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Quantifying Biophoton Emissions From Human Cells Directly Exposed toLow-Dose Gamma Radiation

机译:量化直接暴露于人体细胞的生物光子排放低剂量伽玛射线

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摘要

Biophoton emission leading to bystander effects (BEs) was shown inbeta-irradiated cells; however, technical challenges precluded the analysis ofthe biophoton role in gamma-induced BEs. The present work was to design anexperimental approach to determine if, what type, and how many biophotons couldbe produced in gamma-irradiated cells. Photon emission was measured in HCT116p53 cells irradiated with a total dose of 22 mGy from acesium-137 source at a dose rate of 45 mGy/min. A single-photon detection unitwas used and shielded with lead to reduce counts from stray gammas reaching thedetector. Higher quantities of photon emissions were observed when the cells ina tissue culture vessel were present and being irradiated compared to acell-free vessel. Photon emissions were captured at either 340 nm (in theultraviolet A [UVA] range) or 610 nm. At the same cell density, radiationexposure time, and radiation dose, HCT116 p53 cells emitted 2.5times more UVA biophotons than 610-nm biophotons. For the first time, gammaradiation was shown to induce biophoton emissions from biological cells. Ascellular emissions of UVA biophotons following beta radiation lead to BEs, theinvolvement of cellular emissions of the same type of UVA biophotons in gammaradiation-induced BEs is highly likely.
机译:图中显示了导致旁观者效应(BEs)的生物光子发射。β射线照射的细胞;但是,技术挑战使分析生物光子在γ诱导的BE中的作用。目前的工作是设计一个确定是否,什么类型以及有多少生物光子的实验方法在伽马射线照射的细胞中产生。在HCT116中测量了光子发射从p53细胞照射的总剂量为22 mGy的p53细胞。铯137源的剂量率为45 mGy / min。单光子检测单元被使用并用铅屏蔽以减少由于杂散伽马到达探测器。当细胞进入时,观察到更高数量的光子发射。与之相比,存在组织培养容器并受到照射无细胞血管。在340 nm处捕获光子发射(在紫外线A [UVA]范围)或610 nm。在相同的细胞密度下,辐射暴露时间和辐射剂量,HCT116 p53细胞发射2.5是610纳米生物光子的两倍。第一次,伽玛辐射被证明可诱导生物细胞释放生物光子。如β辐射后,UVA生物光子的细胞发射导致BEs,γ中相同类型的UVA生物光子的细胞发射参与辐射诱发的BEs非常可能。

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