Selective Retrieval of Individual Cells from Microfluidic Arrays Combining Dielectrophoretic Force and Directed Hydrodynamic Flow
Hydrodynamic-based microfluidic platforms enable single-cell arraying and analysis over time. Despite the advantages of established microfluidic systems, long-term analysis and proliferation of cells selected in such devices require off-chip recovery of cells as well as an investigation of on-chip a...
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doaj-229a83181ca34afe8625785126683a082020-11-25T02:38:13ZengMDPI AGMicromachines2072-666X2020-03-0111332210.3390/mi11030322mi11030322Selective Retrieval of Individual Cells from Microfluidic Arrays Combining Dielectrophoretic Force and Directed Hydrodynamic FlowPierre-Emmanuel Thiriet0Joern Pezoldt1Gabriele Gambardella2Kevin Keim3Bart Deplancke4Carlotta Guiducci5Laboratory of Life Sciences Electronics, École Polytechnique Fédérale de Lausanne, 1015 Lausanne, CH, SwitzerlandLaboratory of Systems Biology and Genetics, École Polytechnique Fédérale de Lausanne, 1015 Lausanne, CH, SwitzerlandLaboratory of Life Sciences Electronics, École Polytechnique Fédérale de Lausanne, 1015 Lausanne, CH, SwitzerlandLaboratory of Life Sciences Electronics, École Polytechnique Fédérale de Lausanne, 1015 Lausanne, CH, SwitzerlandLaboratory of Systems Biology and Genetics, École Polytechnique Fédérale de Lausanne, 1015 Lausanne, CH, SwitzerlandLaboratory of Life Sciences Electronics, École Polytechnique Fédérale de Lausanne, 1015 Lausanne, CH, SwitzerlandHydrodynamic-based microfluidic platforms enable single-cell arraying and analysis over time. Despite the advantages of established microfluidic systems, long-term analysis and proliferation of cells selected in such devices require off-chip recovery of cells as well as an investigation of on-chip analysis on cell phenotype, requirements still largely unmet. Here, we introduce a device for single-cell isolation, selective retrieval and off-chip recovery. To this end, singularly addressable three-dimensional electrodes are embedded within a microfluidic channel, allowing the selective release of single cells from their trapping site through application of a negative dielectrophoretic (DEP) force. Selective capture and release are carried out in standard culture medium and cells can be subsequently mitigated towards a recovery well using micro-engineered hybrid SU-8/PDMS pneumatic valves. Importantly, transcriptional analysis of recovered cells revealed only marginal alteration of their molecular profile upon DEP application, underscored by minor transcriptional changes induced upon injection into the microfluidic device. Therefore, the established microfluidic system combining targeted DEP manipulation with downstream hydrodynamic coordination of single cells provides a powerful means to handle and manipulate individual cells within one device.https://www.mdpi.com/2072-666X/11/3/322single-cell microfluidicssingle-cell recoverysingle-cell arrayhydrodynamic trappingelectrokineticstridimensional electrodesdielectrophoresis (dep)mrna sequencingdrop-seq |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Pierre-Emmanuel Thiriet Joern Pezoldt Gabriele Gambardella Kevin Keim Bart Deplancke Carlotta Guiducci |
spellingShingle |
Pierre-Emmanuel Thiriet Joern Pezoldt Gabriele Gambardella Kevin Keim Bart Deplancke Carlotta Guiducci Selective Retrieval of Individual Cells from Microfluidic Arrays Combining Dielectrophoretic Force and Directed Hydrodynamic Flow Micromachines single-cell microfluidics single-cell recovery single-cell array hydrodynamic trapping electrokinetics tridimensional electrodes dielectrophoresis (dep) mrna sequencing drop-seq |
author_facet |
Pierre-Emmanuel Thiriet Joern Pezoldt Gabriele Gambardella Kevin Keim Bart Deplancke Carlotta Guiducci |
author_sort |
Pierre-Emmanuel Thiriet |
title |
Selective Retrieval of Individual Cells from Microfluidic Arrays Combining Dielectrophoretic Force and Directed Hydrodynamic Flow |
title_short |
Selective Retrieval of Individual Cells from Microfluidic Arrays Combining Dielectrophoretic Force and Directed Hydrodynamic Flow |
title_full |
Selective Retrieval of Individual Cells from Microfluidic Arrays Combining Dielectrophoretic Force and Directed Hydrodynamic Flow |
title_fullStr |
Selective Retrieval of Individual Cells from Microfluidic Arrays Combining Dielectrophoretic Force and Directed Hydrodynamic Flow |
title_full_unstemmed |
Selective Retrieval of Individual Cells from Microfluidic Arrays Combining Dielectrophoretic Force and Directed Hydrodynamic Flow |
title_sort |
selective retrieval of individual cells from microfluidic arrays combining dielectrophoretic force and directed hydrodynamic flow |
publisher |
MDPI AG |
series |
Micromachines |
issn |
2072-666X |
publishDate |
2020-03-01 |
description |
Hydrodynamic-based microfluidic platforms enable single-cell arraying and analysis over time. Despite the advantages of established microfluidic systems, long-term analysis and proliferation of cells selected in such devices require off-chip recovery of cells as well as an investigation of on-chip analysis on cell phenotype, requirements still largely unmet. Here, we introduce a device for single-cell isolation, selective retrieval and off-chip recovery. To this end, singularly addressable three-dimensional electrodes are embedded within a microfluidic channel, allowing the selective release of single cells from their trapping site through application of a negative dielectrophoretic (DEP) force. Selective capture and release are carried out in standard culture medium and cells can be subsequently mitigated towards a recovery well using micro-engineered hybrid SU-8/PDMS pneumatic valves. Importantly, transcriptional analysis of recovered cells revealed only marginal alteration of their molecular profile upon DEP application, underscored by minor transcriptional changes induced upon injection into the microfluidic device. Therefore, the established microfluidic system combining targeted DEP manipulation with downstream hydrodynamic coordination of single cells provides a powerful means to handle and manipulate individual cells within one device. |
topic |
single-cell microfluidics single-cell recovery single-cell array hydrodynamic trapping electrokinetics tridimensional electrodes dielectrophoresis (dep) mrna sequencing drop-seq |
url |
https://www.mdpi.com/2072-666X/11/3/322 |
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