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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...

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Autores principales: Kinoshita, Koji, Munesue, Takuya, Toki, Fujio, Isshiki, Masaharu, Higashiyama, Shigeki, Barrandon, Yann, Nishimura, Emi K., Yanagihara, Yoshio, Nanba, Daisuke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
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.
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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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