Ilyas AbdulMojeed O, Alam Md Kowsar, Musah Jamal-Deen, Yang Mengsu, Lam Yun Wah, Roy Vellaisamy A L, Lau Condon
Department of Physics, City University of Hong Kong, Kowloon 999077, Hong Kong SAR, China.
Department of Physics, Federal University Oye-Ekiti, Oye-Ekiti, Ekiti State 3600001, Nigeria.
ACS Omega. 2021 May 26;6(22):13995-14003. doi: 10.1021/acsomega.0c05888. eCollection 2021 Jun 8.
The impact of radiation-induced bystander effect (RIBE) is still not well understood in radiotherapy. RIBEs are biological effects expressed by nonirradiated cells near or far from the irradiated cells. Most radiological studies on cancer cells have been based on biochemical characterization. However, biophysical investigation with label-free techniques to analyze and compare the direct irradiation effect and RIBE has lagged. In this work, we employed an electrical cell-indium tin oxide (ITO) substrate impedance system (ECIIS) as a bioimpedance sensor to evaluate the HeLa cells' response. The bioimpedance of untreated/nonirradiated HeLa (N-HeLa) cells, α-particle (Am-241)-irradiated HeLa (I-HeLa) cells, and bystander HeLa (B-HeLa) cells exposed to media from I-HeLa cells was monitored with a sampling interval of 8 s over a period of 24 h. Also, we imaged the cells at times where impedance changes were observed. Different radiation doses (0.5 cGy, 1.2 cGy, and 1.7 cGy) were used to investigate I-HeLa and B-HeLa cells' radiation-dose-dependence. By analyzing the changes in absolute impedance and cell size/number with time, compared to N-HeLa cells, B-HeLa cells mimicked the I-HeLa cells' damage and modification of proliferation rate. Contrary to the irradiated cells, the bystander cells' damage rate and proliferation rate enhancements have an inverse radiation-dose-response. Also, we report multiple RIBEs in HeLa cells in a single measurement and provide crucial insights into the RIBE mechanism without any labeling procedure. Unambiguously, our results have shown that the time-dependent control of RIBE is important during α-radiation-based radiotherapy of HeLa cells.
在放射治疗中,辐射诱导的旁观者效应(RIBE)的影响仍未得到充分理解。RIBE是由受照射细胞附近或远处的未受照射细胞所表现出的生物学效应。大多数关于癌细胞的放射学研究都基于生化特征。然而,采用无标记技术来分析和比较直接照射效应和RIBE的生物物理研究却滞后了。在这项工作中,我们采用了一种基于细胞 - 铟锡氧化物(ITO)基底的阻抗系统(ECIIS)作为生物阻抗传感器来评估HeLa细胞的反应。以8秒的采样间隔,在24小时内监测未处理/未受照射的HeLa(N - HeLa)细胞、α粒子(Am - 241)照射的HeLa(I - HeLa)细胞以及暴露于I - HeLa细胞培养基中的旁观者HeLa(B - HeLa)细胞的生物阻抗。此外,我们在观察到阻抗变化的时间点对细胞进行成像。使用不同的辐射剂量(0.5 cGy、1.2 cGy和1.7 cGy)来研究I - HeLa和B - HeLa细胞的辐射剂量依赖性。通过分析绝对阻抗和细胞大小/数量随时间的变化,与N - HeLa细胞相比,B - HeLa细胞模拟了I - HeLa细胞的损伤和增殖速率的改变。与受照射细胞相反,旁观者细胞的损伤率和增殖速率增强呈现出相反的辐射剂量反应。此外,我们在单次测量中报告了HeLa细胞中的多种RIBE,并在无需任何标记程序的情况下对RIBE机制提供了关键见解。毫无疑问,我们的结果表明,在基于α辐射的HeLa细胞放射治疗过程中,对RIBE进行时间依赖性控制非常重要。