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A Microcavity Array-Based 4D Cell Culture Platform
(1) Background: We describe a 4D cell culture platform with which we tried to detect and to characterize migration dynamics of single hematopoietic stem cells in polymer film microcavity arrays integrated into a microtiter plate. (2) Methods: The system was set up with CD34-expressing KG-1a cells as...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6631836/ https://www.ncbi.nlm.nih.gov/pubmed/31159244 http://dx.doi.org/10.3390/bioengineering6020050 |
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author | Nies, Cordula Rubner, Tobias Lorig, Hanna Colditz, Vera Seelmann, Helen Müller, Andreas Gottwald, Eric |
author_facet | Nies, Cordula Rubner, Tobias Lorig, Hanna Colditz, Vera Seelmann, Helen Müller, Andreas Gottwald, Eric |
author_sort | Nies, Cordula |
collection | PubMed |
description | (1) Background: We describe a 4D cell culture platform with which we tried to detect and to characterize migration dynamics of single hematopoietic stem cells in polymer film microcavity arrays integrated into a microtiter plate. (2) Methods: The system was set up with CD34-expressing KG-1a cells as a surrogate for hematopoietic stem cells. We then evaluated the system as an artificial hematopoietic stem cell niche model comprised of a co-culture of human hematopoietic stem cells from cord blood (cord blood CD34(+) cells, hHSCs) and human mesenchymal stromal cells (hMSCs) from bone marrow over a period of 21 days. We used a software-based cell detection method to count single hematopoietic stem cells (HSCs) in microcavities. (3) Results: It was possible to detect single HSCs and their migration behavior within single microcavities. The HSCs displayed a pronounced migration behavior with one population of CD34-expressing cells located at the bottom of the microcavities and one population located in the middle of the microcavities at day 14. However, at day 21 the two populations seemed to unite again so that no clear distinction between the two was possible anymore. (4) Conclusions: Single cell migration detection was possible but microscopy and flow cytometry delivered non-uniform data sets. Further optimization is currently being developed. |
format | Online Article Text |
id | pubmed-6631836 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-66318362019-08-19 A Microcavity Array-Based 4D Cell Culture Platform Nies, Cordula Rubner, Tobias Lorig, Hanna Colditz, Vera Seelmann, Helen Müller, Andreas Gottwald, Eric Bioengineering (Basel) Article (1) Background: We describe a 4D cell culture platform with which we tried to detect and to characterize migration dynamics of single hematopoietic stem cells in polymer film microcavity arrays integrated into a microtiter plate. (2) Methods: The system was set up with CD34-expressing KG-1a cells as a surrogate for hematopoietic stem cells. We then evaluated the system as an artificial hematopoietic stem cell niche model comprised of a co-culture of human hematopoietic stem cells from cord blood (cord blood CD34(+) cells, hHSCs) and human mesenchymal stromal cells (hMSCs) from bone marrow over a period of 21 days. We used a software-based cell detection method to count single hematopoietic stem cells (HSCs) in microcavities. (3) Results: It was possible to detect single HSCs and their migration behavior within single microcavities. The HSCs displayed a pronounced migration behavior with one population of CD34-expressing cells located at the bottom of the microcavities and one population located in the middle of the microcavities at day 14. However, at day 21 the two populations seemed to unite again so that no clear distinction between the two was possible anymore. (4) Conclusions: Single cell migration detection was possible but microscopy and flow cytometry delivered non-uniform data sets. Further optimization is currently being developed. MDPI 2019-05-31 /pmc/articles/PMC6631836/ /pubmed/31159244 http://dx.doi.org/10.3390/bioengineering6020050 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Nies, Cordula Rubner, Tobias Lorig, Hanna Colditz, Vera Seelmann, Helen Müller, Andreas Gottwald, Eric A Microcavity Array-Based 4D Cell Culture Platform |
title | A Microcavity Array-Based 4D Cell Culture Platform |
title_full | A Microcavity Array-Based 4D Cell Culture Platform |
title_fullStr | A Microcavity Array-Based 4D Cell Culture Platform |
title_full_unstemmed | A Microcavity Array-Based 4D Cell Culture Platform |
title_short | A Microcavity Array-Based 4D Cell Culture Platform |
title_sort | microcavity array-based 4d cell culture platform |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6631836/ https://www.ncbi.nlm.nih.gov/pubmed/31159244 http://dx.doi.org/10.3390/bioengineering6020050 |
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