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监测活干细胞中的谷胱甘肽动态变化和异质性。

Monitoring Glutathione Dynamics and Heterogeneity in Living Stem Cells.

作者信息

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

机构信息

Department of Biochemistry and Molecular Biology, Seoul National University College of Medicine, Seoul, Korea.

BK21 Plus Biomedical Science Project, Seoul National University, Seoul, Korea.

出版信息

Int J Stem Cells. 2019 Jul 31;12(2):367-379. doi: 10.15283/ijsc18151.

Abstract

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 23 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.

摘要

谷胱甘肽(GSH)是细胞中的主要抗氧化剂,在细胞对抗氧化剂的防御以及氧化还原信号的调节中发挥着至关重要的作用。在之前的一份报告中,我们证明干细胞功能受到细胞内GSH浓度的异质性和动态变化的严重影响。在此,我们介绍一种使用实时GSH探针FreSHtracer监测活干细胞中GSH浓度的详细方案。我们描述了使用共聚焦显微镜和流式细胞术监测单个活干细胞中GSH浓度所涉及的步骤。这些方法简单、快速且定量,能够实时显示细胞内GSH浓度的变化。我们还描述了使用FreSHtracer通过流式细胞术根据干细胞的GSH含量对其进行分选的应用。通常,对活干细胞中FreSHtracer和MitoFreSHtracer信号进行显微镜或流式细胞术分析需要约2至3小时,而根据细胞GSH水平将干细胞分离成亚群需要3至4.5小时。该方法经过对此处所述方案的微小修改后几乎可应用于每一种哺乳动物细胞。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12ca/6657947/a3a6cc0d6545/ijsc-12-367f1.jpg

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