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Glioblastoma single-cell microRaman analysis under stress treatments
Glioblastoma multiforme (GBM) is the most frequent malignant brain tumor characterized by highly heterogeneous subpopulations. In order to reveal the heterogeneous cell response, single cell analysis is an essential requirement. In this study, optical microscopy and Raman microspectroscopy were used...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5964071/ https://www.ncbi.nlm.nih.gov/pubmed/29789572 http://dx.doi.org/10.1038/s41598-018-26356-x |
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author | Ricci, Maria Ragonese, Francesco Gironi, Beatrice Paolantoni, Marco Morresi, Assunta Latterini, Loredana Fioretti, Bernard Sassi, Paola |
author_facet | Ricci, Maria Ragonese, Francesco Gironi, Beatrice Paolantoni, Marco Morresi, Assunta Latterini, Loredana Fioretti, Bernard Sassi, Paola |
author_sort | Ricci, Maria |
collection | PubMed |
description | Glioblastoma multiforme (GBM) is the most frequent malignant brain tumor characterized by highly heterogeneous subpopulations. In order to reveal the heterogeneous cell response, single cell analysis is an essential requirement. In this study, optical microscopy and Raman microspectroscopy were used to follow the stress response of U251 single cells adherent on a silicon substrate. Cultured cells on silicon substrate were treated with hydrogen peroxide to promote apoptosis. Under these conditions expected changes occurred after a few hours and were revealed by the reduction of cytochrome c, lipid, nucleic acid and protein Raman signals: this ensured the possibility to analyse U251 cell line as grown on Si substrate, and to monitor the response of single cells to stress conditions. As a consequence, we used microRaman to monitor the effects induced by nutrient depletion: a fast change of Raman spectra showed two different sub-populations of sensible and resistant U251 cells. Furthermore, spectral variations after DMSO addition were associated to volume changes and confirmed by morphological analysis. Thus, our results highlight the sensitivity of Raman microspectroscopy to detect rapid variations of macromolecule concentration due to oxidative stress and/or cell volume changes at the single cell level. |
format | Online Article Text |
id | pubmed-5964071 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59640712018-05-24 Glioblastoma single-cell microRaman analysis under stress treatments Ricci, Maria Ragonese, Francesco Gironi, Beatrice Paolantoni, Marco Morresi, Assunta Latterini, Loredana Fioretti, Bernard Sassi, Paola Sci Rep Article Glioblastoma multiforme (GBM) is the most frequent malignant brain tumor characterized by highly heterogeneous subpopulations. In order to reveal the heterogeneous cell response, single cell analysis is an essential requirement. In this study, optical microscopy and Raman microspectroscopy were used to follow the stress response of U251 single cells adherent on a silicon substrate. Cultured cells on silicon substrate were treated with hydrogen peroxide to promote apoptosis. Under these conditions expected changes occurred after a few hours and were revealed by the reduction of cytochrome c, lipid, nucleic acid and protein Raman signals: this ensured the possibility to analyse U251 cell line as grown on Si substrate, and to monitor the response of single cells to stress conditions. As a consequence, we used microRaman to monitor the effects induced by nutrient depletion: a fast change of Raman spectra showed two different sub-populations of sensible and resistant U251 cells. Furthermore, spectral variations after DMSO addition were associated to volume changes and confirmed by morphological analysis. Thus, our results highlight the sensitivity of Raman microspectroscopy to detect rapid variations of macromolecule concentration due to oxidative stress and/or cell volume changes at the single cell level. Nature Publishing Group UK 2018-05-22 /pmc/articles/PMC5964071/ /pubmed/29789572 http://dx.doi.org/10.1038/s41598-018-26356-x Text en © The Author(s) 2018 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 Ricci, Maria Ragonese, Francesco Gironi, Beatrice Paolantoni, Marco Morresi, Assunta Latterini, Loredana Fioretti, Bernard Sassi, Paola Glioblastoma single-cell microRaman analysis under stress treatments |
title | Glioblastoma single-cell microRaman analysis under stress treatments |
title_full | Glioblastoma single-cell microRaman analysis under stress treatments |
title_fullStr | Glioblastoma single-cell microRaman analysis under stress treatments |
title_full_unstemmed | Glioblastoma single-cell microRaman analysis under stress treatments |
title_short | Glioblastoma single-cell microRaman analysis under stress treatments |
title_sort | glioblastoma single-cell microraman analysis under stress treatments |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5964071/ https://www.ncbi.nlm.nih.gov/pubmed/29789572 http://dx.doi.org/10.1038/s41598-018-26356-x |
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