Evaluation of Kohlrabi (Brassica oleracea Var. Gongylodes) Extract Effect on Mesenchymal Stem Cells Viability and Apoptosis

Naser Kalhor Qom, Mohsen Sheykhhasan, A. Kowsari
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引用次数: 2

Abstract

BackgroundCell viability and apoptosis are two crucial factors that may determine cell fate. There are several factors, such as hypoxia, which may be effective in cell processes. Because of its unique features, such as its antioxidant, anti-inflammatory, and anti-apoptosis mechanisms, kohlrabi (Brassica oleracea var. gongylodes) extract may be used in the amelioration of cell viability and a decrease in cell apoptosis. In this study, we evaluate the effect of kohlrabi extract on the viability and apoptosis of adipose-derived mesenchymal stem cells (AD-MSCs).Material and MethodsIn this study, extract from kohlrabi and mesenchymal stem cells from adipose tissue were isolated in a laboratory under sterile conditions. Expression of mesenchymal stem cell (MSC) surface markers, including CD44, CD90, and CD105 was evaluated by flow cytometry method. Besides, CD34 was used as a negative marker. MTT assay was carried out to determine the cell viability. Evaluation of BCL2 and BAX expression levels was performed by real-time PCR.ResultsMSC surface markers were verified by flow cytometry. The obtained results demonstrated a significant difference between the cell viability of the kohlrabi-extract treated and control group over time (P=0.03). In addition, the real-time PCR analysis showed that expression levels of BCL2 significantly increased in hypoxic condition after treatment with leaf extract (P=0.019). However, there was no significant expression change in the BAX gene.ConclusionOur study illustrates that kohlrabi extract may have positive effects on cell survival while having inhibitory effects on apoptosis.
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甘蓝提取物对间充质干细胞活力和凋亡的影响
细胞活力和凋亡是决定细胞命运的两个关键因素。有几个因素,如缺氧,可能在细胞过程中有效。由于其独特的抗氧化、抗炎和抗细胞凋亡的作用机制,大头菜提取物可用于改善细胞活力和减少细胞凋亡。在这项研究中,我们评估了大头菜提取物对脂肪源性间充质干细胞(AD-MSCs)活力和凋亡的影响。材料与方法本研究在实验室无菌条件下分离大头菜提取物和脂肪组织间充质干细胞。流式细胞术检测间充质干细胞(MSC)表面标志物CD44、CD90和CD105的表达。CD34作为阴性标记物。采用MTT法测定细胞活力。实时荧光定量PCR检测BCL2和BAX的表达水平。结果smsc表面标记物经流式细胞术验证。结果表明,处理过的大头菜提取物与对照组的细胞活力随时间的变化有显著差异(P=0.03)。此外,实时荧光定量PCR分析显示,叶片提取物处理后,低氧条件下BCL2表达水平显著升高(P=0.019)。而BAX基因的表达无明显变化。结论大头菜提取物对细胞存活有积极作用,对细胞凋亡有抑制作用。
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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