Microfluidic Lab-on-a-Chip Based on UHF-Dielectrophoresis for Stemness Phenotype Characterization and Discrimination among Glioblastoma Cells.
Elisa LambertRémi ManczakElodie BarthoutSofiane SaadaElena PorcùFrancesca MauleBarbara BessetteGiampietro ViolaLuca PersanoClaire DalmayFabrice LallouéArnaud PothierPublished in: Biosensors (2021)
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: fx01 in the low-frequency range (below 500 kHz) and fx02 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.
Keyphrases
- cancer stem cells
- high throughput
- circulating tumor cells
- single cell
- high frequency
- low cost
- transcranial magnetic stimulation
- rna seq
- end stage renal disease
- peritoneal dialysis
- induced apoptosis
- prognostic factors
- stem cells
- epithelial mesenchymal transition
- chronic kidney disease
- patient reported outcomes
- label free
- cell cycle arrest
- high resolution
- randomized controlled trial
- oxidative stress
- mass spectrometry
- endoplasmic reticulum stress
- single molecule