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Automated collective motion analysis validates human keratinocyte stem cell cultures
Identification and quality assurance of stem cells cultured in heterogeneous cell populations are indispensable for successful stem cell therapy. Here we present an image-processing pipeline for automated identification and quality assessment of human keratinocyte stem cells. When cultivated under a...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6904747/ https://www.ncbi.nlm.nih.gov/pubmed/31822757 http://dx.doi.org/10.1038/s41598-019-55279-4 |
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author | Kinoshita, Koji Munesue, Takuya Toki, Fujio Isshiki, Masaharu Higashiyama, Shigeki Barrandon, Yann Nishimura, Emi K. Yanagihara, Yoshio Nanba, Daisuke |
author_facet | Kinoshita, Koji Munesue, Takuya Toki, Fujio Isshiki, Masaharu Higashiyama, Shigeki Barrandon, Yann Nishimura, Emi K. Yanagihara, Yoshio Nanba, Daisuke |
author_sort | Kinoshita, Koji |
collection | PubMed |
description | Identification and quality assurance of stem cells cultured in heterogeneous cell populations are indispensable for successful stem cell therapy. Here we present an image-processing pipeline for automated identification and quality assessment of human keratinocyte stem cells. When cultivated under appropriate conditions, human epidermal keratinocyte stem cells give rise to colonies and exhibit higher locomotive capacity as well as significant proliferative potential. Image processing and kernel density estimation were used to automatically extract the area of keratinocyte colonies from phase-contrast images of cultures containing feeder cells. The DeepFlow algorithm was then used to calculate locomotion speed of the colony area by analyzing serial images. This image-processing pipeline successfully identified keratinocyte stem cell colonies by measuring cell locomotion speed, and also assessed the effect of oligotrophic culture conditions and chemical inhibitors on keratinocyte behavior. Therefore, this study provides automated procedures for image-based quality control of stem cell cultures and high-throughput screening of small molecules targeting stem cells. |
format | Online Article Text |
id | pubmed-6904747 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69047472019-12-13 Automated collective motion analysis validates human keratinocyte stem cell cultures Kinoshita, Koji Munesue, Takuya Toki, Fujio Isshiki, Masaharu Higashiyama, Shigeki Barrandon, Yann Nishimura, Emi K. Yanagihara, Yoshio Nanba, Daisuke Sci Rep Article Identification and quality assurance of stem cells cultured in heterogeneous cell populations are indispensable for successful stem cell therapy. Here we present an image-processing pipeline for automated identification and quality assessment of human keratinocyte stem cells. When cultivated under appropriate conditions, human epidermal keratinocyte stem cells give rise to colonies and exhibit higher locomotive capacity as well as significant proliferative potential. Image processing and kernel density estimation were used to automatically extract the area of keratinocyte colonies from phase-contrast images of cultures containing feeder cells. The DeepFlow algorithm was then used to calculate locomotion speed of the colony area by analyzing serial images. This image-processing pipeline successfully identified keratinocyte stem cell colonies by measuring cell locomotion speed, and also assessed the effect of oligotrophic culture conditions and chemical inhibitors on keratinocyte behavior. Therefore, this study provides automated procedures for image-based quality control of stem cell cultures and high-throughput screening of small molecules targeting stem cells. Nature Publishing Group UK 2019-12-10 /pmc/articles/PMC6904747/ /pubmed/31822757 http://dx.doi.org/10.1038/s41598-019-55279-4 Text en © The Author(s) 2019 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 Kinoshita, Koji Munesue, Takuya Toki, Fujio Isshiki, Masaharu Higashiyama, Shigeki Barrandon, Yann Nishimura, Emi K. Yanagihara, Yoshio Nanba, Daisuke Automated collective motion analysis validates human keratinocyte stem cell cultures |
title | Automated collective motion analysis validates human keratinocyte stem cell cultures |
title_full | Automated collective motion analysis validates human keratinocyte stem cell cultures |
title_fullStr | Automated collective motion analysis validates human keratinocyte stem cell cultures |
title_full_unstemmed | Automated collective motion analysis validates human keratinocyte stem cell cultures |
title_short | Automated collective motion analysis validates human keratinocyte stem cell cultures |
title_sort | automated collective motion analysis validates human keratinocyte stem cell cultures |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6904747/ https://www.ncbi.nlm.nih.gov/pubmed/31822757 http://dx.doi.org/10.1038/s41598-019-55279-4 |
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