Bundeswehr Institute of Radiobiology Affiliated to University Ulm, Neuherbergstr. 11, 80937, Munich, Germany.
Center for Radiological Research, Columbia University Irving Medical Center (CUIMC), New York, USA.
Sci Rep. 2021 May 7;11(1):9756. doi: 10.1038/s41598-021-88403-4.
Large-scale radiation emergency scenarios involving protracted low dose rate radiation exposure (e.g. a hidden radioactive source in a train) necessitate the development of high throughput methods for providing rapid individual dose estimates. During the RENEB (Running the European Network of Biodosimetry) 2019 exercise, four EDTA-blood samples were exposed to an Iridium-192 source (1.36 TBq, Tech-Ops 880 Sentinal) at varying distances and geometries. This resulted in protracted doses ranging between 0.2 and 2.4 Gy using dose rates of 1.5-40 mGy/min and exposure times of 1 or 2.5 h. Blood samples were exposed in thermo bottles that maintained temperatures between 39 and 27.7 °C. After exposure, EDTA-blood samples were transferred into PAXGene tubes to preserve RNA. RNA was isolated in one laboratory and aliquots of four blinded RNA were sent to another five teams for dose estimation based on gene expression changes. Using an X-ray machine, samples for two calibration curves (first: constant dose rate of 8.3 mGy/min and 0.5-8 h varying exposure times; second: varying dose rates of 0.5-8.3 mGy/min and 4 h exposure time) were generated for distribution. Assays were run in each laboratory according to locally established protocols using either a microarray platform (one team) or quantitative real-time PCR (qRT-PCR, five teams). The qRT-PCR measurements were highly reproducible with coefficient of variation below 15% in ≥ 75% of measurements resulting in reported dose estimates ranging between 0 and 0.5 Gy in all samples and in all laboratories. Up to twofold reductions in RNA copy numbers per degree Celsius relative to 37 °C were observed. However, when irradiating independent samples equivalent to the blinded samples but increasing the combined exposure and incubation time to 4 h at 37 °C, expected gene expression changes corresponding to the absorbed doses were observed. Clearly, time and an optimal temperature of 37 °C must be allowed for the biological response to manifest as gene expression changes prior to running the gene expression assay. In conclusion, dose reconstructions based on gene expression measurements are highly reproducible across different techniques, protocols and laboratories. Even a radiation dose of 0.25 Gy protracted over 4 h (1 mGy/min) can be identified. These results demonstrate the importance of the incubation conditions and time span between radiation exposure and measurements of gene expression changes when using this method in a field exercise or real emergency situation.
在涉及长时间低剂量率辐射暴露的大规模辐射紧急情况(例如火车内隐藏的放射性源)下,需要开发高通量方法来提供快速的个体剂量估算。在 2019 年 RENEB(运行欧洲生物剂量网络)演习中,四个 EDTA 血液样本在不同的距离和几何形状下暴露于铱-192 源(1.36 TBq,Tech-Ops 880 哨兵)。这导致在 1.5-40 mGy/min 的剂量率和 1 或 2.5 小时的暴露时间下,剂量在 0.2 至 2.4 Gy 之间延长。血液样本在保温瓶中暴露,保温瓶维持在 39 至 27.7°C 之间的温度。暴露后,将 EDTA 血液样本转移到 PAXGene 管中以保存 RNA。在一个实验室中分离 RNA,并将四份盲样 RNA 的等分试样发送给另外五个团队,以根据基因表达变化进行剂量估算。使用 X 射线机生成用于两个校准曲线的样本(第一:恒定剂量率为 8.3 mGy/min,暴露时间从 0.5 至 8 小时不等;第二:剂量率从 0.5 至 8.3 mGy/min,暴露时间为 4 小时)进行分布。根据当地建立的协议,在每个实验室中运行化验,使用微阵列平台(一个团队)或定量实时 PCR(qRT-PCR,五个团队)。qRT-PCR 测量结果具有高度可重复性,在 75%以上的测量中,变异系数低于 15%,导致所有样本和所有实验室中的报告剂量估计值在 0 至 0.5 Gy 之间。与 37°C 相比,每摄氏度的 RNA 拷贝数减少了约两倍。然而,当照射与盲样等效的独立样本但将总暴露和孵育时间增加到 37°C 下的 4 小时时,观察到与吸收剂量相对应的预期基因表达变化。显然,在运行基因表达分析之前,必须为生物反应留出时间和最佳温度 37°C,以表现为基因表达变化。总之,基于基因表达测量的剂量重建在不同技术、协议和实验室中具有高度可重复性。即使是延长 4 小时(1 mGy/min)的 0.25 Gy 辐射剂量也可以识别。这些结果表明,在现场演习或实际紧急情况下使用该方法时,在进行基因表达测量之前,孵育条件和辐射暴露与基因表达变化测量之间的时间跨度对该方法非常重要。