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Time-lapse electrical impedance spectroscopy for monitoring the cell cycle of single immobilized S. pombe cells
As a complement and alternative to optical methods, wide-band electrical impedance spectroscopy (EIS) enables multi-parameter, label-free and real-time detection of cellular and subcellular features. We report on a microfluidics-based system designed to reliably capture single rod-shaped Schizosacch...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4660434/ https://www.ncbi.nlm.nih.gov/pubmed/26608589 http://dx.doi.org/10.1038/srep17180 |
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author | Zhu, Zhen Frey, Olivier Haandbaek, Niels Franke, Felix Rudolf, Fabian Hierlemann, Andreas |
author_facet | Zhu, Zhen Frey, Olivier Haandbaek, Niels Franke, Felix Rudolf, Fabian Hierlemann, Andreas |
author_sort | Zhu, Zhen |
collection | PubMed |
description | As a complement and alternative to optical methods, wide-band electrical impedance spectroscopy (EIS) enables multi-parameter, label-free and real-time detection of cellular and subcellular features. We report on a microfluidics-based system designed to reliably capture single rod-shaped Schizosaccharomyces pombe cells by applying suction through orifices in a channel wall. The system enables subsequent culturing of immobilized cells in an upright position, while dynamic changes in cell-cycle state and morphology were continuously monitored through EIS over a broad frequency range. Besides measuring cell growth, clear impedance signals for nuclear division have been obtained. The EIS system has been characterized with respect to sensitivity and detection limits. The spatial resolution in measuring cell length was 0.25 μm, which corresponds to approximately a 5-min interval of cell growth under standard conditions. The comprehensive impedance data sets were also used to determine the occurrence of nuclear division and cytokinesis. The obtained results have been validated through concurrent confocal imaging and plausibilized through comparison with finite-element modeling data. The possibility to monitor cellular and intracellular features of single S. pombe cells during the cell cycle at high spatiotemporal resolution renders the presented microfluidics-based EIS system a suitable tool for dynamic single-cell investigations. |
format | Online Article Text |
id | pubmed-4660434 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46604342015-12-02 Time-lapse electrical impedance spectroscopy for monitoring the cell cycle of single immobilized S. pombe cells Zhu, Zhen Frey, Olivier Haandbaek, Niels Franke, Felix Rudolf, Fabian Hierlemann, Andreas Sci Rep Article As a complement and alternative to optical methods, wide-band electrical impedance spectroscopy (EIS) enables multi-parameter, label-free and real-time detection of cellular and subcellular features. We report on a microfluidics-based system designed to reliably capture single rod-shaped Schizosaccharomyces pombe cells by applying suction through orifices in a channel wall. The system enables subsequent culturing of immobilized cells in an upright position, while dynamic changes in cell-cycle state and morphology were continuously monitored through EIS over a broad frequency range. Besides measuring cell growth, clear impedance signals for nuclear division have been obtained. The EIS system has been characterized with respect to sensitivity and detection limits. The spatial resolution in measuring cell length was 0.25 μm, which corresponds to approximately a 5-min interval of cell growth under standard conditions. The comprehensive impedance data sets were also used to determine the occurrence of nuclear division and cytokinesis. The obtained results have been validated through concurrent confocal imaging and plausibilized through comparison with finite-element modeling data. The possibility to monitor cellular and intracellular features of single S. pombe cells during the cell cycle at high spatiotemporal resolution renders the presented microfluidics-based EIS system a suitable tool for dynamic single-cell investigations. Nature Publishing Group 2015-11-26 /pmc/articles/PMC4660434/ /pubmed/26608589 http://dx.doi.org/10.1038/srep17180 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Zhu, Zhen Frey, Olivier Haandbaek, Niels Franke, Felix Rudolf, Fabian Hierlemann, Andreas Time-lapse electrical impedance spectroscopy for monitoring the cell cycle of single immobilized S. pombe cells |
title | Time-lapse electrical impedance spectroscopy for monitoring the cell cycle of single
immobilized S. pombe cells |
title_full | Time-lapse electrical impedance spectroscopy for monitoring the cell cycle of single
immobilized S. pombe cells |
title_fullStr | Time-lapse electrical impedance spectroscopy for monitoring the cell cycle of single
immobilized S. pombe cells |
title_full_unstemmed | Time-lapse electrical impedance spectroscopy for monitoring the cell cycle of single
immobilized S. pombe cells |
title_short | Time-lapse electrical impedance spectroscopy for monitoring the cell cycle of single
immobilized S. pombe cells |
title_sort | time-lapse electrical impedance spectroscopy for monitoring the cell cycle of single
immobilized s. pombe cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4660434/ https://www.ncbi.nlm.nih.gov/pubmed/26608589 http://dx.doi.org/10.1038/srep17180 |
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