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TRPV-1-mediated elimination of residual iPS cells in bioengineered cardiac cell sheet tissues
The development of a suitable strategy for eliminating remaining undifferentiated cells is indispensable for the use of human-induced pluripotent stem (iPS) cell-derived cells in regenerative medicine. Here, we show for the first time that TRPV-1 activation through transient culture at 42 °C in comb...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4757885/ https://www.ncbi.nlm.nih.gov/pubmed/26888607 http://dx.doi.org/10.1038/srep21747 |
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author | Matsuura, Katsuhisa Seta, Hiroyoshi Haraguchi, Yuji Alsayegh, Khaled Sekine, Hidekazu Shimizu, Tatsuya Hagiwara, Nobuhisa Yamazaki, Kenji Okano, Teruo |
author_facet | Matsuura, Katsuhisa Seta, Hiroyoshi Haraguchi, Yuji Alsayegh, Khaled Sekine, Hidekazu Shimizu, Tatsuya Hagiwara, Nobuhisa Yamazaki, Kenji Okano, Teruo |
author_sort | Matsuura, Katsuhisa |
collection | PubMed |
description | The development of a suitable strategy for eliminating remaining undifferentiated cells is indispensable for the use of human-induced pluripotent stem (iPS) cell-derived cells in regenerative medicine. Here, we show for the first time that TRPV-1 activation through transient culture at 42 °C in combination with agonists is a simple and useful strategy to eliminate iPS cells from bioengineered cardiac cell sheet tissues. When human iPS cells were cultured at 42 °C, almost all cells disappeared by 48 hours through apoptosis. However, iPS cell-derived cardiomyocytes and fibroblasts maintained transcriptional and protein expression levels, and cardiac cell sheets were fabricated after reducing the temperature. TRPV-1 expression in iPS cells was upregulated at 42 °C, and iPS cell death at 42 °C was TRPV-1-dependent. Furthermore, TRPV-1 activation through thermal or agonist treatment eliminated iPS cells in cardiac tissues for a final concentration of 0.4% iPS cell contamination. These findings suggest that the difference in tolerance to TRPV-1 activation between iPS cells and iPS cell-derived cardiac cells could be exploited to eliminate remaining iPS cells in bioengineered cell sheet tissues, which will further reduce the risk of tumour formation. |
format | Online Article Text |
id | pubmed-4757885 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47578852016-02-26 TRPV-1-mediated elimination of residual iPS cells in bioengineered cardiac cell sheet tissues Matsuura, Katsuhisa Seta, Hiroyoshi Haraguchi, Yuji Alsayegh, Khaled Sekine, Hidekazu Shimizu, Tatsuya Hagiwara, Nobuhisa Yamazaki, Kenji Okano, Teruo Sci Rep Article The development of a suitable strategy for eliminating remaining undifferentiated cells is indispensable for the use of human-induced pluripotent stem (iPS) cell-derived cells in regenerative medicine. Here, we show for the first time that TRPV-1 activation through transient culture at 42 °C in combination with agonists is a simple and useful strategy to eliminate iPS cells from bioengineered cardiac cell sheet tissues. When human iPS cells were cultured at 42 °C, almost all cells disappeared by 48 hours through apoptosis. However, iPS cell-derived cardiomyocytes and fibroblasts maintained transcriptional and protein expression levels, and cardiac cell sheets were fabricated after reducing the temperature. TRPV-1 expression in iPS cells was upregulated at 42 °C, and iPS cell death at 42 °C was TRPV-1-dependent. Furthermore, TRPV-1 activation through thermal or agonist treatment eliminated iPS cells in cardiac tissues for a final concentration of 0.4% iPS cell contamination. These findings suggest that the difference in tolerance to TRPV-1 activation between iPS cells and iPS cell-derived cardiac cells could be exploited to eliminate remaining iPS cells in bioengineered cell sheet tissues, which will further reduce the risk of tumour formation. Nature Publishing Group 2016-02-18 /pmc/articles/PMC4757885/ /pubmed/26888607 http://dx.doi.org/10.1038/srep21747 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Matsuura, Katsuhisa Seta, Hiroyoshi Haraguchi, Yuji Alsayegh, Khaled Sekine, Hidekazu Shimizu, Tatsuya Hagiwara, Nobuhisa Yamazaki, Kenji Okano, Teruo TRPV-1-mediated elimination of residual iPS cells in bioengineered cardiac cell sheet tissues |
title | TRPV-1-mediated elimination of residual iPS cells in bioengineered cardiac cell sheet tissues |
title_full | TRPV-1-mediated elimination of residual iPS cells in bioengineered cardiac cell sheet tissues |
title_fullStr | TRPV-1-mediated elimination of residual iPS cells in bioengineered cardiac cell sheet tissues |
title_full_unstemmed | TRPV-1-mediated elimination of residual iPS cells in bioengineered cardiac cell sheet tissues |
title_short | TRPV-1-mediated elimination of residual iPS cells in bioengineered cardiac cell sheet tissues |
title_sort | trpv-1-mediated elimination of residual ips cells in bioengineered cardiac cell sheet tissues |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4757885/ https://www.ncbi.nlm.nih.gov/pubmed/26888607 http://dx.doi.org/10.1038/srep21747 |
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