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Selective Elimination of Human Induced Pluripotent Stem Cells Using Medium with High Concentration of L-Alanine

Human pluripotent stem cells, including human induced pluripotent stem cells (hiPSCs), serve as highly valuable sources for both cell-based therapies and basic research, owing to their abilities to self-renew and differentiate into any cell type of the human body. However, tumorigenic risks of resid...

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Autores principales: Nagashima, Takunori, Shimizu, Kazunori, Matsumoto, Ryo, Honda, Hiroyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6102287/
https://www.ncbi.nlm.nih.gov/pubmed/30127448
http://dx.doi.org/10.1038/s41598-018-30936-2
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author Nagashima, Takunori
Shimizu, Kazunori
Matsumoto, Ryo
Honda, Hiroyuki
author_facet Nagashima, Takunori
Shimizu, Kazunori
Matsumoto, Ryo
Honda, Hiroyuki
author_sort Nagashima, Takunori
collection PubMed
description Human pluripotent stem cells, including human induced pluripotent stem cells (hiPSCs), serve as highly valuable sources for both cell-based therapies and basic research, owing to their abilities to self-renew and differentiate into any cell type of the human body. However, tumorigenic risks of residual undifferentiated stem cells limit the clinical application of hiPSCs, necessitating methods to eliminate undifferentiated hiPSCs from differentiated cells. Here, we found that undifferentiated hiPSCs were more sensitive to the treatment with a medium supplemented with high concentration of L-alanine than human fibroblasts (hFBs), human skeletal muscle cells (hSkMCs), hiPSC-derived cardiomyocytes (iCMs) or hiPSC-derived fibroblast-like cells (iFLCs), which were used as differentiated cells. Undifferentiated hiPSCs co-cultured with differentiated cells were selectively eliminated following treatment. In addition, we found that the medium supplemented with high concentration of D-alanine or β-alanine also induced cell death of hiPSCs and the treatment at 4 °C didn’t induce cell death of hiPSCs. The cell death induced would be associated partly with high osmotic pressure of the medium supplemented with L-alanine. As L-alanine is a component of proteins in human body and popular ingredient of cell culture media, treatment with high concentration of L-alanine may be useful for eliminating tumorigenic residual hiPSCs for stem cell-based therapies.
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spelling pubmed-61022872018-08-27 Selective Elimination of Human Induced Pluripotent Stem Cells Using Medium with High Concentration of L-Alanine Nagashima, Takunori Shimizu, Kazunori Matsumoto, Ryo Honda, Hiroyuki Sci Rep Article Human pluripotent stem cells, including human induced pluripotent stem cells (hiPSCs), serve as highly valuable sources for both cell-based therapies and basic research, owing to their abilities to self-renew and differentiate into any cell type of the human body. However, tumorigenic risks of residual undifferentiated stem cells limit the clinical application of hiPSCs, necessitating methods to eliminate undifferentiated hiPSCs from differentiated cells. Here, we found that undifferentiated hiPSCs were more sensitive to the treatment with a medium supplemented with high concentration of L-alanine than human fibroblasts (hFBs), human skeletal muscle cells (hSkMCs), hiPSC-derived cardiomyocytes (iCMs) or hiPSC-derived fibroblast-like cells (iFLCs), which were used as differentiated cells. Undifferentiated hiPSCs co-cultured with differentiated cells were selectively eliminated following treatment. In addition, we found that the medium supplemented with high concentration of D-alanine or β-alanine also induced cell death of hiPSCs and the treatment at 4 °C didn’t induce cell death of hiPSCs. The cell death induced would be associated partly with high osmotic pressure of the medium supplemented with L-alanine. As L-alanine is a component of proteins in human body and popular ingredient of cell culture media, treatment with high concentration of L-alanine may be useful for eliminating tumorigenic residual hiPSCs for stem cell-based therapies. Nature Publishing Group UK 2018-08-20 /pmc/articles/PMC6102287/ /pubmed/30127448 http://dx.doi.org/10.1038/s41598-018-30936-2 Text en © The Author(s) 2018 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
Nagashima, Takunori
Shimizu, Kazunori
Matsumoto, Ryo
Honda, Hiroyuki
Selective Elimination of Human Induced Pluripotent Stem Cells Using Medium with High Concentration of L-Alanine
title Selective Elimination of Human Induced Pluripotent Stem Cells Using Medium with High Concentration of L-Alanine
title_full Selective Elimination of Human Induced Pluripotent Stem Cells Using Medium with High Concentration of L-Alanine
title_fullStr Selective Elimination of Human Induced Pluripotent Stem Cells Using Medium with High Concentration of L-Alanine
title_full_unstemmed Selective Elimination of Human Induced Pluripotent Stem Cells Using Medium with High Concentration of L-Alanine
title_short Selective Elimination of Human Induced Pluripotent Stem Cells Using Medium with High Concentration of L-Alanine
title_sort selective elimination of human induced pluripotent stem cells using medium with high concentration of l-alanine
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6102287/
https://www.ncbi.nlm.nih.gov/pubmed/30127448
http://dx.doi.org/10.1038/s41598-018-30936-2
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