Farahzadi Raheleh, Fathi Ezzatollah, Mesbah-Namin Seyed Alireza, Zarghami Nosratollah
Hematology and Oncology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Department of Clinical Biochemistry, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.
PLoS One. 2017 Nov 16;12(11):e0188052. doi: 10.1371/journal.pone.0188052. eCollection 2017.
The use of mesenchymal stem cells (MSCs) for cell therapy and regenerative medicine has received widespread attention over the past few years, but their application can be complicated by factors such as reduction in proliferation potential, the senescent tendency of the MSCs upon expansion and their age-dependent decline in number and function. It was shown that all the mentioned features were accompanied by a reduction in telomerase activity and telomere shortening. Furthermore, the role of epigenetic changes in aging, especially changes in promoter methylation, was reported. In this study, MSCs were isolated from the adipose tissue with enzymatic digestion. In addition, immunocytochemistry staining and flow cytometric analysis were performed to investigate the cell-surface markers. In addition, alizarin red-S, sudan III, toluidine blue, and cresyl violet staining were performed to evaluate the multi-lineage differentiation of hADSCs. In order to improve the effective application of MSCs, these cells were treated with 1.5 × 10-8 and 2.99 × 10-10 M of ZnSO4 for 48 hours. The length of the absolute telomere, human telomerase reverse transcriptase (hTERT) gene expression, telomerase activity, the investigation of methylation status of the hTERT gene promoter and the percentage of senescent cells were analyzed with quantitative real-time PCR, PCR-ELISA TRAP assay, methylation specific PCR (MSP), and beta-galactosidase (SA-β-gal) staining, respectively. The results showed that the telomere length, the hTERT gene expression, and the telomerase activity had significantly increased. In addition, the percentage of senescent cells had significantly decreased and changes in the methylation status of the CpG islands in the hTERT promoter region under treatment with ZnSO4 were seen. In conclusion, it seems that ZnSO4 as a proper antioxidant could improve the aging-related features due to lengthening of the telomeres, increasing the telomerase gene expression, telomerase activity, decreasing aging, and changing the methylation status of hTERT promoter; it could potentially beneficial for enhancing the application of aged-MSCs.
在过去几年中,间充质干细胞(MSCs)用于细胞治疗和再生医学已受到广泛关注,但其应用可能因多种因素而变得复杂,如增殖潜能降低、MSCs在扩增时的衰老倾向以及其数量和功能随年龄的下降。研究表明,上述所有特征均伴随着端粒酶活性降低和端粒缩短。此外,还报道了表观遗传变化在衰老中的作用,尤其是启动子甲基化的变化。在本研究中,通过酶消化从脂肪组织中分离出MSCs。此外,进行了免疫细胞化学染色和流式细胞术分析以研究细胞表面标志物。另外,进行茜素红-S、苏丹III、甲苯胺蓝和甲酚紫染色以评估人脂肪来源干细胞(hADSCs)的多向分化。为了改善MSCs的有效应用,用1.5×10-8和2.99×10-10 M的硫酸锌(ZnSO4)处理这些细胞48小时。分别用定量实时PCR、PCR-ELISA TRAP检测、甲基化特异性PCR(MSP)和β-半乳糖苷酶(SA-β-gal)染色分析绝对端粒长度、人端粒酶逆转录酶(hTERT)基因表达、端粒酶活性、hTERT基因启动子甲基化状态以及衰老细胞百分比。结果表明,端粒长度、hTERT基因表达和端粒酶活性显著增加。此外,衰老细胞百分比显著降低,并且在用ZnSO4处理下hTERT启动子区域的CpG岛甲基化状态发生了变化。总之,似乎ZnSO4作为一种合适的抗氧化剂可以通过延长端粒、增加端粒酶基因表达、端粒酶活性、减少衰老以及改变hTERT启动子的甲基化状态来改善与衰老相关的特征;它可能对增强衰老MSCs的应用有益。