Ex-vivo dose response characterization of the recently identified EDA2R gene after low level radiation exposures and comparison with FDXR gene expression and the γH2AX focus assay.

IF 2.1 4区 医学 Q2 BIOLOGY
Simone Schüle, Carsten Hackenbroch, Meinrad Beer, Razan Muhtadi, Cornelius Hermann, Samantha Stewart, Daniel Schwanke, Patrick Ostheim, Matthias Port, Harry Scherthan, Michael Abend
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引用次数: 1

Abstract

Objective: Recently, promising radiation-induced EDA2R gene expression (GE) changes after low level radiation could be shown. Stimulated by that, in this study, we intended to independently validate these findings and to further characterize dose-response relationships in comparison to FDXR and the γH2AX-DNA double-strand break (DSB) focus assay, since both assays are already widely used for biodosimetry purposes.

Materials and methods: Peripheral blood samples from six healthy human donors were irradiated ex vivo (dose: ranging from 2.6 to 49.7 mGy). Subsequently, the fold-differences relative to the sham irradiated reference group were calculated. Radiation-induced changes in GE of FDXR and EDA2R were examined using the quantitative real-time polymerase-chain-reaction (qRT-PCR). DSB foci were quantified in 100 γH2AX + 53BP1 immunostained cells employing fluorescence microscopy. Examinations were performed at single time points enabling sufficient detection of both endpoints.

Results: A significant increase in EDA2R GE relative to the unexposed control was observed in the range of 2.6 mGy (1.6-fold, p = .045) to 5.4 mGy (2.2-fold, p = .0002), whereas the copy numbers increased linearly up to 13.1-fold at 49.7 mGy. On the contrary, FDXR upregulation (2.2-fold) became significant after a 22.6 mGy exposure (p ≤ .02) and increased linearly up to 4-fold at 49.7 mGy. A significant increase in radiation-induced foci (relative to unexposed, RIF-fd) was observed after 11.3 mGy (RIF-fd: 1.5 ± 0.5, p ≤ .03), while the foci increased linearly up to 3-fold at 49.7 mGy. From this, the FDXR and RIF-fd slopes have shown comparability, while the EDA2R slope was five times higher. Nevertheless, the coefficient of variation (CV) of EDA2R was about 30% higher than for RIF-fd.

Conclusion: Higher radiation-induced EDA2R GE changes and a lower radiation detection level compared to RIF-fd and FDXR GE changes examined under optimal conditions ex vivo on human samples appear promising. Yet, our results represent just the beginning of further studies to be conducted in animal models for further time- and dose-dependent evaluation and additional examinations on radiologically examined patients to evaluate the impact of confounder, such as age, sex, social behavior, or diseases.

最近鉴定的EDA2R基因在低水平辐射暴露后的离体剂量反应特征,并与FDXR基因表达和γH2AX焦点分析进行比较。
目的:近年来,低水平辐射后辐射诱导的EDA2R基因表达(GE)变化有望得到证实。受此刺激,在本研究中,我们打算独立验证这些发现,并与FDXR和γH2AX-DNA双链断裂(DSB)焦点分析相比,进一步表征剂量-反应关系,因为这两种分析都已广泛用于生物剂量测定目的。材料和方法:对来自6名健康人供体的外周血样本进行离体照射(剂量:2.6至49.7mGy)。随后,计算相对于假照射参考组的倍数差异。用定量实时聚合酶链反应(qRT-PCR)检测辐射诱导的FDXR和EDA2R的GE变化。使用荧光显微镜在100γH2AX+53BP1免疫染色的细胞中定量DSB病灶。在单个时间点进行检查,从而能够充分检测两个终点。结果:在2.6 mGy(1.6倍,p = .045)至5.4 mGy(2.2倍,p = .0002),而拷贝数在49.7mGy时线性增加至13.1倍。相反,在22.6mGy暴露后,FDXR上调(2.2倍)变得显著(p ≤ .02),并在49.7mGy时线性增加至4倍。11.3 mGy后,观察到辐射诱导的病灶(相对于未暴露的RIF-fd)显著增加(RIF-fd:1.5 ± 0.5,p ≤ .03),而病灶在49.7mGy时线性增加至3倍。由此,FDXR和RIF fd斜率显示出可比性,而EDA2R斜率高出五倍。然而,EDA2R的变异系数(CV)比RIF-fd高出约30%。结论:与在最佳条件下对人体样本进行体外检测的RIF-fd和FDXR-GE变化相比,更高的辐射诱导EDA2R-GE变化和更低的辐射检测水平似乎是有希望的。然而,我们的结果只是在动物模型中进行进一步研究的开始,以进行进一步的时间和剂量依赖性评估,并对放射学检查的患者进行额外的检查,以评估混杂因素的影响,如年龄、性别、社会行为或疾病。
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来源期刊
CiteScore
5.00
自引率
11.50%
发文量
142
审稿时长
3 months
期刊介绍: The International Journal of Radiation Biology publishes original papers, reviews, current topic articles, technical notes/reports, and meeting reports on the effects of ionizing, UV and visible radiation, accelerated particles, electromagnetic fields, ultrasound, heat and related modalities. The focus is on the biological effects of such radiations: from radiation chemistry to the spectrum of responses of living organisms and underlying mechanisms, including genetic abnormalities, repair phenomena, cell death, dose modifying agents and tissue responses. Application of basic studies to medical uses of radiation extends the coverage to practical problems such as physical and chemical adjuvants which improve the effectiveness of radiation in cancer therapy. Assessment of the hazards of low doses of radiation is also considered.
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