Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Ricci, Maria, Ragonese, Francesco, Gironi, Beatrice, Paolantoni, Marco, Morresi, Assunta, Latterini, Loredana, Fioretti, Bernard, Sassi, Paola
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
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
_version_ 1783325107468369920
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
work_keys_str_mv AT riccimaria glioblastomasinglecellmicroramananalysisunderstresstreatments
AT ragonesefrancesco glioblastomasinglecellmicroramananalysisunderstresstreatments
AT gironibeatrice glioblastomasinglecellmicroramananalysisunderstresstreatments
AT paolantonimarco glioblastomasinglecellmicroramananalysisunderstresstreatments
AT morresiassunta glioblastomasinglecellmicroramananalysisunderstresstreatments
AT latteriniloredana glioblastomasinglecellmicroramananalysisunderstresstreatments
AT fiorettibernard glioblastomasinglecellmicroramananalysisunderstresstreatments
AT sassipaola glioblastomasinglecellmicroramananalysisunderstresstreatments