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Compact automated culture machine for human induced pluripotent stem cell maintenance and differentiation

The technologies used to generate human induced pluripotent stem cell (iPSC) from somatic cells potentially enable the wide application of iPSC-derived differentiated cells in industrial research fields as a replacement for animals. However, as highly trained individuals are required to obtain repro...

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Autores principales: Bando, Kazunori, Yamashita, Hiromi, Tsumori, Motomu, Minoura, Hayase, Okumura, Koji, Hattori, Fumiyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9744792/
https://www.ncbi.nlm.nih.gov/pubmed/36524054
http://dx.doi.org/10.3389/fbioe.2022.1074990
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author Bando, Kazunori
Yamashita, Hiromi
Tsumori, Motomu
Minoura, Hayase
Okumura, Koji
Hattori, Fumiyuki
author_facet Bando, Kazunori
Yamashita, Hiromi
Tsumori, Motomu
Minoura, Hayase
Okumura, Koji
Hattori, Fumiyuki
author_sort Bando, Kazunori
collection PubMed
description The technologies used to generate human induced pluripotent stem cell (iPSC) from somatic cells potentially enable the wide application of iPSC-derived differentiated cells in industrial research fields as a replacement for animals. However, as highly trained individuals are required to obtain reproducible results, this approach has limited social implementation. In the research field of iPSC, it is believed that documentable information is not enough for reproducing the quality of the differentiated cells. Therefore, automated culture machines for cell processing should make the starting of iPSC-using researches easier. We developed a programmable all-in-one automated culture machine, with dense and compact constitution that fits within a normal biosafety cabinet (200 mm wide, 233 mm height, and 110 mm depth). This instrument was fabricated using novel x-y-z-axes-rail-system, such as an overhead traveling crane, in a factory, which served as the main handling machinery. This machine enabled stable and efficient expansion of human iPSC under the feeder-free condition, without karyotype alterations, and simultaneously differentiated the cells into various cell types, including cardiomyocytes, hepatocytes, neural progenitors, and keratinocytes. Overall, this machine would facilitate the social implementation of human pluripotent stem cells and contribute to the accumulation of sharable knowledge for the standardization of the entire handling processes of iPSC in pharmaceutical, food, and cosmetic research.
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spelling pubmed-97447922022-12-14 Compact automated culture machine for human induced pluripotent stem cell maintenance and differentiation Bando, Kazunori Yamashita, Hiromi Tsumori, Motomu Minoura, Hayase Okumura, Koji Hattori, Fumiyuki Front Bioeng Biotechnol Bioengineering and Biotechnology The technologies used to generate human induced pluripotent stem cell (iPSC) from somatic cells potentially enable the wide application of iPSC-derived differentiated cells in industrial research fields as a replacement for animals. However, as highly trained individuals are required to obtain reproducible results, this approach has limited social implementation. In the research field of iPSC, it is believed that documentable information is not enough for reproducing the quality of the differentiated cells. Therefore, automated culture machines for cell processing should make the starting of iPSC-using researches easier. We developed a programmable all-in-one automated culture machine, with dense and compact constitution that fits within a normal biosafety cabinet (200 mm wide, 233 mm height, and 110 mm depth). This instrument was fabricated using novel x-y-z-axes-rail-system, such as an overhead traveling crane, in a factory, which served as the main handling machinery. This machine enabled stable and efficient expansion of human iPSC under the feeder-free condition, without karyotype alterations, and simultaneously differentiated the cells into various cell types, including cardiomyocytes, hepatocytes, neural progenitors, and keratinocytes. Overall, this machine would facilitate the social implementation of human pluripotent stem cells and contribute to the accumulation of sharable knowledge for the standardization of the entire handling processes of iPSC in pharmaceutical, food, and cosmetic research. Frontiers Media S.A. 2022-11-29 /pmc/articles/PMC9744792/ /pubmed/36524054 http://dx.doi.org/10.3389/fbioe.2022.1074990 Text en Copyright © 2022 Bando, Yamashita, Tsumori, Minoura, Okumura and Hattori. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Bioengineering and Biotechnology
Bando, Kazunori
Yamashita, Hiromi
Tsumori, Motomu
Minoura, Hayase
Okumura, Koji
Hattori, Fumiyuki
Compact automated culture machine for human induced pluripotent stem cell maintenance and differentiation
title Compact automated culture machine for human induced pluripotent stem cell maintenance and differentiation
title_full Compact automated culture machine for human induced pluripotent stem cell maintenance and differentiation
title_fullStr Compact automated culture machine for human induced pluripotent stem cell maintenance and differentiation
title_full_unstemmed Compact automated culture machine for human induced pluripotent stem cell maintenance and differentiation
title_short Compact automated culture machine for human induced pluripotent stem cell maintenance and differentiation
title_sort compact automated culture machine for human induced pluripotent stem cell maintenance and differentiation
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9744792/
https://www.ncbi.nlm.nih.gov/pubmed/36524054
http://dx.doi.org/10.3389/fbioe.2022.1074990
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