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Effects of donors’ age and passage number on the biological characteristics of menstrual blood-derived stem cells

机译:供体年龄和传代数对经血来源干细胞生物学特性的影响

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摘要

We investigated the effects of donor age and passage number on the biological characteristics of menstrual blood-derived stem cells (MenSCs) by comparing MenSCs derived from donors with three different age ranges and after different passage times. Continuous passage, flat cloning, cell proliferation assays, flow cytometric phenotyping and whole human genome microarray were performed to systematically analyze the relationship between the self-renewal ability of MenSCs as well as their potential to maintain their stem cell characteristics and to resist aging. The results demonstrated that the immunophenotypes and in vitro cultural characteristics of MenSCs did not change significantly with the progression of aging. However, some important signal pathways including MAPK, the insulin signaling pathway, pathways involved in carcinogenesis such as PPAR and P53, and cytokines and their receptors, as well as other pathways associated with immune response and aging, changed to various extents under the conditions of aging after a long time in vitro. The enriched differentially-expressed genes were mainly involved in transcriptional regulation, stress response, cell proliferation, development and apoptosis. The key differentiallyexpressed genes associated with age and passage number were identified for use as biomarkers of cell aging.
机译:我们通过比较来自三个不同年龄范围和不同传代时间的供体的MenSCs,研究了供体的年龄和传代次数对月经血来源干细胞(MenSCs)生物学特性的影响。进行了连续传代,平板克隆,细胞增殖测定,流式细胞仪表型分析和整个人类基因组芯片研究,以系统分析MenSCs的自我更新能力与其维持干细胞特性和抵抗衰老的潜力之间的关系。结果表明,MenSCs的免疫表型和体外培养特性不会随着衰老的进展而显着变化。但是,一些重要的信号途径包括MAPK,胰岛素信号传导途径,与癌变有关的途径,例如PPAR和P53,以及细胞因子及其受体,以及与免疫反应和衰老相关的其他途径,在以下条件下发生了不同程度的变化:体外长时间老化后。富集的差异表达基因主要参与转录调控,应激反应,细胞增殖,发育和凋亡。与年龄和传代次数有关的关键差异表达基因被鉴定为细胞衰老的生物标志物。

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