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HeLa细胞中辐射诱导的端粒酶活性与人端粒酶逆转录酶mRNA表达之间的相关性。

Correlation between radiation-induced telomerase activity and human telomerase reverse transcriptase mRNA expression in HeLa cells.

作者信息

Satra Maria, Tsougos Ioannis, Papanikolaou Vassilios, Theodorou Kyriaki, Kappas Constantine, Tsezou Aspasia

机构信息

Department of Biology, University of Thessaly, Medical School, Larissa, Greece.

出版信息

Int J Radiat Biol. 2006 Jun;82(6):401-9. doi: 10.1080/09553000600800090.

Abstract

PURPOSE

To quantify and correlate human telomerase reverse transcriptase (hTERT) mRNA expression with telomerase activity (TA) after ionizing irradiation of HeLa cells.

MATERIALS AND METHODS

TA and hTERT mRNA expression were evaluated, at 24-h intervals, in HeLa cells cultured for up to 144 h, before and after treatment with increasing doses of 6 MV photon ionizing radiation (5 - 20 Gy), using the telomeric repeat amplification protocol (TRAP) assay and real-time reverse transcriptase polymerase chain reaction (RT-PCR), respectively. Cell viability was determined using the 3-(4,5-dimethylthiazole-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) assay. A prototype phantom was constructed for accurate irradiation of HeLa cells.

RESULTS

Treated cells showed a decrease in viability with increasing radiation dose, and a correlation was observed with post-treatment period. TA and hTERT mRNA expression of HeLa cells increased for the first 24 h after irradiation. The maximal increases were approximately two times the un-irradiated cell levels at 24 h post-irradiation, followed by a decrease and a return to the control levels 72 h post-irradiation. The time-course of telomerase activation after 24 h, differed among radiation doses. A dose-dependent G2/M arrest was observed 24 h post-irradiation, along with an increase in polyploidy 48 h post-irradiation and afterwards.

CONCLUSION

A correlation between TA and hTERT mRNA expression and a radiation induced cell cycle dependent modification of hTERT mRNA expression was established for the first 24 h post-irradiation.

摘要

目的

对HeLa细胞进行电离辐射后,定量分析人端粒酶逆转录酶(hTERT)mRNA表达,并将其与端粒酶活性(TA)进行关联分析。

材料与方法

使用端粒重复序列扩增法(TRAP)和实时逆转录聚合酶链反应(RT-PCR),分别在接受递增剂量(5 - 20 Gy)的6 MV光子电离辐射处理前后,以24小时为间隔,对培养长达144小时的HeLa细胞中的TA和hTERT mRNA表达进行评估。使用3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)法测定细胞活力。构建了一个用于精确照射HeLa细胞的原型体模。

结果

随着辐射剂量增加,处理后的细胞活力下降,且与处理后的时间段存在相关性。HeLa细胞的TA和hTERT mRNA表达在辐射后的最初24小时内增加。最大增幅约为辐射后24小时未照射细胞水平的两倍,随后下降,并在辐射后72小时恢复到对照水平。辐射24小时后端粒酶激活的时间进程在不同辐射剂量之间存在差异。辐射后24小时观察到剂量依赖性的G2/M期阻滞,辐射后48小时及之后多倍体增加。

结论

在辐射后最初24小时内,建立了TA与hTERT mRNA表达之间的相关性以及辐射诱导的hTERT mRNA表达的细胞周期依赖性修饰。

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