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The impact of long-term in vitro expansion on the senescence-associated markers of human adipose-derived stem cells

机译:长期体外扩增对人脂肪干细胞衰老相关标志物的影响

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摘要

Human adipose-derived stem cells (ASCs) have generated a great deal of excitement in regenerative medicine. However, their safety and efficacy issue remain a major concern especially after long-term in vitro expansion. The aim of this study was to investigate the fundamental changes of ASCs in long-term culture by studying the morphological feature, growth kinetic, surface marker expressions, expression level of the senescenceassociated genes, cell cycle distribution and ?-galactosidase activity. Human ASCs were harvested from lipoaspirate obtained from 6 patients. All the parameters mentioned above were measured at P5, P10, P15 and P20. Data were subjected to one-way analysis of variance with a Tukey post hoc test to determine significance difference (P<0.05). The data showed that growth of ASCs reduced in long-term culture and the ?-galactosidase activity was significantly increased at later passage (P20). The morphology of ASCs in long-term culture showed the manifestation of senescent feature at P15 and P20. Significant alteration in the senescence-associated genes expression levels was observed in MMP1, p21, Rb and Cyclin D1 at P15 and P20. Significant increase in CD45 and HLA DR DQ DP surface marker was observed at P20. While cell cycle analysis showed significant decrease in percentage of ASCs at S and G2/M phase at later passage (P15). Our data showed ASCs cultured beyond P10 favours the senescence pathway and its clinical usage in cell-based therapy may be limited.
机译:人类脂肪干细胞(ASC)在再生医学中引起了极大的兴奋。但是,它们的安全性和功效问题仍然是主要关注的问题,尤其是在长期体外扩增后。这项研究的目的是通过研究形态特征,生长动力学,表面标志物表达,衰老相关基因的表达水平,细胞周期分布和β-半乳糖苷酶活性,来研究长期培养的ASCs的基本变化。从6位患者获得的脂肪抽吸物中收获人ASC。上述所有参数均在P5,P10,P15和P20处测量。使用Tukey post hoc检验对数据进行单向方差分析,以确定显着性差异(P <0.05)。数据表明,长期培养后ASCs的生长减少,β-半乳糖苷酶活性在以后的传代中显着增加(P20)。长期培养的ASCs的形态在P15和P20处表现出衰老特征。在P15和P20的MMP1,p21,Rb和Cyclin D1中观察到衰老相关基因表达水平的显着变化。在P20处观察到CD45和HLA DR DQ DP表面标志物显着增加。细胞周期分析显示,在以后的传代中,S和G2 / M期的ASC百分比显着下降(P15)。我们的数据显示,培养超过P10的ASC有利于衰老途径,其在基于细胞的治疗中的临床应用可能受到限制。

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