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Rapid assay of stem cell functionality and potency using electric cell-substrate impedance sensing
Regenerative medicine studies using autologous bone marrow mononuclear cells (BM-MNCs) have shown improved clinical outcomes that correlate to in vitro BM-MNC invasive capacity. The current Boyden-chamber assay for testing invasive capacity is labor-intensive, provides only a single time point, and...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4594964/ https://www.ncbi.nlm.nih.gov/pubmed/26438432 http://dx.doi.org/10.1186/s13287-015-0182-2 |
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author | Rutten, Michael J. Laraway, Bryan Gregory, Cynthia R. Xie, Hua Renken, Christian Keese, Charles Gregory, Kenton W. |
author_facet | Rutten, Michael J. Laraway, Bryan Gregory, Cynthia R. Xie, Hua Renken, Christian Keese, Charles Gregory, Kenton W. |
author_sort | Rutten, Michael J. |
collection | PubMed |
description | Regenerative medicine studies using autologous bone marrow mononuclear cells (BM-MNCs) have shown improved clinical outcomes that correlate to in vitro BM-MNC invasive capacity. The current Boyden-chamber assay for testing invasive capacity is labor-intensive, provides only a single time point, and takes 36 hours to collect data and results, which is not practical from a clinical cell delivery perspective. To develop a rapid, sensitive and reproducible invasion assay, we employed Electric Cell-substrate Impedance Sensing (ECIS) technology. Chemokine-directed BM-MNC cell invasion across a Matrigel-coated Transwell filter was measurable within minutes using the ECIS system we developed. This ECIS-Transwell chamber system provides a rapid and sensitive test of stem and progenitor cell invasive capacity for evaluation of stem cell functionality to provide timely clinical data for selection of patients likely to realize clinical benefit in regenerative medicine treatments. This device could also supply robust unambiguous, reproducible and cost effective data as a potency assay for cell product release and regulatory strategies. |
format | Online Article Text |
id | pubmed-4594964 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-45949642015-10-07 Rapid assay of stem cell functionality and potency using electric cell-substrate impedance sensing Rutten, Michael J. Laraway, Bryan Gregory, Cynthia R. Xie, Hua Renken, Christian Keese, Charles Gregory, Kenton W. Stem Cell Res Ther Method Regenerative medicine studies using autologous bone marrow mononuclear cells (BM-MNCs) have shown improved clinical outcomes that correlate to in vitro BM-MNC invasive capacity. The current Boyden-chamber assay for testing invasive capacity is labor-intensive, provides only a single time point, and takes 36 hours to collect data and results, which is not practical from a clinical cell delivery perspective. To develop a rapid, sensitive and reproducible invasion assay, we employed Electric Cell-substrate Impedance Sensing (ECIS) technology. Chemokine-directed BM-MNC cell invasion across a Matrigel-coated Transwell filter was measurable within minutes using the ECIS system we developed. This ECIS-Transwell chamber system provides a rapid and sensitive test of stem and progenitor cell invasive capacity for evaluation of stem cell functionality to provide timely clinical data for selection of patients likely to realize clinical benefit in regenerative medicine treatments. This device could also supply robust unambiguous, reproducible and cost effective data as a potency assay for cell product release and regulatory strategies. BioMed Central 2015-10-05 /pmc/articles/PMC4594964/ /pubmed/26438432 http://dx.doi.org/10.1186/s13287-015-0182-2 Text en © Rutten et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Method Rutten, Michael J. Laraway, Bryan Gregory, Cynthia R. Xie, Hua Renken, Christian Keese, Charles Gregory, Kenton W. Rapid assay of stem cell functionality and potency using electric cell-substrate impedance sensing |
title | Rapid assay of stem cell functionality and potency using electric cell-substrate impedance sensing |
title_full | Rapid assay of stem cell functionality and potency using electric cell-substrate impedance sensing |
title_fullStr | Rapid assay of stem cell functionality and potency using electric cell-substrate impedance sensing |
title_full_unstemmed | Rapid assay of stem cell functionality and potency using electric cell-substrate impedance sensing |
title_short | Rapid assay of stem cell functionality and potency using electric cell-substrate impedance sensing |
title_sort | rapid assay of stem cell functionality and potency using electric cell-substrate impedance sensing |
topic | Method |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4594964/ https://www.ncbi.nlm.nih.gov/pubmed/26438432 http://dx.doi.org/10.1186/s13287-015-0182-2 |
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