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An image-guided microfluidic system for single-cell lineage tracking

Cell lineage tracking is a long-standing and unresolved problem in biology. Microfluidic technologies have the potential to address this problem, by virtue of their ability to manipulate and process single-cells in a rapid, controllable and efficient manner. Indeed, when coupled with traditional ima...

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Autores principales: Aslan Kamil, Mahmut, Fourneaux, Camille, Yilmaz, Alperen, Stavros, Stavrakis, Parmentier, Romuald, Paldi, Andras, Gonin-Giraud, Sandrine, deMello, Andrew J., Gandrillon, Olivier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10393162/
https://www.ncbi.nlm.nih.gov/pubmed/37527253
http://dx.doi.org/10.1371/journal.pone.0288655
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author Aslan Kamil, Mahmut
Fourneaux, Camille
Yilmaz, Alperen
Stavros, Stavrakis
Parmentier, Romuald
Paldi, Andras
Gonin-Giraud, Sandrine
deMello, Andrew J.
Gandrillon, Olivier
author_facet Aslan Kamil, Mahmut
Fourneaux, Camille
Yilmaz, Alperen
Stavros, Stavrakis
Parmentier, Romuald
Paldi, Andras
Gonin-Giraud, Sandrine
deMello, Andrew J.
Gandrillon, Olivier
author_sort Aslan Kamil, Mahmut
collection PubMed
description Cell lineage tracking is a long-standing and unresolved problem in biology. Microfluidic technologies have the potential to address this problem, by virtue of their ability to manipulate and process single-cells in a rapid, controllable and efficient manner. Indeed, when coupled with traditional imaging approaches, microfluidic systems allow the experimentalist to follow single-cell divisions over time. Herein, we present a valve-based microfluidic system able to probe the decision-making processes of single-cells, by tracking their lineage over multiple generations. The system operates by trapping single-cells within growth chambers, allowing the trapped cells to grow and divide, isolating sister cells after a user-defined number of divisions and finally extracting them for downstream transcriptome analysis. The platform incorporates multiple cell manipulation operations, image processing-based automation for cell loading and growth monitoring, reagent addition and device washing. To demonstrate the efficacy of the microfluidic workflow, 6C2 (chicken erythroleukemia) and T2EC (primary chicken erythrocytic progenitors) cells are tracked inside the microfluidic device over two generations, with a cell viability rate in excess of 90%. Sister cells are successfully isolated after division and extracted within a 500 nL volume, which was demonstrated to be compatible with downstream single-cell RNA sequencing analysis.
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spelling pubmed-103931622023-08-02 An image-guided microfluidic system for single-cell lineage tracking Aslan Kamil, Mahmut Fourneaux, Camille Yilmaz, Alperen Stavros, Stavrakis Parmentier, Romuald Paldi, Andras Gonin-Giraud, Sandrine deMello, Andrew J. Gandrillon, Olivier PLoS One Research Article Cell lineage tracking is a long-standing and unresolved problem in biology. Microfluidic technologies have the potential to address this problem, by virtue of their ability to manipulate and process single-cells in a rapid, controllable and efficient manner. Indeed, when coupled with traditional imaging approaches, microfluidic systems allow the experimentalist to follow single-cell divisions over time. Herein, we present a valve-based microfluidic system able to probe the decision-making processes of single-cells, by tracking their lineage over multiple generations. The system operates by trapping single-cells within growth chambers, allowing the trapped cells to grow and divide, isolating sister cells after a user-defined number of divisions and finally extracting them for downstream transcriptome analysis. The platform incorporates multiple cell manipulation operations, image processing-based automation for cell loading and growth monitoring, reagent addition and device washing. To demonstrate the efficacy of the microfluidic workflow, 6C2 (chicken erythroleukemia) and T2EC (primary chicken erythrocytic progenitors) cells are tracked inside the microfluidic device over two generations, with a cell viability rate in excess of 90%. Sister cells are successfully isolated after division and extracted within a 500 nL volume, which was demonstrated to be compatible with downstream single-cell RNA sequencing analysis. Public Library of Science 2023-08-01 /pmc/articles/PMC10393162/ /pubmed/37527253 http://dx.doi.org/10.1371/journal.pone.0288655 Text en © 2023 Aslan Kamil et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Aslan Kamil, Mahmut
Fourneaux, Camille
Yilmaz, Alperen
Stavros, Stavrakis
Parmentier, Romuald
Paldi, Andras
Gonin-Giraud, Sandrine
deMello, Andrew J.
Gandrillon, Olivier
An image-guided microfluidic system for single-cell lineage tracking
title An image-guided microfluidic system for single-cell lineage tracking
title_full An image-guided microfluidic system for single-cell lineage tracking
title_fullStr An image-guided microfluidic system for single-cell lineage tracking
title_full_unstemmed An image-guided microfluidic system for single-cell lineage tracking
title_short An image-guided microfluidic system for single-cell lineage tracking
title_sort image-guided microfluidic system for single-cell lineage tracking
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10393162/
https://www.ncbi.nlm.nih.gov/pubmed/37527253
http://dx.doi.org/10.1371/journal.pone.0288655
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