse origin may be used thanks to the ubiquitous distribution of P2X7 receptor. To study the activation of P2X7 receptor by chemicals or biological agents, we established a microplate-based cytometry protocol to accurately and rapidly quantify the activation of P2X7 receptor that leads to the formation of large pores in cell membranes. The YO-PRO-1 assay is based on the ability of cells to incorporate and bind YO-PRO-1 dye to DNA after activation of P2X7 receptor through pore formation. Cells are seeded in 96-well plates and incubated with the compound being tested for the appropriate time. The microplate is then incubated for 10 min with YO-PRO-1 staining solution. After the 10 min staining time, fluorescence signal is read using a microplate reader in 1 min. This procedure is easier and requires less handling steps than flow cytometry. 96-well plate based YO-PRO-1 assay is a reproducible and fast method to study both P2X7 receptor activation by toxic agents at subnecrotic concentrations and P2X7 receptor inhibition by antagonists.
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spelling pubmed-67089262019-08-26 A fast and reproducible cell- and 96-well plate-based method for the evaluation of P2X7 receptor activation using YO-PRO-1 fluorescent dye Rat, Patrice Olivier, Elodie Tanter, Caroline Wakx, Anaïs Dutot, Mélody J Biol Methods Protocol The YO-PRO-1 assay provides a quantitative estimation of P2X7 receptor activation. P2X7 receptor is associated to pathological conditions including infectious, inflammatory, neurological, musculoskeletal disorders, pain and cancer. Most primary cells and cell lines from diverse origin may be used thanks to the ubiquitous distribution of P2X7 receptor. To study the activation of P2X7 receptor by chemicals or biological agents, we established a microplate-based cytometry protocol to accurately and rapidly quantify the activation of P2X7 receptor that leads to the formation of large pores in cell membranes. The YO-PRO-1 assay is based on the ability of cells to incorporate and bind YO-PRO-1 dye to DNA after activation of P2X7 receptor through pore formation. Cells are seeded in 96-well plates and incubated with the compound being tested for the appropriate time. The microplate is then incubated for 10 min with YO-PRO-1 staining solution. After the 10 min staining time, fluorescence signal is read using a microplate reader in 1 min. This procedure is easier and requires less handling steps than flow cytometry. 96-well plate based YO-PRO-1 assay is a reproducible and fast method to study both P2X7 receptor activation by toxic agents at subnecrotic concentrations and P2X7 receptor inhibition by antagonists. jbm 2017-01-20 /pmc/articles/PMC6708926/ /pubmed/31453224 http://dx.doi.org/10.14440/jbm.2017.136 Text en This work is licensed under a Creative Commons Attribution 3.0 License (http://creativecommons.org/licenses/by/3.0) .
spellingShingle Protocol
Rat, Patrice
Olivier, Elodie
Tanter, Caroline
Wakx, Anaïs
Dutot, Mélody
A fast and reproducible cell- and 96-well plate-based method for the evaluation of P2X7 receptor activation using YO-PRO-1 fluorescent dye
title A fast and reproducible cell- and 96-well plate-based method for the evaluation of P2X7 receptor activation using YO-PRO-1 fluorescent dye
title_full A fast and reproducible cell- and 96-well plate-based method for the evaluation of P2X7 receptor activation using YO-PRO-1 fluorescent dye
title_fullStr A fast and reproducible cell- and 96-well plate-based method for the evaluation of P2X7 receptor activation using YO-PRO-1 fluorescent dye
title_full_unstemmed A fast and reproducible cell- and 96-well plate-based method for the evaluation of P2X7 receptor activation using YO-PRO-1 fluorescent dye
title_short A fast and reproducible cell- and 96-well plate-based method for the evaluation of P2X7 receptor activation using YO-PRO-1 fluorescent dye
title_sort fast and reproducible cell- and 96-well plate-based method for the evaluation of p2x7 receptor activation using yo-pro-1 fluorescent dye
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6708926/
https://www.ncbi.nlm.nih.gov/pubmed/31453224
http://dx.doi.org/10.14440/jbm.2017.136
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