Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Stockley, John H., Evans, Kimberley, Matthey, Moritz, Volbracht, Katrin, Agathou, Sylvia, Mukanowa, Jana, Burrone, Juan, Káradóttir, Ragnhildur T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
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
_version_ 1783236104977121280
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
work_keys_str_mv AT stockleyjohnh surpassinglightinducedcelldamageinvitrowithnovelcellculturemedia
AT evanskimberley surpassinglightinducedcelldamageinvitrowithnovelcellculturemedia
AT mattheymoritz surpassinglightinducedcelldamageinvitrowithnovelcellculturemedia
AT volbrachtkatrin surpassinglightinducedcelldamageinvitrowithnovelcellculturemedia
AT agathousylvia surpassinglightinducedcelldamageinvitrowithnovelcellculturemedia
AT mukanowajana surpassinglightinducedcelldamageinvitrowithnovelcellculturemedia
AT burronejuan surpassinglightinducedcelldamageinvitrowithnovelcellculturemedia
AT karadottirragnhildurt surpassinglightinducedcelldamageinvitrowithnovelcellculturemedia