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Fabrication Scaffold with High Dimensional Control for Spheroids with Undifferentiated iPS Cell Properties
Spheroids are expected to aid the establishment of an in vitro-based cell culture system that can realistically reproduce cellular dynamics in vivo. We developed a fluoropolymer scaffold with an extracellular matrix (ECM) dot array and confirmed the possibility of mass-producing spheroids with unifo...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9857117/ https://www.ncbi.nlm.nih.gov/pubmed/36672213 http://dx.doi.org/10.3390/cells12020278 |
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author | Togo, Hidetaka Terada, Kento Ujitsugu, Akira Hirose, Yudai Takeuchi, Hiroki Kusunoki, Masanobu |
author_facet | Togo, Hidetaka Terada, Kento Ujitsugu, Akira Hirose, Yudai Takeuchi, Hiroki Kusunoki, Masanobu |
author_sort | Togo, Hidetaka |
collection | PubMed |
description | Spheroids are expected to aid the establishment of an in vitro-based cell culture system that can realistically reproduce cellular dynamics in vivo. We developed a fluoropolymer scaffold with an extracellular matrix (ECM) dot array and confirmed the possibility of mass-producing spheroids with uniform dimensions. Controlling the quality of ECM dots is important as it ensures spheroid uniformity, but issues such as pattern deviation and ECM drying persist in the conventional microstamping method. In this study, these problems were overcome via ECM dot printing using a resin mask with dot-patterned holes. For dot diameters of φ 300 μm, 400 μm, and 600 μm, the average spheroid diameters of human iPS cells (hiPSCs) were φ 260.8 μm, 292.4 μm, and 330.7 μm, respectively. The standard deviation when each average was normalized to 100 was 14.1%. A high throughput of 89.9% for colony formation rate to the number of dots and 89.3% for spheroid collection rate was achieved. The cells proliferated on ECM dots, and the colonies could be naturally detached from the scaffold without the use of enzymes, so there was almost no stimulation of the cells. Thus, the undifferentiated nature of hiPSCs was maintained until day 4. Therefore, this method is expected to be useful in drug discovery and regenerative medicine. |
format | Online Article Text |
id | pubmed-9857117 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-98571172023-01-21 Fabrication Scaffold with High Dimensional Control for Spheroids with Undifferentiated iPS Cell Properties Togo, Hidetaka Terada, Kento Ujitsugu, Akira Hirose, Yudai Takeuchi, Hiroki Kusunoki, Masanobu Cells Article Spheroids are expected to aid the establishment of an in vitro-based cell culture system that can realistically reproduce cellular dynamics in vivo. We developed a fluoropolymer scaffold with an extracellular matrix (ECM) dot array and confirmed the possibility of mass-producing spheroids with uniform dimensions. Controlling the quality of ECM dots is important as it ensures spheroid uniformity, but issues such as pattern deviation and ECM drying persist in the conventional microstamping method. In this study, these problems were overcome via ECM dot printing using a resin mask with dot-patterned holes. For dot diameters of φ 300 μm, 400 μm, and 600 μm, the average spheroid diameters of human iPS cells (hiPSCs) were φ 260.8 μm, 292.4 μm, and 330.7 μm, respectively. The standard deviation when each average was normalized to 100 was 14.1%. A high throughput of 89.9% for colony formation rate to the number of dots and 89.3% for spheroid collection rate was achieved. The cells proliferated on ECM dots, and the colonies could be naturally detached from the scaffold without the use of enzymes, so there was almost no stimulation of the cells. Thus, the undifferentiated nature of hiPSCs was maintained until day 4. Therefore, this method is expected to be useful in drug discovery and regenerative medicine. MDPI 2023-01-11 /pmc/articles/PMC9857117/ /pubmed/36672213 http://dx.doi.org/10.3390/cells12020278 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Togo, Hidetaka Terada, Kento Ujitsugu, Akira Hirose, Yudai Takeuchi, Hiroki Kusunoki, Masanobu Fabrication Scaffold with High Dimensional Control for Spheroids with Undifferentiated iPS Cell Properties |
title | Fabrication Scaffold with High Dimensional Control for Spheroids with Undifferentiated iPS Cell Properties |
title_full | Fabrication Scaffold with High Dimensional Control for Spheroids with Undifferentiated iPS Cell Properties |
title_fullStr | Fabrication Scaffold with High Dimensional Control for Spheroids with Undifferentiated iPS Cell Properties |
title_full_unstemmed | Fabrication Scaffold with High Dimensional Control for Spheroids with Undifferentiated iPS Cell Properties |
title_short | Fabrication Scaffold with High Dimensional Control for Spheroids with Undifferentiated iPS Cell Properties |
title_sort | fabrication scaffold with high dimensional control for spheroids with undifferentiated ips cell properties |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9857117/ https://www.ncbi.nlm.nih.gov/pubmed/36672213 http://dx.doi.org/10.3390/cells12020278 |
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