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Monitoring Glutathione Dynamics and Heterogeneity in Living Stem Cells
Glutathione (GSH) is a major antioxidant in cells, and plays vital roles in the cellular defense against oxidants and in the regulation of redox signals. In a previous report, we demonstrated that stem cell function is critically affected by heterogeneity and dynamic changes in cellular GSH concentr...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Society for Stem Cell Research
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6657947/ https://www.ncbi.nlm.nih.gov/pubmed/30836726 http://dx.doi.org/10.15283/ijsc18151 |
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author | Jeong, Eui Man Shin, Ji-Woong Lim, Jisun Kim, Ju Hwan Kang, Hyewon Yin, Yingfu Kim, Hye-Mi Kim, YongHwan Kim, Sun-Gi Kang, Heun-Soo Shin, Dong-Myung Choi, Kihang Kim, In-Gyu |
author_facet | Jeong, Eui Man Shin, Ji-Woong Lim, Jisun Kim, Ju Hwan Kang, Hyewon Yin, Yingfu Kim, Hye-Mi Kim, YongHwan Kim, Sun-Gi Kang, Heun-Soo Shin, Dong-Myung Choi, Kihang Kim, In-Gyu |
author_sort | Jeong, Eui Man |
collection | PubMed |
description | Glutathione (GSH) is a major antioxidant in cells, and plays vital roles in the cellular defense against oxidants and in the regulation of redox signals. In a previous report, we demonstrated that stem cell function is critically affected by heterogeneity and dynamic changes in cellular GSH concentration. Here, we present a detailed protocol for the monitoring of GSH concentration in living stem cells using FreSHtracer, a real-time GSH probe. We describe the steps involved in monitoring GSH concentration in single living stem cells using confocal microscopy and flow cytometry. These methods are simple, rapid, and quantitative, and able to demonstrate intracellular GSH concentration changes in real time. We also describe the application of FreSHtracer to the sorting of stem cells according to their GSH content using flow cytometry. Typically, microscopic or flow cytometric analyses of FreSHtracer and MitoFreSHtracer signals in living stem cells take ~2~3 h, and the fractionation of stem cells into subpopulations on the basis of cellular GSH levels takes 3~4.5 h. This method could be applied to almost every kind of mammalian cell with minor modifications to the protocol described here. |
format | Online Article Text |
id | pubmed-6657947 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Korean Society for Stem Cell Research |
record_format | MEDLINE/PubMed |
spelling | pubmed-66579472019-07-29 Monitoring Glutathione Dynamics and Heterogeneity in Living Stem Cells Jeong, Eui Man Shin, Ji-Woong Lim, Jisun Kim, Ju Hwan Kang, Hyewon Yin, Yingfu Kim, Hye-Mi Kim, YongHwan Kim, Sun-Gi Kang, Heun-Soo Shin, Dong-Myung Choi, Kihang Kim, In-Gyu Int J Stem Cells Technical Report Glutathione (GSH) is a major antioxidant in cells, and plays vital roles in the cellular defense against oxidants and in the regulation of redox signals. In a previous report, we demonstrated that stem cell function is critically affected by heterogeneity and dynamic changes in cellular GSH concentration. Here, we present a detailed protocol for the monitoring of GSH concentration in living stem cells using FreSHtracer, a real-time GSH probe. We describe the steps involved in monitoring GSH concentration in single living stem cells using confocal microscopy and flow cytometry. These methods are simple, rapid, and quantitative, and able to demonstrate intracellular GSH concentration changes in real time. We also describe the application of FreSHtracer to the sorting of stem cells according to their GSH content using flow cytometry. Typically, microscopic or flow cytometric analyses of FreSHtracer and MitoFreSHtracer signals in living stem cells take ~2~3 h, and the fractionation of stem cells into subpopulations on the basis of cellular GSH levels takes 3~4.5 h. This method could be applied to almost every kind of mammalian cell with minor modifications to the protocol described here. Korean Society for Stem Cell Research 2019-02-28 /pmc/articles/PMC6657947/ /pubmed/30836726 http://dx.doi.org/10.15283/ijsc18151 Text en Copyright © 2019 by the Korean Society for Stem Cell Research This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Technical Report Jeong, Eui Man Shin, Ji-Woong Lim, Jisun Kim, Ju Hwan Kang, Hyewon Yin, Yingfu Kim, Hye-Mi Kim, YongHwan Kim, Sun-Gi Kang, Heun-Soo Shin, Dong-Myung Choi, Kihang Kim, In-Gyu Monitoring Glutathione Dynamics and Heterogeneity in Living Stem Cells |
title | Monitoring Glutathione Dynamics and Heterogeneity in Living Stem Cells |
title_full | Monitoring Glutathione Dynamics and Heterogeneity in Living Stem Cells |
title_fullStr | Monitoring Glutathione Dynamics and Heterogeneity in Living Stem Cells |
title_full_unstemmed | Monitoring Glutathione Dynamics and Heterogeneity in Living Stem Cells |
title_short | Monitoring Glutathione Dynamics and Heterogeneity in Living Stem Cells |
title_sort | monitoring glutathione dynamics and heterogeneity in living stem cells |
topic | Technical Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6657947/ https://www.ncbi.nlm.nih.gov/pubmed/30836726 http://dx.doi.org/10.15283/ijsc18151 |
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