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Calcium-independent disruption of microtubule dynamics by nanosecond pulsed electric fields in U87 human glioblastoma cells

机译:U87人胶质母细胞瘤细胞中纳秒脉冲电场的微管动态的钙无关中断

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High powered, nanosecond duration, pulsed electric fields (nsPEF) cause cell death by a mechanism that is not fully understood and have been proposed as a targeted cancer therapy. Numerous chemotherapeutics work by disrupting microtubules. As microtubules are affected by electrical fields, this study looks at the possibility of disrupting them electrically with nsPEF. Human glioblastoma cells (U87-MG) treated with 100, 10?ns, 44?kV/cm pulses at a frequency of 10?Hz showed a breakdown of their interphase microtubule network that was accompanied by a reduction in the number of growing microtubules. This effect is temporally linked to loss of mitochondrial membrane potential and independent of cellular swelling and calcium influx, two factors that disrupt microtubule growth dynamics. Super-resolution microscopy revealed microtubule buckling and breaking as a result of nsPEF application, suggesting that nsPEF may act directly on microtubules.
机译:高功率,纳秒持续时间,脉冲电场(NSPEF)引起细胞死亡通过不完全理解的机制引起细胞死亡,并且已被提出作为靶向癌症治疗。通过破坏微管,众多化学治疗方法。由于微管受电场影响,这项研究看起来有可能用nspef电动破坏它们。用100,10Ω·ns,44Ω·kV / cm脉冲处理的人胶质母细胞瘤细胞(U87-mg)显示出10≤Hz的频率,显示它们的间间微管网络的分解,其伴随着减少生长微管的数量。这种效果在时间上与线粒体膜电位的丧失和无关的细胞溶胀和钙流入,两个因素破坏了微管生长动态。超分辨率显微镜显示MicroTubule屈曲和由于NPPEF应用而破碎,表明NSPEF可以直接作用于微管。

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