Zalessky Alexandr, Fedotov Yuriy, Yashkina Elizaveta, Nadtochenko Viktor, Osipov Andreyan N
N.N. Semenov Federal Research Center for Chemical Physics, Russian Academy of Sciences, 119991 Moscow, Russia.
Moscow Institute of Physics and Technology, Dolgoprudny, 141700 Moscow, Russia.
Molecules. 2021 Jul 1;26(13):4027. doi: 10.3390/molecules26134027.
To assess the prospects for using intense femtosecond laser radiation in biomedicine, it is necessary to understand the mechanisms of its action on biological macromolecules, especially on the informational macromolecule-DNA. The aim of this work was to study the immunocytochemical localization of DNA repair protein foci (XRCC1 and γH2AX) induced by tightly focused femtosecond laser radiation in human cancer A549 cells. The results showed that no XRCC1 or γH2AX foci tracks were observed 30 min after cell irradiation with femtosecond pulses of 10 W∙cm peak power density. An increase in the pulse power density to 2 × 10 W∙cm led to the formation of linear tracks consisting both of XRCC1 and γH2AX protein foci localized in the places where the laser beam passed through the cell nuclei. A further increase in the pulse power density to 4 × 10 W∙cm led to the appearance of nuclei with total immunocytochemical staining for XRCC1 and γH2AX on the path of the laser beam. Thus, femtosecond laser radiation can be considered as a tool for local ionization of biological material, and this ionization will lead to similar effects obtained using ionizing radiation.
为了评估在生物医学中使用强飞秒激光辐射的前景,有必要了解其对生物大分子,尤其是对信息大分子——DNA的作用机制。这项工作的目的是研究在人肺癌A549细胞中,由紧聚焦飞秒激光辐射诱导的DNA修复蛋白病灶(XRCC1和γH2AX)的免疫细胞化学定位。结果表明,在用峰值功率密度为10 W∙cm的飞秒脉冲照射细胞30分钟后,未观察到XRCC1或γH2AX病灶轨迹。当脉冲功率密度增加到2×10 W∙cm时,会形成由XRCC1和γH2AX蛋白病灶组成的线性轨迹,这些病灶位于激光束穿过细胞核的位置。当脉冲功率密度进一步增加到4×10 W∙cm时,在激光束路径上会出现对XRCC1和γH2AX进行全免疫细胞化学染色的细胞核。因此,飞秒激光辐射可被视为一种对生物材料进行局部电离的工具,这种电离将导致与使用电离辐射获得的类似效果。