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Differentiation potential of Pluripotent Stem Cells correlates to the level of CHD7
Embryonic Stem Cells (ESC) possesses two distinct features; self-renewal and the potential to differentiate. Here we show the differentiation potential and growth rate of ESC correlates positively with the expression level of the gene encoding chromodomain helicase DNA binding protein 7 (CHD7). When...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5762636/ https://www.ncbi.nlm.nih.gov/pubmed/29321579 http://dx.doi.org/10.1038/s41598-017-18439-y |
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author | Yamamoto, Takako Takenaka, Chiemi Yoda, Yusuke Oshima, Yasuhiro Kagawa, Kenichi Miyajima, Hiroshi Sasaki, Tetsuji Kawamata, Shin |
author_facet | Yamamoto, Takako Takenaka, Chiemi Yoda, Yusuke Oshima, Yasuhiro Kagawa, Kenichi Miyajima, Hiroshi Sasaki, Tetsuji Kawamata, Shin |
author_sort | Yamamoto, Takako |
collection | PubMed |
description | Embryonic Stem Cells (ESC) possesses two distinct features; self-renewal and the potential to differentiate. Here we show the differentiation potential and growth rate of ESC correlates positively with the expression level of the gene encoding chromodomain helicase DNA binding protein 7 (CHD7). When ESCs are maintained in feeder-free conditions and single cell seeding, ESC KhES-1 having 4520 copies or more of CHD7 in 5 ng total RNA show differentiation potential, but this is lost when the CHD7 copy number is reduced in KhES-1 to less than 696 by alternative culture conditions. Introduction of siCHD7 reduced differentiation potential and growth rate of KhES-1. Interestingly, KhES-1 underwent spontaneous differentiation when mCHD7 was introduced and we could not obtain CHD7-overexpressing ESC in culture. These data suggest that CHD7 drives differentiation, and there is a lower limit for CHD7 to initiate differentiation and an upper limit for CHD7 if maintained in undifferentiated state, and such upper limit varies depending on culture condition. As CHD7 drives cell growth, ESC with the highest permissible CHD7 level in the given culture become dominant in a couple of passages. Thus, we can select differentiation resistance-free cell clones by optimizing the culture system using CHD7 as an index. |
format | Online Article Text |
id | pubmed-5762636 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57626362018-01-17 Differentiation potential of Pluripotent Stem Cells correlates to the level of CHD7 Yamamoto, Takako Takenaka, Chiemi Yoda, Yusuke Oshima, Yasuhiro Kagawa, Kenichi Miyajima, Hiroshi Sasaki, Tetsuji Kawamata, Shin Sci Rep Article Embryonic Stem Cells (ESC) possesses two distinct features; self-renewal and the potential to differentiate. Here we show the differentiation potential and growth rate of ESC correlates positively with the expression level of the gene encoding chromodomain helicase DNA binding protein 7 (CHD7). When ESCs are maintained in feeder-free conditions and single cell seeding, ESC KhES-1 having 4520 copies or more of CHD7 in 5 ng total RNA show differentiation potential, but this is lost when the CHD7 copy number is reduced in KhES-1 to less than 696 by alternative culture conditions. Introduction of siCHD7 reduced differentiation potential and growth rate of KhES-1. Interestingly, KhES-1 underwent spontaneous differentiation when mCHD7 was introduced and we could not obtain CHD7-overexpressing ESC in culture. These data suggest that CHD7 drives differentiation, and there is a lower limit for CHD7 to initiate differentiation and an upper limit for CHD7 if maintained in undifferentiated state, and such upper limit varies depending on culture condition. As CHD7 drives cell growth, ESC with the highest permissible CHD7 level in the given culture become dominant in a couple of passages. Thus, we can select differentiation resistance-free cell clones by optimizing the culture system using CHD7 as an index. Nature Publishing Group UK 2018-01-10 /pmc/articles/PMC5762636/ /pubmed/29321579 http://dx.doi.org/10.1038/s41598-017-18439-y Text en © The Author(s) 2017 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 Yamamoto, Takako Takenaka, Chiemi Yoda, Yusuke Oshima, Yasuhiro Kagawa, Kenichi Miyajima, Hiroshi Sasaki, Tetsuji Kawamata, Shin Differentiation potential of Pluripotent Stem Cells correlates to the level of CHD7 |
title | Differentiation potential of Pluripotent Stem Cells correlates to the level of CHD7 |
title_full | Differentiation potential of Pluripotent Stem Cells correlates to the level of CHD7 |
title_fullStr | Differentiation potential of Pluripotent Stem Cells correlates to the level of CHD7 |
title_full_unstemmed | Differentiation potential of Pluripotent Stem Cells correlates to the level of CHD7 |
title_short | Differentiation potential of Pluripotent Stem Cells correlates to the level of CHD7 |
title_sort | differentiation potential of pluripotent stem cells correlates to the level of chd7 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5762636/ https://www.ncbi.nlm.nih.gov/pubmed/29321579 http://dx.doi.org/10.1038/s41598-017-18439-y |
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