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Jujuboside A inhibits oxidative stress damage and enhances immunomodulatory capacity of human umbilical cord mesenchymal stem cells through up-regulating IDO expression

间充质干细胞 氧化应激 细胞凋亡 流式细胞术 免疫印迹 药理学 外周血单个核细胞 脐带 化学 丙二醛 癌症研究 医学 免疫学 细胞生物学 生物化学 生物 体外 基因
作者
Ji-Cong CHEN,Honghe Xiao,Qiang Zhang,Liang Kong,Tian-Min WANG,Tian Yu,Yu‐Meng Zhao,He LI,Jin‐Ming Tian,Cui Wang,Jingxian Yang
出处
期刊:Chinese Journal of Natural Medicines [Elsevier BV]
卷期号:20 (7): 494-505 被引量:5
标识
DOI:10.1016/s1875-5364(22)60176-6
摘要

Impaired immunomodulatory capacity and oxidative stress are the key factors limiting the effectiveness of mesenchymal stem cell transplantation therapy. The present study was aimed to investigate the effects of jujuboside A (JuA) on the protective effect and immunomodulatory capacity of human umbilical cord mesenchymal stem cells (hUC-MSCs). Hydrogen peroxide was used to establish an oxidative damage model of hUC-MSCs, while PBMCs isolated from rats were used to evaluate the effect of JuA pre-treatment on the immunomodulatory capacity of hUC-MSCs. Furthermore, Hoechst 33258 staining, lactate dehydrogenase test, measurement of malondialdehyde, Western blot, high-performance liquid chromatography; and flow cytometry were performed. Our results indicated that JuA (25 μmol·L-1) promoted the proliferation of hUC-MSCs, but did not affect the differentiating capability of these cells. JuA pre-treatment inhibited apoptosis, prevented oxidative damage, and up-regulated the protein expression of nuclear factor-erythroid factor 2-related factor 2 and heme oxygenase 1 in hUC-MSCs in which oxidative stress was induced with H2O2. In addition, JuA pre-treatment enhanced the inhibitory effect of hUC-MSCs against abnormally activated PBMCs, which was related to stimulation of the expression and activity of indoleamine 2,3-dioxygenase. In conclusion, our results demonstrate that JuA pre-treatment can enhance the survival and immunomodulatory ability through pathways related to oxidative stress, providing a new option for the improvement of hUC-MSCs in the clinical setting.
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