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作 者:黎佼[1] 胡明[1] 李国强[1] 莫沛[1] 刘建卫[1] 曾波航[1] 董珺[1] 刘世明[1]
机构地区:[1]广州医科大学附属第二医院广州心血管疾病研究所,广州510260
出 处:《广东医学》2015年第10期1501-1504,共4页Guangdong Medical Journal
基 金:国家自然科学基金资助项目(编号:81401156);广州市医药卫生科技项目(编号:20141A011085)
摘 要:目的探讨年青人骨髓间充质干细胞(h MSCs)来源生物活性因子对年老人h MSCs功能的影响。方法低氧无血清培养条件下获得年青及年老h MSCs条件培养基(CM)。将年老h MSCs置于年青h MSCs来源CM中,或相反将年青h MSCs置于年老h MSCs来源CM中。通过Transwell实验、油红O染色、茜素红染色、β半乳糖苷酶染色、qRT-PCR分别检测不同来源CM中生物活性因子对h MSCs迁移能力、向脂肪细胞及成骨细胞分化能力、衰老、microRNA表达的影响。结果年青h MSCs来源CM生物活性因子可促进年老h MSCs功能再生,增强迁移能力和向脂肪细胞及成骨细胞分化能力,减少衰老。相反,将年青h MSCs置于年老h MSCs来源CM中,年青h MSCs功能受损,迁移能力下降,向脂肪细胞及成骨细胞分化能力下降,衰老增加。qRT-PCR检测发现,年青h MSCs来源CM生物活性因子可促进h MSCs中miR-10a表达,而年老h MSCs来源CM生物活性因子可抑制其表达。结论年青h MSCs来源生物活性因子可促进miR-10a表达,促进h MSCs迁移、分化,减少细胞衰老,促进年老h MSCs功能再生。Objective To investigate the effects of human mesenchymal stem cells( h MSCs) derived bioactive factors on h MSCs function.Methods Old h MSCs were exposed to a young cell derived condition medium( CM).Conversely,young h MSCs were exposed to an old cell derived CM.The transwell tests were used to detect the migration capability of h MSCs.The differentiation capability was compared by inducing h MSCs into adipogenic and osteogenic cells.The effect of condition medium bioactive factors on h MSCsenescence were detected by β-galactosidase staining.The changes in microRNA( miRNA) expression were determined by quantitative real-time PCR( qRT-PCR).Results Old h MSCs can be rejuvenated by exposure to a young cell derived CM.The h MSCmigration and differentiation ability was increased,and senescence was decreased.Conversely,the migration and differentiation ability of young h MSCs was impaired by exposure to an old cell derived CM.And the senescence was increased.The expression of miR-10 a was down-regulated in the old h MSCs derived CM,but was up-regulated in the young h MSCs derived CM.Conclusion Young cell derived bioactive factors can rejuvenate old h MSC function by increasing the expression of miR-10 a.
分 类 号:R329.2[医药卫生—人体解剖和组织胚胎学]
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