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Surpassing light-induced cell damage in vitro with novel cell culture media
Light is extensively used to study cells in real time (live cell imaging), separate cells using fluorescence activated cell sorting (FACS) and control cellular functions with light sensitive proteins (Optogenetics). However, photo-sensitive molecules inside cells and in standard cell culture media g...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5429800/ https://www.ncbi.nlm.nih.gov/pubmed/28405003 http://dx.doi.org/10.1038/s41598-017-00829-x |
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author | Stockley, John H. Evans, Kimberley Matthey, Moritz Volbracht, Katrin Agathou, Sylvia Mukanowa, Jana Burrone, Juan Káradóttir, Ragnhildur T. |
author_facet | Stockley, John H. Evans, Kimberley Matthey, Moritz Volbracht, Katrin Agathou, Sylvia Mukanowa, Jana Burrone, Juan Káradóttir, Ragnhildur T. |
author_sort | Stockley, John H. |
collection | PubMed |
description | Light is extensively used to study cells in real time (live cell imaging), separate cells using fluorescence activated cell sorting (FACS) and control cellular functions with light sensitive proteins (Optogenetics). However, photo-sensitive molecules inside cells and in standard cell culture media generate toxic by-products that interfere with cellular functions and cell viability when exposed to light. Here we show that primary cells from the rat central nervous system respond differently to photo-toxicity, in that astrocytes and microglia undergo morphological changes, while in developing neurons and oligodendrocyte progenitor cells (OPCs) it induces cellular death. To prevent photo-toxicity and to allow for long-term photo-stimulation without causing cellular damage, we formulated new photo-inert media called MEMO and NEUMO, and an antioxidant rich and serum free supplement called SOS. These new media reduced the detrimental effects caused by light and allowed cells to endure up to twenty times more light exposure without adverse effects, thus bypassing the optical constraints previously limiting experiments. |
format | Online Article Text |
id | pubmed-5429800 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-54298002017-05-15 Surpassing light-induced cell damage in vitro with novel cell culture media Stockley, John H. Evans, Kimberley Matthey, Moritz Volbracht, Katrin Agathou, Sylvia Mukanowa, Jana Burrone, Juan Káradóttir, Ragnhildur T. Sci Rep Article Light is extensively used to study cells in real time (live cell imaging), separate cells using fluorescence activated cell sorting (FACS) and control cellular functions with light sensitive proteins (Optogenetics). However, photo-sensitive molecules inside cells and in standard cell culture media generate toxic by-products that interfere with cellular functions and cell viability when exposed to light. Here we show that primary cells from the rat central nervous system respond differently to photo-toxicity, in that astrocytes and microglia undergo morphological changes, while in developing neurons and oligodendrocyte progenitor cells (OPCs) it induces cellular death. To prevent photo-toxicity and to allow for long-term photo-stimulation without causing cellular damage, we formulated new photo-inert media called MEMO and NEUMO, and an antioxidant rich and serum free supplement called SOS. These new media reduced the detrimental effects caused by light and allowed cells to endure up to twenty times more light exposure without adverse effects, thus bypassing the optical constraints previously limiting experiments. Nature Publishing Group UK 2017-04-12 /pmc/articles/PMC5429800/ /pubmed/28405003 http://dx.doi.org/10.1038/s41598-017-00829-x Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Stockley, John H. Evans, Kimberley Matthey, Moritz Volbracht, Katrin Agathou, Sylvia Mukanowa, Jana Burrone, Juan Káradóttir, Ragnhildur T. Surpassing light-induced cell damage in vitro with novel cell culture media |
title | Surpassing light-induced cell damage in vitro with novel cell culture media |
title_full | Surpassing light-induced cell damage in vitro with novel cell culture media |
title_fullStr | Surpassing light-induced cell damage in vitro with novel cell culture media |
title_full_unstemmed | Surpassing light-induced cell damage in vitro with novel cell culture media |
title_short | Surpassing light-induced cell damage in vitro with novel cell culture media |
title_sort | surpassing light-induced cell damage in vitro with novel cell culture media |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5429800/ https://www.ncbi.nlm.nih.gov/pubmed/28405003 http://dx.doi.org/10.1038/s41598-017-00829-x |
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