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Electrofusion of single cells in picoliter droplets
We present a microfluidic chip that enables electrofusion of cells in microdroplets, with exchange of nuclear components. It is shown, to our knowledge for the first time, electrofusion of two HL60 cells, inside a microdroplet. This is the crucial intermediate step for controlled hybridoma formation...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5829161/ https://www.ncbi.nlm.nih.gov/pubmed/29487332 http://dx.doi.org/10.1038/s41598-018-21993-8 |
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author | Schoeman, Rogier M. van den Beld, Wesley T. E. Kemna, Evelien W. M. Wolbers, Floor Eijkel, Jan C. T. van den Berg, Albert |
author_facet | Schoeman, Rogier M. van den Beld, Wesley T. E. Kemna, Evelien W. M. Wolbers, Floor Eijkel, Jan C. T. van den Berg, Albert |
author_sort | Schoeman, Rogier M. |
collection | PubMed |
description | We present a microfluidic chip that enables electrofusion of cells in microdroplets, with exchange of nuclear components. It is shown, to our knowledge for the first time, electrofusion of two HL60 cells, inside a microdroplet. This is the crucial intermediate step for controlled hybridoma formation where a B cell is electrofused with a myeloma cell. We use a microfluidic device consisting of a microchannel structure in PDMS bonded to a glass substrate through which droplets with two differently stained HL60 cells are transported. An array of six recessed platinum electrode pairs is used for electrofusion. When applying six voltage pulses of 2–3 V, the membrane electrical field is about 1 MV/cm for 1 ms. This results in electrofusion of these cells with a fusion yield of around 5%. The operation with individual cell pairs, the appreciable efficiency and the potential to operate in high-throughput (up to 500 cells sec(−1)) makes the microdroplet fusion technology a promising platform for cell electrofusion, which has the potential to compete with the conventional methods. Besides, this platform is not restricted to cell fusion but is also applicable to various other cell-based assays such as single cell analysis and differentiation assays. |
format | Online Article Text |
id | pubmed-5829161 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-58291612018-03-01 Electrofusion of single cells in picoliter droplets Schoeman, Rogier M. van den Beld, Wesley T. E. Kemna, Evelien W. M. Wolbers, Floor Eijkel, Jan C. T. van den Berg, Albert Sci Rep Article We present a microfluidic chip that enables electrofusion of cells in microdroplets, with exchange of nuclear components. It is shown, to our knowledge for the first time, electrofusion of two HL60 cells, inside a microdroplet. This is the crucial intermediate step for controlled hybridoma formation where a B cell is electrofused with a myeloma cell. We use a microfluidic device consisting of a microchannel structure in PDMS bonded to a glass substrate through which droplets with two differently stained HL60 cells are transported. An array of six recessed platinum electrode pairs is used for electrofusion. When applying six voltage pulses of 2–3 V, the membrane electrical field is about 1 MV/cm for 1 ms. This results in electrofusion of these cells with a fusion yield of around 5%. The operation with individual cell pairs, the appreciable efficiency and the potential to operate in high-throughput (up to 500 cells sec(−1)) makes the microdroplet fusion technology a promising platform for cell electrofusion, which has the potential to compete with the conventional methods. Besides, this platform is not restricted to cell fusion but is also applicable to various other cell-based assays such as single cell analysis and differentiation assays. Nature Publishing Group UK 2018-02-27 /pmc/articles/PMC5829161/ /pubmed/29487332 http://dx.doi.org/10.1038/s41598-018-21993-8 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 Schoeman, Rogier M. van den Beld, Wesley T. E. Kemna, Evelien W. M. Wolbers, Floor Eijkel, Jan C. T. van den Berg, Albert Electrofusion of single cells in picoliter droplets |
title | Electrofusion of single cells in picoliter droplets |
title_full | Electrofusion of single cells in picoliter droplets |
title_fullStr | Electrofusion of single cells in picoliter droplets |
title_full_unstemmed | Electrofusion of single cells in picoliter droplets |
title_short | Electrofusion of single cells in picoliter droplets |
title_sort | electrofusion of single cells in picoliter droplets |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5829161/ https://www.ncbi.nlm.nih.gov/pubmed/29487332 http://dx.doi.org/10.1038/s41598-018-21993-8 |
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