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Microfluidic Lab-on-a-Chip Based on UHF-Dielectrophoresis for Stemness Phenotype Characterization and Discrimination among Glioblastoma Cells

Glioblastoma (GBM) is one of the most aggressive solid tumors, particularly due to the presence of cancer stem cells (CSCs). Nowadays, the characterization of this cell type with an efficient, fast and low-cost method remains an issue. Hence, we have developed a microfluidic lab-on-a-chip based on d...

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Autores principales: Lambert, Elisa, Manczak, Rémi, Barthout, Elodie, Saada, Sofiane, Porcù, Elena, Maule, Francesca, Bessette, Barbara, Viola, Giampietro, Persano, Luca, Dalmay, Claire, Lalloué, Fabrice, Pothier, Arnaud
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8534203/
https://www.ncbi.nlm.nih.gov/pubmed/34677344
http://dx.doi.org/10.3390/bios11100388
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author Lambert, Elisa
Manczak, Rémi
Barthout, Elodie
Saada, Sofiane
Porcù, Elena
Maule, Francesca
Bessette, Barbara
Viola, Giampietro
Persano, Luca
Dalmay, Claire
Lalloué, Fabrice
Pothier, Arnaud
author_facet Lambert, Elisa
Manczak, Rémi
Barthout, Elodie
Saada, Sofiane
Porcù, Elena
Maule, Francesca
Bessette, Barbara
Viola, Giampietro
Persano, Luca
Dalmay, Claire
Lalloué, Fabrice
Pothier, Arnaud
author_sort Lambert, Elisa
collection PubMed
description Glioblastoma (GBM) is one of the most aggressive solid tumors, particularly due to the presence of cancer stem cells (CSCs). Nowadays, the characterization of this cell type with an efficient, fast and low-cost method remains an issue. Hence, we have developed a microfluidic lab-on-a-chip based on dielectrophoresis (DEP) single cell electro-manipulation to measure the two crossover frequencies: f(x01) in the low-frequency range (below 500 kHz) and f(x02) in the ultra-high-frequency range (UHF, above 50 MHz). First, in vitro conditions were investigated. An U87-MG cell line was cultured in different conditions in order to induce an undifferentiated phenotype. Then, ex vivo GBM cells from patients’ primary cell culture were passed through the developed microfluidic system and characterized in order to reflect clinical conditions. This article demonstrates that the usual exploitation of low-frequency range DEP does not allow the discrimination of the undifferentiated GBM cells from the differentiated one. However, the presented study highlights the use of UHF-DEP as a relevant discriminant parameter. The proposed microfluidic lab-on-a-chip is able to follow the kinetics of U87-MG phenotype transformation in a CSC enrichment medium and the cancer stem cells phenotype acquirement.
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spelling pubmed-85342032021-10-23 Microfluidic Lab-on-a-Chip Based on UHF-Dielectrophoresis for Stemness Phenotype Characterization and Discrimination among Glioblastoma Cells Lambert, Elisa Manczak, Rémi Barthout, Elodie Saada, Sofiane Porcù, Elena Maule, Francesca Bessette, Barbara Viola, Giampietro Persano, Luca Dalmay, Claire Lalloué, Fabrice Pothier, Arnaud Biosensors (Basel) Article Glioblastoma (GBM) is one of the most aggressive solid tumors, particularly due to the presence of cancer stem cells (CSCs). Nowadays, the characterization of this cell type with an efficient, fast and low-cost method remains an issue. Hence, we have developed a microfluidic lab-on-a-chip based on dielectrophoresis (DEP) single cell electro-manipulation to measure the two crossover frequencies: f(x01) in the low-frequency range (below 500 kHz) and f(x02) in the ultra-high-frequency range (UHF, above 50 MHz). First, in vitro conditions were investigated. An U87-MG cell line was cultured in different conditions in order to induce an undifferentiated phenotype. Then, ex vivo GBM cells from patients’ primary cell culture were passed through the developed microfluidic system and characterized in order to reflect clinical conditions. This article demonstrates that the usual exploitation of low-frequency range DEP does not allow the discrimination of the undifferentiated GBM cells from the differentiated one. However, the presented study highlights the use of UHF-DEP as a relevant discriminant parameter. The proposed microfluidic lab-on-a-chip is able to follow the kinetics of U87-MG phenotype transformation in a CSC enrichment medium and the cancer stem cells phenotype acquirement. MDPI 2021-10-13 /pmc/articles/PMC8534203/ /pubmed/34677344 http://dx.doi.org/10.3390/bios11100388 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Lambert, Elisa
Manczak, Rémi
Barthout, Elodie
Saada, Sofiane
Porcù, Elena
Maule, Francesca
Bessette, Barbara
Viola, Giampietro
Persano, Luca
Dalmay, Claire
Lalloué, Fabrice
Pothier, Arnaud
Microfluidic Lab-on-a-Chip Based on UHF-Dielectrophoresis for Stemness Phenotype Characterization and Discrimination among Glioblastoma Cells
title Microfluidic Lab-on-a-Chip Based on UHF-Dielectrophoresis for Stemness Phenotype Characterization and Discrimination among Glioblastoma Cells
title_full Microfluidic Lab-on-a-Chip Based on UHF-Dielectrophoresis for Stemness Phenotype Characterization and Discrimination among Glioblastoma Cells
title_fullStr Microfluidic Lab-on-a-Chip Based on UHF-Dielectrophoresis for Stemness Phenotype Characterization and Discrimination among Glioblastoma Cells
title_full_unstemmed Microfluidic Lab-on-a-Chip Based on UHF-Dielectrophoresis for Stemness Phenotype Characterization and Discrimination among Glioblastoma Cells
title_short Microfluidic Lab-on-a-Chip Based on UHF-Dielectrophoresis for Stemness Phenotype Characterization and Discrimination among Glioblastoma Cells
title_sort microfluidic lab-on-a-chip based on uhf-dielectrophoresis for stemness phenotype characterization and discrimination among glioblastoma cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8534203/
https://www.ncbi.nlm.nih.gov/pubmed/34677344
http://dx.doi.org/10.3390/bios11100388
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