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Single-neuronal cell culture and monitoring platform using a fully transparent microfluidic DEP device
Dielectrophoresis using multi-electrode arrays allows a non-invasive interface with biological cells for long-term monitoring of electrophysiological parameters as well as a label-free and non-destructive technique for neuronal cell manipulation. However, experiments for neuronal cell manipulation u...
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/PMC6123457/ https://www.ncbi.nlm.nih.gov/pubmed/30181589 http://dx.doi.org/10.1038/s41598-018-31576-2 |
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author | Kim, Hyungsoo Lee, In-Kyu Taylor, Kendra Richters, Karl Baek, Dong-Hyun Ryu, Jae Ha Cho, Sang June Jung, Yei Hwan Park, Dong-Wook Novello, Joseph Bong, Jihye Suminski, Aaron J. Dingle, Aaron M. Blick, Robert H. Williams, Justin C. Dent, Erik W. Ma, Zhenqiang |
author_facet | Kim, Hyungsoo Lee, In-Kyu Taylor, Kendra Richters, Karl Baek, Dong-Hyun Ryu, Jae Ha Cho, Sang June Jung, Yei Hwan Park, Dong-Wook Novello, Joseph Bong, Jihye Suminski, Aaron J. Dingle, Aaron M. Blick, Robert H. Williams, Justin C. Dent, Erik W. Ma, Zhenqiang |
author_sort | Kim, Hyungsoo |
collection | PubMed |
description | Dielectrophoresis using multi-electrode arrays allows a non-invasive interface with biological cells for long-term monitoring of electrophysiological parameters as well as a label-free and non-destructive technique for neuronal cell manipulation. However, experiments for neuronal cell manipulation utilizing dielectrophoresis have been constrained because dielectrophoresis devices generally function outside of the controlled environment (i.e. incubator) during the cell manipulation process, which is problematic because neurons are highly susceptible to the properties of the physiochemical environment. Furthermore, the conventional multi-electrode arrays designed to generate dielectrophoretic force are often fabricated with non-transparent materials that confound live-cell imaging. Here we present an advanced single-neuronal cell culture and monitoring platform using a fully transparent microfluidic dielectrophoresis device for the unabated monitoring of neuronal cell development and function. The device is mounted inside a sealed incubation chamber to ensure improved homeostatic conditions and reduced contamination risk. Consequently, we successfully trap and culture single neurons on a desired location and monitor their growth process over a week. The proposed single-neuronal cell culture and monitoring platform not only has significant potential to realize an in vitro ordered neuronal network, but also offers a useful tool for a wide range of neurological research and electrophysiological studies of neuronal networks. |
format | Online Article Text |
id | pubmed-6123457 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61234572018-09-10 Single-neuronal cell culture and monitoring platform using a fully transparent microfluidic DEP device Kim, Hyungsoo Lee, In-Kyu Taylor, Kendra Richters, Karl Baek, Dong-Hyun Ryu, Jae Ha Cho, Sang June Jung, Yei Hwan Park, Dong-Wook Novello, Joseph Bong, Jihye Suminski, Aaron J. Dingle, Aaron M. Blick, Robert H. Williams, Justin C. Dent, Erik W. Ma, Zhenqiang Sci Rep Article Dielectrophoresis using multi-electrode arrays allows a non-invasive interface with biological cells for long-term monitoring of electrophysiological parameters as well as a label-free and non-destructive technique for neuronal cell manipulation. However, experiments for neuronal cell manipulation utilizing dielectrophoresis have been constrained because dielectrophoresis devices generally function outside of the controlled environment (i.e. incubator) during the cell manipulation process, which is problematic because neurons are highly susceptible to the properties of the physiochemical environment. Furthermore, the conventional multi-electrode arrays designed to generate dielectrophoretic force are often fabricated with non-transparent materials that confound live-cell imaging. Here we present an advanced single-neuronal cell culture and monitoring platform using a fully transparent microfluidic dielectrophoresis device for the unabated monitoring of neuronal cell development and function. The device is mounted inside a sealed incubation chamber to ensure improved homeostatic conditions and reduced contamination risk. Consequently, we successfully trap and culture single neurons on a desired location and monitor their growth process over a week. The proposed single-neuronal cell culture and monitoring platform not only has significant potential to realize an in vitro ordered neuronal network, but also offers a useful tool for a wide range of neurological research and electrophysiological studies of neuronal networks. Nature Publishing Group UK 2018-09-04 /pmc/articles/PMC6123457/ /pubmed/30181589 http://dx.doi.org/10.1038/s41598-018-31576-2 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 Kim, Hyungsoo Lee, In-Kyu Taylor, Kendra Richters, Karl Baek, Dong-Hyun Ryu, Jae Ha Cho, Sang June Jung, Yei Hwan Park, Dong-Wook Novello, Joseph Bong, Jihye Suminski, Aaron J. Dingle, Aaron M. Blick, Robert H. Williams, Justin C. Dent, Erik W. Ma, Zhenqiang Single-neuronal cell culture and monitoring platform using a fully transparent microfluidic DEP device |
title | Single-neuronal cell culture and monitoring platform using a fully transparent microfluidic DEP device |
title_full | Single-neuronal cell culture and monitoring platform using a fully transparent microfluidic DEP device |
title_fullStr | Single-neuronal cell culture and monitoring platform using a fully transparent microfluidic DEP device |
title_full_unstemmed | Single-neuronal cell culture and monitoring platform using a fully transparent microfluidic DEP device |
title_short | Single-neuronal cell culture and monitoring platform using a fully transparent microfluidic DEP device |
title_sort | single-neuronal cell culture and monitoring platform using a fully transparent microfluidic dep device |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6123457/ https://www.ncbi.nlm.nih.gov/pubmed/30181589 http://dx.doi.org/10.1038/s41598-018-31576-2 |
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