Hough Cameron M, Purschke David N, Bell Clayton, Kalra Aarat P, Oliva Patricia J, Huang Chenxi, Tuszynski Jack A, Warkentin Brad J, Hegmann Frank A
Department of Oncology, University of Alberta, Edmonton, AB T6G 2E1, Canada.
Department of Physics, University of Alberta, Edmonton, AB T6G 2E1, Canada.
Biomed Opt Express. 2021 Aug 24;12(9):5812-5828. doi: 10.1364/BOE.433240. eCollection 2021 Sep 1.
The biological effects of terahertz (THz) radiation have been observed across multiple levels of biological organization, however the sub-cellular mechanisms underlying the phenotypic changes remain to be elucidated. Filamentous protein complexes such as microtubules are essential cytoskeletal structures that regulate diverse biological functions, and these may be an important target for THz interactions underlying THz-induced effects observed at the cellular or tissue level. Here, we show disassembly of microtubules within minutes of exposure to extended trains of intense, picosecond-duration THz pulses. Further, the rate of disassembly depends on THz intensity and spectral content. As inhibition of microtubule dynamics is a mechanism of clinically-utilized anti-cancer agents, disruption of microtubule networks may indicate a potential therapeutic mechanism of intense THz pulses.
太赫兹(THz)辐射的生物学效应已在多个生物组织层面被观察到,然而,表型变化背后的亚细胞机制仍有待阐明。丝状蛋白复合物,如微管,是调节多种生物学功能的重要细胞骨架结构,这些可能是太赫兹相互作用的重要靶点,其作用机制与在细胞或组织水平观察到的太赫兹诱导效应相关。在此,我们展示了在暴露于持续时间为皮秒的高强度太赫兹脉冲长序列几分钟内微管的解聚。此外,解聚速率取决于太赫兹强度和光谱内容。由于抑制微管动力学是临床使用的抗癌药物的一种作用机制,微管网络的破坏可能表明高强度太赫兹脉冲具有潜在的治疗机制。