Human umbilical cord mesenchymal stem cells regulate glutathione metabolism depending on the ERK-Nrf2-HO-1 signal pathway to repair phosphoramide mustard-induced ovarian cancer cells.

IF 1.7 4区 生物学 Q3 BIOLOGY
Open Life Sciences Pub Date : 2024-11-16 eCollection Date: 2024-01-01 DOI:10.1515/biol-2022-0997
Lu Sun, Xiaodong Fan, Qian Chen, Guoyan Liu
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Abstract

The aim of this study was to study the effects of human umbilical cord mesenchymal stem cells (HUC-MSCs) on glutathione (GSH) metabolism in human ovarian cancer cells induced by phosphoramide mustard (PM). The experiment was divided into five groups, namely, the blank group (ovarian cancer cells), the control group (ovarian cancer cells + HUC-MSCs), the model group (ovarian cancer cells + PM), the treatment group (ovarian cancer cells + PM + HUC-MSCs), and the inhibitor group (ovarian cancer cells + PM + HUC-MSCs + extracellular signal-regulated protein kinase inhibitor PD98059). The apoptosis rate of ovarian cancer cells was detected by flow cytometry. Intracellular levels of oxidized glutathione (GSSG), GSH, γ-glutamyl cysteine synthetase (γ-GCS), and intracellular reactive oxygen species (ROS) were detected by enzyme-linked immunosorbent assay. Protein imprinting and real-time fluorescence quantitative PCR were used to detect extracellular regulated protein kinase (ERK), p-ERK heme oxygenase-1 (HO-1), and nuclear factor E2-related factor 2 (Nrf2) protein levels. First, the apoptosis rate in the model group was increased compared with that of the blank group. The levels of γ-GCS, p-ERK, HO-1, and Nrf-2 decreased, while the levels of malondialdehyde, GSSG, and ROS increased. Second, compared with the model group, the apoptosis rate in the treatment group decreased. GSH, γ-GCS, p-ERK, HO-1, and Nrf2 levels increased. Malondialdehyde, GSSG, and ROS levels decreased. Third, after the administration of ERK inhibitor, the apoptosis rate of cells increased. GSH, p-ERK, and HO-1 levels decreased. GSSG and ROS levels increased (P < 0.05), and γ-GCS level had a downward trend compared with the treatment group. To conclude, HUC-MSCs may regulate the ERK-Nrf2-HO-1 pathway to increase γ-GCS expression and GSH production, reduce ROS level and apoptosis of ovarian cancer cells, and improve antioxidant capacity.

人脐带间充质干细胞依靠ERK-Nrf2-HO-1信号通路调节谷胱甘肽代谢,以修复磷胺芥子气诱导的卵巢癌细胞。
本研究旨在探讨人脐带间充质干细胞(HUC-MSCs)对磷酰胺芥(PM)诱导的人卵巢癌细胞谷胱甘肽(GSH)代谢的影响。实验分为五组,即空白组(卵巢癌细胞)、对照组(卵巢癌细胞+HUC-间充质干细胞)、模型组(卵巢癌细胞+PM)、治疗组(卵巢癌细胞+PM+HUC-间充质干细胞)和抑制剂组(卵巢癌细胞+PM+HUC-间充质干细胞+胞外信号调节蛋白激酶抑制剂PD98059)。卵巢癌细胞的凋亡率由流式细胞术检测。细胞内氧化谷胱甘肽(GSSG)、GSH、γ-谷氨酰半胱氨酸合成酶(γ-GCS)和细胞内活性氧(ROS)的水平通过酶联免疫吸附试验进行检测。蛋白印迹法和实时荧光定量 PCR 被用来检测细胞外调节蛋白激酶(ERK)、p-ERK 血红素加氧酶-1(HO-1)和核因子 E2 相关因子 2(Nrf2)的蛋白水平。首先,与空白组相比,模型组的细胞凋亡率有所增加。γ-GCS、p-ERK、HO-1 和 Nrf-2 水平下降,而丙二醛、GSSG 和 ROS 水平上升。其次,与模型组相比,治疗组的细胞凋亡率降低。GSH、γ-GCS、p-ERK、HO-1 和 Nrf2 水平升高。丙二醛、GSSG 和 ROS 水平下降。第三,服用 ERK 抑制剂后,细胞凋亡率增加。GSH、p-ERK 和 HO-1 水平下降。与治疗组相比,GSSG 和 ROS 水平升高(P < 0.05),γ-GCS 水平呈下降趋势。总之,HUC-间充质干细胞可调节 ERK-Nrf2-HO-1 通路,增加γ-GCS 的表达和 GSH 的产生,降低 ROS 水平和卵巢癌细胞的凋亡,提高抗氧化能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.50
自引率
4.50%
发文量
131
审稿时长
43 weeks
期刊介绍: Open Life Sciences (previously Central European Journal of Biology) is a fast growing peer-reviewed journal, devoted to scholarly research in all areas of life sciences, such as molecular biology, plant science, biotechnology, cell biology, biochemistry, biophysics, microbiology and virology, ecology, differentiation and development, genetics and many others. Open Life Sciences assures top quality of published data through critical peer review and editorial involvement throughout the whole publication process. Thanks to the Open Access model of publishing, it also offers unrestricted access to published articles for all users.
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