图案电磁场和发光二极管对癌细胞的影响:单独与同时应用时对细胞密度和生物光子发射的影响

Rahul Ravindran, Kate S. Branigan, Landon M. Lefebvre, Blake T. Dotta
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摘要

以前有报道称,时变电磁场和led具有调节细胞活性和细胞活力的潜力。研究还表明,通过测量来自这些相同细胞的生物光子发射,可以推断细胞的活动和状态。为了确定LED (635 nm, 3 klx)或EMF (1-3 uT)的短暂应用(15分钟)是否会影响细胞生长和随后的生物光子发射特性,将B16-BL6细胞培养至融合,并暴露于时变、调频的EMF、LED或两者中。在EMF和LED暴露前后,以50 Hz的采样率进行1分钟的光子发射测量。在暴露和光子发射测量之后,通过使用血细胞计评估细胞活力。结果表明,与假对照组相比,暴露于时变EMF仅15分钟后,活细胞减少41.6% [t(25) = 2.4, p = 0.02]。这种效应在单独使用LED的情况下接近显著[p = 0.07],但在LED和EMF同时使用的情况下完全不存在[p <0.8]。此外,仅暴露于LED后,全细胞培养物在13 Hz时的生物光子发射SPD值显著增加[t(60) = 2.3, p = 0.021]。该生物光子发射频率也与培养皿中无活细胞的数量密切相关[r =−0.514]。综上所述,这些数据表明,在13赫兹的频率下,细胞培养物发出的生物光子可以作为体外无活细胞数量的潜在指标。这里的数据总结证实了先前的工作,证明了特定时变电磁场作为抑制癌细胞生长的新疗法的有效性。这也进一步证实了我们的观点,即生物光子发射可以作为一种新的细胞活性检测工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of Patterned Electromagnetic Fields and Light-Emitting Diodes on Cancer Cells: Impact on Cell Density and Biophoton Emission When Applied Individually vs. Simultaneously
It has been previously reported that time-varying EMFs and LEDs have the potential to modulate cellular activity and cell viability. It has also been shown that cellular activity and state can be inferred by measuring the biophoton emission derived from these same cells. To identify if the brief application (15 min) of an LED (635 nm at 3 klx) or EMF (1–3 uT) could influence cell growth and subsequent biophoton emission characteristics, B16-BL6 cells were grown to confluence and exposed to a time-varying, frequency-modulated EMF, LED, or both. Before and after EMF and LED exposure, photon emission measurements were taken for 1 min at a 50 Hz sampling rate. Following the exposure and photon emission measurements, cell viability was assessed via the use of a hemocytometer. The results demonstrated that after only 15 min of exposure to a time-varying EMF, there was a 41.6% reduction in viable cells when compared to sham controls [t(25) = 2.4, p = 0.02]. This effect approached significance in the LED alone condition [p = 0.07] but was completely absent in the condition wherein the LED and EMF were applied simultaneously [p < 0.8]. Additionally, following exposure to only the LED, there was a significant increase in biophoton emission SPD values at 13 Hz from whole cell cultures [t(60) = 2.3, p = 0.021]. This biophoton emission frequency was also strongly correlated with the number of nonviable cells [r = −0.514] in the dish. Taken together, these data point to biophotons emitted from cell cultures at 13 Hz as a potential indicator of the number of nonviable cells in vitro. The summation of data here corroborates previous work demonstrating the efficacy of specific time-varying EMFs as a novel therapeutic for the inhibition of cancer cell growth. It also furthers our assertion that biophoton emission can be used as a novel detection tool for cell activity.
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