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Integrating impedance-based growth-rate monitoring into a microfluidic cell culture platform for live-cell microscopy
Growth rate is a widely studied parameter for various cell-based biological studies. Growth rates of cell populations can be monitored in chemostats and micro-chemostats, where nutrients are continuously replenished. Here, we present an integrated microfluidic platform that enables long-term culturi...
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/PMC6220194/ https://www.ncbi.nlm.nih.gov/pubmed/31057898 http://dx.doi.org/10.1038/s41378-018-0006-5 |
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author | Chawla, Ketki Bürgel, Sebastian C. Schmidt, Gregor W. Kaltenbach, Hans-Michael Rudolf, Fabian Frey, Olivier Hierlemann, Andreas |
author_facet | Chawla, Ketki Bürgel, Sebastian C. Schmidt, Gregor W. Kaltenbach, Hans-Michael Rudolf, Fabian Frey, Olivier Hierlemann, Andreas |
author_sort | Chawla, Ketki |
collection | PubMed |
description | Growth rate is a widely studied parameter for various cell-based biological studies. Growth rates of cell populations can be monitored in chemostats and micro-chemostats, where nutrients are continuously replenished. Here, we present an integrated microfluidic platform that enables long-term culturing of non-adherent cells as well as parallel and mutually independent continuous monitoring of (i) growth rates of cells by means of impedance measurements and of (ii) specific other cellular events by means of high-resolution optical or fluorescence microscopy. Yeast colonies were grown in a monolayer under culturing pads, which enabled high-resolution microscopy, as all cells were in the same focal plane. Upon cell growth and division, cells leaving the culturing area passed over a pair of electrodes and were counted through impedance measurements. The impedance data could then be used to directly determine the growth rates of the cells in the culturing area. The integration of multiple culturing chambers with sensing electrodes enabled multiplexed long-term monitoring of growth rates of different yeast strains in parallel. As a demonstration, we modulated the growth rates of engineered yeast strains using calcium. The results indicated that impedance measurements provide a label-free readout method to continuously monitor the changes in the growth rates of the cells without compromising high-resolution optical imaging of single cells. |
format | Online Article Text |
id | pubmed-6220194 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-62201942019-05-03 Integrating impedance-based growth-rate monitoring into a microfluidic cell culture platform for live-cell microscopy Chawla, Ketki Bürgel, Sebastian C. Schmidt, Gregor W. Kaltenbach, Hans-Michael Rudolf, Fabian Frey, Olivier Hierlemann, Andreas Microsyst Nanoeng Article Growth rate is a widely studied parameter for various cell-based biological studies. Growth rates of cell populations can be monitored in chemostats and micro-chemostats, where nutrients are continuously replenished. Here, we present an integrated microfluidic platform that enables long-term culturing of non-adherent cells as well as parallel and mutually independent continuous monitoring of (i) growth rates of cells by means of impedance measurements and of (ii) specific other cellular events by means of high-resolution optical or fluorescence microscopy. Yeast colonies were grown in a monolayer under culturing pads, which enabled high-resolution microscopy, as all cells were in the same focal plane. Upon cell growth and division, cells leaving the culturing area passed over a pair of electrodes and were counted through impedance measurements. The impedance data could then be used to directly determine the growth rates of the cells in the culturing area. The integration of multiple culturing chambers with sensing electrodes enabled multiplexed long-term monitoring of growth rates of different yeast strains in parallel. As a demonstration, we modulated the growth rates of engineered yeast strains using calcium. The results indicated that impedance measurements provide a label-free readout method to continuously monitor the changes in the growth rates of the cells without compromising high-resolution optical imaging of single cells. Nature Publishing Group UK 2018-05-24 /pmc/articles/PMC6220194/ /pubmed/31057898 http://dx.doi.org/10.1038/s41378-018-0006-5 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 Chawla, Ketki Bürgel, Sebastian C. Schmidt, Gregor W. Kaltenbach, Hans-Michael Rudolf, Fabian Frey, Olivier Hierlemann, Andreas Integrating impedance-based growth-rate monitoring into a microfluidic cell culture platform for live-cell microscopy |
title | Integrating impedance-based growth-rate monitoring into a microfluidic cell culture platform for live-cell microscopy |
title_full | Integrating impedance-based growth-rate monitoring into a microfluidic cell culture platform for live-cell microscopy |
title_fullStr | Integrating impedance-based growth-rate monitoring into a microfluidic cell culture platform for live-cell microscopy |
title_full_unstemmed | Integrating impedance-based growth-rate monitoring into a microfluidic cell culture platform for live-cell microscopy |
title_short | Integrating impedance-based growth-rate monitoring into a microfluidic cell culture platform for live-cell microscopy |
title_sort | integrating impedance-based growth-rate monitoring into a microfluidic cell culture platform for live-cell microscopy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6220194/ https://www.ncbi.nlm.nih.gov/pubmed/31057898 http://dx.doi.org/10.1038/s41378-018-0006-5 |
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