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Flatbed epi relief-contrast cellular monitoring system for stable cell culture
Consistent cell preparation is a fundamental preliminary step for understanding complex cellular mechanisms in various cell-based research fields, including basic cell biology, cancer research, and tissue engineering. However, certain elusive factors, such as cellular de-differentiation and contamin...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5432522/ https://www.ncbi.nlm.nih.gov/pubmed/28507330 http://dx.doi.org/10.1038/s41598-017-02001-x |
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author | Osaki, Tatsuya Kageyama, Tatsuto Shimazu, Yuka Mysnikova, Dina Takahashi, Shintaro Takimoto, Shinichi Fukuda, Junji |
author_facet | Osaki, Tatsuya Kageyama, Tatsuto Shimazu, Yuka Mysnikova, Dina Takahashi, Shintaro Takimoto, Shinichi Fukuda, Junji |
author_sort | Osaki, Tatsuya |
collection | PubMed |
description | Consistent cell preparation is a fundamental preliminary step for understanding complex cellular mechanisms in various cell-based research fields, including basic cell biology, cancer research, and tissue engineering. However, certain elusive factors, such as cellular de-differentiation and contamination with mycoplasma or other types of cells, have compromised the reproducibility and reliability of cell-based approaches. Here, we propose an epi relief-contrast cellular monitoring system (eRC-CMS) that allows images of cells in a typical culture plate to be acquired, stored, and analysed for daily cell quality control. Due to its full flatbed nature and automated system, cells placed at any location on the stage can be analysed without special attention. Using this system, changes in the size, circularity, and proliferation of endothelial cells in subculture were recorded. Analyses of images of ~9,930,000 individual cells revealed that the growth activity and cell circularity in subcultures were closely correlated with their angiogenic activity in a subsequent hydrogel assay, demonstrating that eRC-CMS is useful for assessing cell quality in advance. We further demonstrated that eRC-CMS was feasible for the imaging of neurite elongation and spheroid formation. This system may provide a robust and versatile approach for daily cell preparation to facilitate reliable and reproducible cell-based studies. |
format | Online Article Text |
id | pubmed-5432522 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-54325222017-05-17 Flatbed epi relief-contrast cellular monitoring system for stable cell culture Osaki, Tatsuya Kageyama, Tatsuto Shimazu, Yuka Mysnikova, Dina Takahashi, Shintaro Takimoto, Shinichi Fukuda, Junji Sci Rep Article Consistent cell preparation is a fundamental preliminary step for understanding complex cellular mechanisms in various cell-based research fields, including basic cell biology, cancer research, and tissue engineering. However, certain elusive factors, such as cellular de-differentiation and contamination with mycoplasma or other types of cells, have compromised the reproducibility and reliability of cell-based approaches. Here, we propose an epi relief-contrast cellular monitoring system (eRC-CMS) that allows images of cells in a typical culture plate to be acquired, stored, and analysed for daily cell quality control. Due to its full flatbed nature and automated system, cells placed at any location on the stage can be analysed without special attention. Using this system, changes in the size, circularity, and proliferation of endothelial cells in subculture were recorded. Analyses of images of ~9,930,000 individual cells revealed that the growth activity and cell circularity in subcultures were closely correlated with their angiogenic activity in a subsequent hydrogel assay, demonstrating that eRC-CMS is useful for assessing cell quality in advance. We further demonstrated that eRC-CMS was feasible for the imaging of neurite elongation and spheroid formation. This system may provide a robust and versatile approach for daily cell preparation to facilitate reliable and reproducible cell-based studies. Nature Publishing Group UK 2017-05-15 /pmc/articles/PMC5432522/ /pubmed/28507330 http://dx.doi.org/10.1038/s41598-017-02001-x Text en © The Author(s) 2017 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 Osaki, Tatsuya Kageyama, Tatsuto Shimazu, Yuka Mysnikova, Dina Takahashi, Shintaro Takimoto, Shinichi Fukuda, Junji Flatbed epi relief-contrast cellular monitoring system for stable cell culture |
title | Flatbed epi relief-contrast cellular monitoring system for stable cell culture |
title_full | Flatbed epi relief-contrast cellular monitoring system for stable cell culture |
title_fullStr | Flatbed epi relief-contrast cellular monitoring system for stable cell culture |
title_full_unstemmed | Flatbed epi relief-contrast cellular monitoring system for stable cell culture |
title_short | Flatbed epi relief-contrast cellular monitoring system for stable cell culture |
title_sort | flatbed epi relief-contrast cellular monitoring system for stable cell culture |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5432522/ https://www.ncbi.nlm.nih.gov/pubmed/28507330 http://dx.doi.org/10.1038/s41598-017-02001-x |
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