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Simultaneous Fluorescent Recordings of Extracellular ATP and IntracellularCalcium in Mammalian Cells
Extracellular ATP is a potent signaling molecule that stimulates intracellular calcium responses through purinergic (P2) receptors in mammalian cells. While extracellular ATP and intracellular calcium can be measured separately, simultaneous monitoring can offer additional insights into P2 receptor...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bio-Protocol
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7854243/ https://www.ncbi.nlm.nih.gov/pubmed/33654769 http://dx.doi.org/10.21769/BioProtoc.3242 |
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author | Mikolajewicz, Nicholas Komarova, Svetlana V |
author_facet | Mikolajewicz, Nicholas Komarova, Svetlana V |
author_sort | Mikolajewicz, Nicholas |
collection | PubMed |
description | Extracellular ATP is a potent signaling molecule that stimulates intracellular calcium responses through purinergic (P2) receptors in mammalian cells. While extracellular ATP and intracellular calcium can be measured separately, simultaneous monitoring can offer additional insights into P2 receptor physiology. This protocol takes advantage of the overlapping fluorescence spectra between the ATP-detection substrate luciferin and calcium indicator dye Fura2. Mammalian cells are loaded with Fura2-AM and live-cell recordings are acquired in the presence of a luciferin-luciferase imaging solution. This protocol allows to study stimulus-induced ATP release and directly relate changes in extracellular ATP concentration to observed calcium responses. |
format | Online Article Text |
id | pubmed-7854243 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Bio-Protocol |
record_format | MEDLINE/PubMed |
spelling | pubmed-78542432021-03-01 Simultaneous Fluorescent Recordings of Extracellular ATP and IntracellularCalcium in Mammalian Cells Mikolajewicz, Nicholas Komarova, Svetlana V Bio Protoc Methods Article Extracellular ATP is a potent signaling molecule that stimulates intracellular calcium responses through purinergic (P2) receptors in mammalian cells. While extracellular ATP and intracellular calcium can be measured separately, simultaneous monitoring can offer additional insights into P2 receptor physiology. This protocol takes advantage of the overlapping fluorescence spectra between the ATP-detection substrate luciferin and calcium indicator dye Fura2. Mammalian cells are loaded with Fura2-AM and live-cell recordings are acquired in the presence of a luciferin-luciferase imaging solution. This protocol allows to study stimulus-induced ATP release and directly relate changes in extracellular ATP concentration to observed calcium responses. Bio-Protocol 2019-05-20 /pmc/articles/PMC7854243/ /pubmed/33654769 http://dx.doi.org/10.21769/BioProtoc.3242 Text en ©Copyright Mikolajewicz and Komarova http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (CC BY 4.0). |
spellingShingle | Methods Article Mikolajewicz, Nicholas Komarova, Svetlana V Simultaneous Fluorescent Recordings of Extracellular ATP and IntracellularCalcium in Mammalian Cells |
title | Simultaneous Fluorescent Recordings of Extracellular ATP and IntracellularCalcium in Mammalian Cells |
title_full | Simultaneous Fluorescent Recordings of Extracellular ATP and IntracellularCalcium in Mammalian Cells |
title_fullStr | Simultaneous Fluorescent Recordings of Extracellular ATP and IntracellularCalcium in Mammalian Cells |
title_full_unstemmed | Simultaneous Fluorescent Recordings of Extracellular ATP and IntracellularCalcium in Mammalian Cells |
title_short | Simultaneous Fluorescent Recordings of Extracellular ATP and IntracellularCalcium in Mammalian Cells |
title_sort | simultaneous fluorescent recordings of extracellular atp and intracellularcalcium in mammalian cells |
topic | Methods Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7854243/ https://www.ncbi.nlm.nih.gov/pubmed/33654769 http://dx.doi.org/10.21769/BioProtoc.3242 |
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