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Reactive oxygen species and nitric oxide signaling in bystander cells

It is now well accepted that radiation induced bystander effects can occur in cells exposed to media from irradiated cells. The aim of this study was to follow the bystander cells in real time following addition of media from irradiated cells and to determine the effect of inhibiting these signals....

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Autores principales: Jella, Kishore Kumar, Moriarty, Roisin, McClean, Brendan, Byrne, Hugh J., Lyng, Fiona M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5886541/
https://www.ncbi.nlm.nih.gov/pubmed/29621312
http://dx.doi.org/10.1371/journal.pone.0195371
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author Jella, Kishore Kumar
Moriarty, Roisin
McClean, Brendan
Byrne, Hugh J.
Lyng, Fiona M.
author_facet Jella, Kishore Kumar
Moriarty, Roisin
McClean, Brendan
Byrne, Hugh J.
Lyng, Fiona M.
author_sort Jella, Kishore Kumar
collection PubMed
description It is now well accepted that radiation induced bystander effects can occur in cells exposed to media from irradiated cells. The aim of this study was to follow the bystander cells in real time following addition of media from irradiated cells and to determine the effect of inhibiting these signals. A human keratinocyte cell line, HaCaT cells, was irradiated (0.005, 0.05 and 0.5 Gy) with γ irradiation, conditioned medium was harvested after one hour and added to recipient bystander cells. Reactive oxygen species, nitric oxide, Glutathione levels, caspase activation, cytotoxicity and cell viability was measured after the addition of irradiated cell conditioned media to bystander cells. Reactive oxygen species and nitric oxide levels in bystander cells treated with 0.5Gy ICCM were analysed in real time using time lapse fluorescence microscopy. The levels of reactive oxygen species were also measured in real time after the addition of extracellular signal-regulated kinase and c-Jun amino-terminal kinase pathway inhibitors. ROS and glutathione levels were observed to increase after the addition of irradiated cell conditioned media (0.005, 0.05 and 0.5 Gy ICCM). Caspase activation was found to increase 4 hours after irradiated cell conditioned media treatment (0.005, 0.05 and 0.5 Gy ICCM) and this increase was observed up to 8 hours and there after a reduction in caspase activation was observed. A decrease in cell viability was observed but no major change in cytotoxicity was found in HaCaT cells after treatment with irradiated cell conditioned media (0.005, 0.05 and 0.5 Gy ICCM). This study involved the identification of key signaling molecules such as reactive oxygen species, nitric oxide, glutathione and caspases generated in bystander cells. These results suggest a clear connection between reactive oxygen species and cell survival pathways with persistent production of reactive oxygen species and nitric oxide in bystander cells following exposure to irradiated cell conditioned media.
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spelling pubmed-58865412018-04-20 Reactive oxygen species and nitric oxide signaling in bystander cells Jella, Kishore Kumar Moriarty, Roisin McClean, Brendan Byrne, Hugh J. Lyng, Fiona M. PLoS One Research Article It is now well accepted that radiation induced bystander effects can occur in cells exposed to media from irradiated cells. The aim of this study was to follow the bystander cells in real time following addition of media from irradiated cells and to determine the effect of inhibiting these signals. A human keratinocyte cell line, HaCaT cells, was irradiated (0.005, 0.05 and 0.5 Gy) with γ irradiation, conditioned medium was harvested after one hour and added to recipient bystander cells. Reactive oxygen species, nitric oxide, Glutathione levels, caspase activation, cytotoxicity and cell viability was measured after the addition of irradiated cell conditioned media to bystander cells. Reactive oxygen species and nitric oxide levels in bystander cells treated with 0.5Gy ICCM were analysed in real time using time lapse fluorescence microscopy. The levels of reactive oxygen species were also measured in real time after the addition of extracellular signal-regulated kinase and c-Jun amino-terminal kinase pathway inhibitors. ROS and glutathione levels were observed to increase after the addition of irradiated cell conditioned media (0.005, 0.05 and 0.5 Gy ICCM). Caspase activation was found to increase 4 hours after irradiated cell conditioned media treatment (0.005, 0.05 and 0.5 Gy ICCM) and this increase was observed up to 8 hours and there after a reduction in caspase activation was observed. A decrease in cell viability was observed but no major change in cytotoxicity was found in HaCaT cells after treatment with irradiated cell conditioned media (0.005, 0.05 and 0.5 Gy ICCM). This study involved the identification of key signaling molecules such as reactive oxygen species, nitric oxide, glutathione and caspases generated in bystander cells. These results suggest a clear connection between reactive oxygen species and cell survival pathways with persistent production of reactive oxygen species and nitric oxide in bystander cells following exposure to irradiated cell conditioned media. Public Library of Science 2018-04-05 /pmc/articles/PMC5886541/ /pubmed/29621312 http://dx.doi.org/10.1371/journal.pone.0195371 Text en © 2018 Jella et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Jella, Kishore Kumar
Moriarty, Roisin
McClean, Brendan
Byrne, Hugh J.
Lyng, Fiona M.
Reactive oxygen species and nitric oxide signaling in bystander cells
title Reactive oxygen species and nitric oxide signaling in bystander cells
title_full Reactive oxygen species and nitric oxide signaling in bystander cells
title_fullStr Reactive oxygen species and nitric oxide signaling in bystander cells
title_full_unstemmed Reactive oxygen species and nitric oxide signaling in bystander cells
title_short Reactive oxygen species and nitric oxide signaling in bystander cells
title_sort reactive oxygen species and nitric oxide signaling in bystander cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5886541/
https://www.ncbi.nlm.nih.gov/pubmed/29621312
http://dx.doi.org/10.1371/journal.pone.0195371
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