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Extracellular vesicles released following heat stress induce bystander effect in unstressed populations

Cells naïve to stress can display the effects of stress, such as DNA damage and apoptosis, when they are exposed to signals from stressed cells; this phenomenon is known as the bystander effect. We previously showed that bystander effect induced by ionising radiation are mediated by extracellular ve...

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Autores principales: Bewicke-Copley, Findlay, Mulcahy, Laura Ann, Jacobs, Laura Ann, Samuel, Priya, Akbar, Naveed, Pink, Ryan Charles, Carter, David Raul Francisco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5505002/
https://www.ncbi.nlm.nih.gov/pubmed/28717426
http://dx.doi.org/10.1080/20013078.2017.1340746
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author Bewicke-Copley, Findlay
Mulcahy, Laura Ann
Jacobs, Laura Ann
Samuel, Priya
Akbar, Naveed
Pink, Ryan Charles
Carter, David Raul Francisco
author_facet Bewicke-Copley, Findlay
Mulcahy, Laura Ann
Jacobs, Laura Ann
Samuel, Priya
Akbar, Naveed
Pink, Ryan Charles
Carter, David Raul Francisco
author_sort Bewicke-Copley, Findlay
collection PubMed
description Cells naïve to stress can display the effects of stress, such as DNA damage and apoptosis, when they are exposed to signals from stressed cells; this phenomenon is known as the bystander effect. We previously showed that bystander effect induced by ionising radiation are mediated by extracellular vesicles (EVs). Bystander effect can also be induced by other types of stress, including heat shock, but it is unclear whether EVs are involved. Here we show that EVs released from heat shocked cells are also able to induce bystander damage in unstressed populations. Naïve cells treated with media conditioned by heat shocked cells showed higher levels of DNA damage and apoptosis than cells treated with media from control cells. Treating naïve cells with EVs derived from media conditioned by heat shocked cells also induced a bystander effect when compared to control, with DNA damage and apoptosis increasing whilst the level of cell viability was reduced. We demonstrate that treatment of naïve cells with heat shocked cell-derived EVs leads to greater invasiveness in a trans-well Matrigel assay. Finally, we show that naïve cells treated with EVs from heat-shocked cells are more likely to survive a subsequent heat shock, suggesting that these EVs mediate an adaptive response. We propose that EVs released following stress mediate an intercellular response that leads to apparent stress in neighbouring cells but also greater robustness in the face of a subsequent insult.
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spelling pubmed-55050022017-07-17 Extracellular vesicles released following heat stress induce bystander effect in unstressed populations Bewicke-Copley, Findlay Mulcahy, Laura Ann Jacobs, Laura Ann Samuel, Priya Akbar, Naveed Pink, Ryan Charles Carter, David Raul Francisco J Extracell Vesicles Research Article Cells naïve to stress can display the effects of stress, such as DNA damage and apoptosis, when they are exposed to signals from stressed cells; this phenomenon is known as the bystander effect. We previously showed that bystander effect induced by ionising radiation are mediated by extracellular vesicles (EVs). Bystander effect can also be induced by other types of stress, including heat shock, but it is unclear whether EVs are involved. Here we show that EVs released from heat shocked cells are also able to induce bystander damage in unstressed populations. Naïve cells treated with media conditioned by heat shocked cells showed higher levels of DNA damage and apoptosis than cells treated with media from control cells. Treating naïve cells with EVs derived from media conditioned by heat shocked cells also induced a bystander effect when compared to control, with DNA damage and apoptosis increasing whilst the level of cell viability was reduced. We demonstrate that treatment of naïve cells with heat shocked cell-derived EVs leads to greater invasiveness in a trans-well Matrigel assay. Finally, we show that naïve cells treated with EVs from heat-shocked cells are more likely to survive a subsequent heat shock, suggesting that these EVs mediate an adaptive response. We propose that EVs released following stress mediate an intercellular response that leads to apparent stress in neighbouring cells but also greater robustness in the face of a subsequent insult. Taylor & Francis 2017-07-03 /pmc/articles/PMC5505002/ /pubmed/28717426 http://dx.doi.org/10.1080/20013078.2017.1340746 Text en © 2017 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Bewicke-Copley, Findlay
Mulcahy, Laura Ann
Jacobs, Laura Ann
Samuel, Priya
Akbar, Naveed
Pink, Ryan Charles
Carter, David Raul Francisco
Extracellular vesicles released following heat stress induce bystander effect in unstressed populations
title Extracellular vesicles released following heat stress induce bystander effect in unstressed populations
title_full Extracellular vesicles released following heat stress induce bystander effect in unstressed populations
title_fullStr Extracellular vesicles released following heat stress induce bystander effect in unstressed populations
title_full_unstemmed Extracellular vesicles released following heat stress induce bystander effect in unstressed populations
title_short Extracellular vesicles released following heat stress induce bystander effect in unstressed populations
title_sort extracellular vesicles released following heat stress induce bystander effect in unstressed populations
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5505002/
https://www.ncbi.nlm.nih.gov/pubmed/28717426
http://dx.doi.org/10.1080/20013078.2017.1340746
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