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Cell culture: complications due to mechanical release of ATP and activation of purinoceptors

There is abundant evidence that ATP (adenosine 5′-triphosphate) is released from a variety of cultured cells in response to mechanical stimulation. The release mechanism involved appears to be a combination of vesicular exocytosis and connexin and pannexin hemichannels. Purinergic receptors on cultu...

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Detalles Bibliográficos
Autores principales: Burnstock, Geoffrey, Knight, Gillian E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5610203/
https://www.ncbi.nlm.nih.gov/pubmed/28434079
http://dx.doi.org/10.1007/s00441-017-2618-8
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author Burnstock, Geoffrey
Knight, Gillian E.
author_facet Burnstock, Geoffrey
Knight, Gillian E.
author_sort Burnstock, Geoffrey
collection PubMed
description There is abundant evidence that ATP (adenosine 5′-triphosphate) is released from a variety of cultured cells in response to mechanical stimulation. The release mechanism involved appears to be a combination of vesicular exocytosis and connexin and pannexin hemichannels. Purinergic receptors on cultured cells mediate both short-term purinergic signalling of secretion and long-term (trophic) signalling such as proliferation, migration, differentiation and apoptosis. We aim in this review to bring to the attention of non-purinergic researchers using tissue culture that the release of ATP in response to mechanical stress evoked by the unavoidable movement of the cells acting on functional purinergic receptors on the culture cells is likely to complicate the interpretation of their data.
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spelling pubmed-56102032017-10-05 Cell culture: complications due to mechanical release of ATP and activation of purinoceptors Burnstock, Geoffrey Knight, Gillian E. Cell Tissue Res Review There is abundant evidence that ATP (adenosine 5′-triphosphate) is released from a variety of cultured cells in response to mechanical stimulation. The release mechanism involved appears to be a combination of vesicular exocytosis and connexin and pannexin hemichannels. Purinergic receptors on cultured cells mediate both short-term purinergic signalling of secretion and long-term (trophic) signalling such as proliferation, migration, differentiation and apoptosis. We aim in this review to bring to the attention of non-purinergic researchers using tissue culture that the release of ATP in response to mechanical stress evoked by the unavoidable movement of the cells acting on functional purinergic receptors on the culture cells is likely to complicate the interpretation of their data. Springer Berlin Heidelberg 2017-04-22 2017 /pmc/articles/PMC5610203/ /pubmed/28434079 http://dx.doi.org/10.1007/s00441-017-2618-8 Text en © The Author(s) 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium, provided 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.
spellingShingle Review
Burnstock, Geoffrey
Knight, Gillian E.
Cell culture: complications due to mechanical release of ATP and activation of purinoceptors
title Cell culture: complications due to mechanical release of ATP and activation of purinoceptors
title_full Cell culture: complications due to mechanical release of ATP and activation of purinoceptors
title_fullStr Cell culture: complications due to mechanical release of ATP and activation of purinoceptors
title_full_unstemmed Cell culture: complications due to mechanical release of ATP and activation of purinoceptors
title_short Cell culture: complications due to mechanical release of ATP and activation of purinoceptors
title_sort cell culture: complications due to mechanical release of atp and activation of purinoceptors
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5610203/
https://www.ncbi.nlm.nih.gov/pubmed/28434079
http://dx.doi.org/10.1007/s00441-017-2618-8
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