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Autonomous trisomic rescue of Down syndrome cells

Down syndrome is the most frequent chromosomal abnormality among live-born infants. All Down syndrome patients have mental retardation and are prone to develop early onset Alzheimer’s disease. However, it has not yet been elucidated whether there is a correlation between the phenotype of Down syndro...

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Autores principales: Inoue, Momoko, Kajiwara, Kazuhiro, Yamaguchi, Ayumi, Kiyono, Tohru, Samura, Osamu, Akutsu, Hidenori, Sago, Haruhiko, Okamoto, Aikou, Umezawa, Akihiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6760570/
https://www.ncbi.nlm.nih.gov/pubmed/30760866
http://dx.doi.org/10.1038/s41374-019-0230-0
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author Inoue, Momoko
Kajiwara, Kazuhiro
Yamaguchi, Ayumi
Kiyono, Tohru
Samura, Osamu
Akutsu, Hidenori
Sago, Haruhiko
Okamoto, Aikou
Umezawa, Akihiro
author_facet Inoue, Momoko
Kajiwara, Kazuhiro
Yamaguchi, Ayumi
Kiyono, Tohru
Samura, Osamu
Akutsu, Hidenori
Sago, Haruhiko
Okamoto, Aikou
Umezawa, Akihiro
author_sort Inoue, Momoko
collection PubMed
description Down syndrome is the most frequent chromosomal abnormality among live-born infants. All Down syndrome patients have mental retardation and are prone to develop early onset Alzheimer’s disease. However, it has not yet been elucidated whether there is a correlation between the phenotype of Down syndrome and the extra chromosome 21. In this study, we continuously cultivated induced pluripotent stem cells (iPSCs) with chromosome 21 trisomy for more than 70 weeks, and serendipitously obtained revertant cells with normal chromosome 21 diploids from the trisomic cells during long-term cultivation. Repeated experiments revealed that this trisomy rescue was not due to mosaicism of chromosome 21 diploid cells and occurred at an extremely high frequency. We herewith report the spontaneous correction from chromosome 21 trisomy to disomy without genetic manipulation, chemical treatment or exposure to irradiation. The revertant diploid cells will possibly serve a reference for drug screening and a raw material of regenerative medicinal products for cell-based therapy.
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spelling pubmed-67605702019-09-26 Autonomous trisomic rescue of Down syndrome cells Inoue, Momoko Kajiwara, Kazuhiro Yamaguchi, Ayumi Kiyono, Tohru Samura, Osamu Akutsu, Hidenori Sago, Haruhiko Okamoto, Aikou Umezawa, Akihiro Lab Invest Article Down syndrome is the most frequent chromosomal abnormality among live-born infants. All Down syndrome patients have mental retardation and are prone to develop early onset Alzheimer’s disease. However, it has not yet been elucidated whether there is a correlation between the phenotype of Down syndrome and the extra chromosome 21. In this study, we continuously cultivated induced pluripotent stem cells (iPSCs) with chromosome 21 trisomy for more than 70 weeks, and serendipitously obtained revertant cells with normal chromosome 21 diploids from the trisomic cells during long-term cultivation. Repeated experiments revealed that this trisomy rescue was not due to mosaicism of chromosome 21 diploid cells and occurred at an extremely high frequency. We herewith report the spontaneous correction from chromosome 21 trisomy to disomy without genetic manipulation, chemical treatment or exposure to irradiation. The revertant diploid cells will possibly serve a reference for drug screening and a raw material of regenerative medicinal products for cell-based therapy. Nature Publishing Group US 2019-02-13 2019 /pmc/articles/PMC6760570/ /pubmed/30760866 http://dx.doi.org/10.1038/s41374-019-0230-0 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
Inoue, Momoko
Kajiwara, Kazuhiro
Yamaguchi, Ayumi
Kiyono, Tohru
Samura, Osamu
Akutsu, Hidenori
Sago, Haruhiko
Okamoto, Aikou
Umezawa, Akihiro
Autonomous trisomic rescue of Down syndrome cells
title Autonomous trisomic rescue of Down syndrome cells
title_full Autonomous trisomic rescue of Down syndrome cells
title_fullStr Autonomous trisomic rescue of Down syndrome cells
title_full_unstemmed Autonomous trisomic rescue of Down syndrome cells
title_short Autonomous trisomic rescue of Down syndrome cells
title_sort autonomous trisomic rescue of down syndrome cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6760570/
https://www.ncbi.nlm.nih.gov/pubmed/30760866
http://dx.doi.org/10.1038/s41374-019-0230-0
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