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Gene expression analysis of human induced pluripotent stem cells cryopreserved by vitrification using StemCell Keep

In recent years, regenerative medicine research using human somatic and induced pluripotent stem cells has advanced considerably, promoting clinical applications. However, it is essential that these cells are cryopreserved safely and effectively. Most cryopreservation solution agents contain dimethy...

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Autores principales: Ota, Akemi, Hyon, Suong-Hyu, Sumi, Shoichiro, Matsumura, Kazuaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8605251/
https://www.ncbi.nlm.nih.gov/pubmed/34825070
http://dx.doi.org/10.1016/j.bbrep.2021.101172
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author Ota, Akemi
Hyon, Suong-Hyu
Sumi, Shoichiro
Matsumura, Kazuaki
author_facet Ota, Akemi
Hyon, Suong-Hyu
Sumi, Shoichiro
Matsumura, Kazuaki
author_sort Ota, Akemi
collection PubMed
description In recent years, regenerative medicine research using human somatic and induced pluripotent stem cells has advanced considerably, promoting clinical applications. However, it is essential that these cells are cryopreserved safely and effectively. Most cryopreservation solution agents contain dimethyl sulfoxide (DMSO), which exhibits strong toxicity and can potentially promote cell differentiation. Hence, it is important to explore substitutes for DMSO in cryoprotectant solutions. One such alternative is StemCell Keep (SCK), a DMSO-free solution that has been reported to effectively cryopreserve human induced pluripotent stem cells (hiPS cells). To clarify the effect of cryopreservation agents on cells, DNA microarray analysis is useful, as it can identify a large number of gene expression differences in cryopreserved cells, as well as functional increases in gene groups. In this study, we performed gene expression analysis of SCK-cryopreserved hiPS cells using a DNA microarray gene chip. The hiPS cells vitrified with SCK or DMSO-based vitrification solutions were thawed and cultured on Matrigel under feeder-free conditions, and RNA was extracted for DNA microarray analysis. Genes obtained from DNA microarray data were classified by the keywords of Gene Ontology Biological Process Term, and their relationships were analyzed using DAVID or the GeneMANIA database. SCK-cryopreserved hiPS cells expressed several anti-apoptotic genes, as well as genes related to cell adhesion or proliferation at levels that were nearly equivalent to those of non-frozen hiPS cells. Gene enrichment analysis with selected genes of SCK-cryopreserved hiPS cells whose expression differences were superior to those of DAP-cryopreserved showed strong interactions of negative regulation of apoptotic process, cell adhesion and positive regulation of cell proliferation in DAVID analysis. We demonstrated that SCK successfully maintained the key functions of hiPS cells, including anti-apoptosis, cell adhesion, and cell proliferation, during cryopreservation.
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spelling pubmed-86052512021-11-24 Gene expression analysis of human induced pluripotent stem cells cryopreserved by vitrification using StemCell Keep Ota, Akemi Hyon, Suong-Hyu Sumi, Shoichiro Matsumura, Kazuaki Biochem Biophys Rep Research Article In recent years, regenerative medicine research using human somatic and induced pluripotent stem cells has advanced considerably, promoting clinical applications. However, it is essential that these cells are cryopreserved safely and effectively. Most cryopreservation solution agents contain dimethyl sulfoxide (DMSO), which exhibits strong toxicity and can potentially promote cell differentiation. Hence, it is important to explore substitutes for DMSO in cryoprotectant solutions. One such alternative is StemCell Keep (SCK), a DMSO-free solution that has been reported to effectively cryopreserve human induced pluripotent stem cells (hiPS cells). To clarify the effect of cryopreservation agents on cells, DNA microarray analysis is useful, as it can identify a large number of gene expression differences in cryopreserved cells, as well as functional increases in gene groups. In this study, we performed gene expression analysis of SCK-cryopreserved hiPS cells using a DNA microarray gene chip. The hiPS cells vitrified with SCK or DMSO-based vitrification solutions were thawed and cultured on Matrigel under feeder-free conditions, and RNA was extracted for DNA microarray analysis. Genes obtained from DNA microarray data were classified by the keywords of Gene Ontology Biological Process Term, and their relationships were analyzed using DAVID or the GeneMANIA database. SCK-cryopreserved hiPS cells expressed several anti-apoptotic genes, as well as genes related to cell adhesion or proliferation at levels that were nearly equivalent to those of non-frozen hiPS cells. Gene enrichment analysis with selected genes of SCK-cryopreserved hiPS cells whose expression differences were superior to those of DAP-cryopreserved showed strong interactions of negative regulation of apoptotic process, cell adhesion and positive regulation of cell proliferation in DAVID analysis. We demonstrated that SCK successfully maintained the key functions of hiPS cells, including anti-apoptosis, cell adhesion, and cell proliferation, during cryopreservation. Elsevier 2021-11-15 /pmc/articles/PMC8605251/ /pubmed/34825070 http://dx.doi.org/10.1016/j.bbrep.2021.101172 Text en © 2021 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Article
Ota, Akemi
Hyon, Suong-Hyu
Sumi, Shoichiro
Matsumura, Kazuaki
Gene expression analysis of human induced pluripotent stem cells cryopreserved by vitrification using StemCell Keep
title Gene expression analysis of human induced pluripotent stem cells cryopreserved by vitrification using StemCell Keep
title_full Gene expression analysis of human induced pluripotent stem cells cryopreserved by vitrification using StemCell Keep
title_fullStr Gene expression analysis of human induced pluripotent stem cells cryopreserved by vitrification using StemCell Keep
title_full_unstemmed Gene expression analysis of human induced pluripotent stem cells cryopreserved by vitrification using StemCell Keep
title_short Gene expression analysis of human induced pluripotent stem cells cryopreserved by vitrification using StemCell Keep
title_sort gene expression analysis of human induced pluripotent stem cells cryopreserved by vitrification using stemcell keep
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8605251/
https://www.ncbi.nlm.nih.gov/pubmed/34825070
http://dx.doi.org/10.1016/j.bbrep.2021.101172
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