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首页> 外文期刊>Folia histochemica et cytobiologica >Transcriptional activity of telomerase complex in CD34- stem cells of cord blood in dependence of preparation time.
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Transcriptional activity of telomerase complex in CD34- stem cells of cord blood in dependence of preparation time.

机译:端粒酶复合物在脐血CD34-干细胞中的转录活性取决于制备时间。

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The aim of the study was to determine whether the expression of telomerase subunits encoding genes changes during the process of cord blood preparation. It should establish if the commonly accepted 24 hours time interval in stem cells kriopreservation procedure significantly influences their immortalization and so decreases the "quality" of cord blood stem cells. Investigation includes 69 women. Spontaneous labour was the inclusion condition. The material was collected at birth after clamping of umbilical cord by direct vasopuncture. CD34- cells were extracted from cord blood (MACS, Miltenyi Biotec; Bisley, Surrey, UK). The expression profile of telomerase activators and inhibitors encoding genes was determined using HG_U133A oligonucleotide microarray (Affymetrix). We used a real-time quantitative RT-PCR assay to quantify the telomerase TERT, hTR and TP1 subunits mRNA copy numbers in CD34- cells in 0, 6, 12 and 24 hours after cord blood collection. We observed significant decrease of numbers of copies of TERTA+B mRNA within the successive hours of observation. Significant decrease of numbers of TERTA mRNA copies was confirmed after 24 hours. However, we observed significant increase of numbers of copies of TERTB mRNA after 6 hours of observation. Similar level was maintained during another 6h. The significantly lower number of copies of TERTB mRNA was observed after 24h. We also observed significant increase of number of copies of TERT mRNA after 6 hours. Number of copies of TERT mRNA significantly decreased after another 6h, remaining, however, on a higher then initial one. The significant lower number of copies of TERT mRNA was observed 24h after delivery. The possible explanation of those results is discussed in the paper.
机译:该研究的目的是确定编码脐带血的端粒酶亚基的表达在脐血制备过程中是否发生变化。它应确定干细胞角膜保存程序中公认的24小时时间间隔是否会显着影响其永生化,从而降低脐带血干细胞的“质量”。调查包括69名妇女。包括自发性劳动。通过直接血管穿刺术夹紧脐带后在出生时收集材料。从脐带血(MACS,Miltenyi Biotec; Bisley,Surrey,UK)中提取CD34-细胞。使用HG_U133A寡核苷酸微阵列(Affymetrix)确定端粒酶激活剂和编码基因的抑制剂的表达谱。我们使用实时定量RT-PCR分析法来量化脐带血收集后0、6、12和24小时内CD34-细胞中的端粒酶TERT,hTR和TP1亚基mRNA拷贝数。我们观察到连续几个小时内TERTA + B mRNA的拷贝数显着减少。 24小时后确认TERTA mRNA拷贝数显着减少。但是,我们观察到6个小时后,TERTB mRNA的拷贝数显着增加。在另外6小时内保持了相似的水平。 24小时后观察到TERTB mRNA的拷贝数显着降低。我们还观察到6小时后TERT mRNA的拷贝数显着增加。 TERT mRNA的拷贝数在另外6h后显着下降,但是仍然比最初高。分娩后24小时观察到TERT mRNA的拷贝数明显减少。本文讨论了这些结果的可能解释。

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