Muggiolu Giovanna, Torfeh Eva, Simon Marina, Devès Guillaume, Seznec Hervé, Barberet Philippe
University Bordeaux, CNRS, LP2I, UMR 5797, 33170 Gradignan, France.
Biology (Basel). 2023 Jun 27;12(7):921. doi: 10.3390/biology12070921.
Time-lapse fluorescence imaging coupled to micro-irradiation devices provides information on the kinetics of DNA repair protein accumulation, from a few seconds to several minutes after irradiation. Charged-particle microbeams are valuable tools for such studies since they provide a way to selectively irradiate micrometric areas within a cell nucleus, control the dose and the micro-dosimetric quantities by means of advanced detection systems and Monte Carlo simulations and monitor the early cell response by means of beamline microscopy. We used the charged-particle microbeam installed at the AIFIRA facility to perform micro-irradiation experiments and measure the recruitment kinetics of two proteins involved in DNA signaling and repair pathways following exposure to protons and α-particles. We developed and validated image acquisition and processing methods to enable a systematic study of the recruitment kinetics of GFP-XRCC1 and GFP-RNF8. We show that XRCC1 is recruited to DNA damage sites a few seconds after irradiation as a function of the total deposited energy and quite independently of the particle LET. RNF8 is recruited to DNA damage sites a few minutes after irradiation and its recruitment kinetics depends on the particle LET.
延时荧光成像与微辐照装置相结合,可提供有关DNA修复蛋白积累动力学的信息,该信息是关于辐照后几秒到几分钟内的情况。带电粒子微束是此类研究的宝贵工具,因为它们提供了一种选择性辐照细胞核内微米级区域的方法,通过先进的检测系统和蒙特卡罗模拟来控制剂量和微剂量学量,并通过束线显微镜监测细胞的早期反应。我们使用安装在AIFIRA设施的带电粒子微束进行微辐照实验,并测量暴露于质子和α粒子后参与DNA信号传导和修复途径的两种蛋白质的募集动力学。我们开发并验证了图像采集和处理方法,以便能够系统地研究GFP-XRCC1和GFP-RNF8的募集动力学。我们表明,辐照后几秒,XRCC1作为总沉积能量的函数被募集到DNA损伤位点,且相当独立于粒子线性能量转移(LET)。RNF8在辐照后几分钟被募集到DNA损伤位点,其募集动力学取决于粒子LET。