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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...

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Detalles Bibliográficos
Autores principales: Mikolajewicz, Nicholas, Komarova, Svetlana V
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bio-Protocol 2019
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.
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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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