Satra Maria, Tsougos Ioannis, Papanikolaou Vassilios, Theodorou Kyriaki, Kappas Constantine, Tsezou Aspasia
Department of Biology, University of Thessaly, Medical School, Larissa, Greece.
Int J Radiat Biol. 2006 Jun;82(6):401-9. doi: 10.1080/09553000600800090.
To quantify and correlate human telomerase reverse transcriptase (hTERT) mRNA expression with telomerase activity (TA) after ionizing irradiation of HeLa cells.
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.
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.
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.
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。
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。
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。
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。