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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...

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Autores principales: Nies, Cordula, Rubner, Tobias, Lorig, Hanna, Colditz, Vera, Seelmann, Helen, Müller, Andreas, Gottwald, Eric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
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.
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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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