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γ射线多剂量照射后处于平台期的C3H 10T1/2细胞中损伤积累和修复能力降低的证据。

Evidence for reduced capacity for damage accumulation and repair in plateau-phase C3H 10T1/2 cells following multiple-dose irradiation with gamma rays.

作者信息

Ngo F Q, Youngman K, Suzuki S, Koumoundouros I, Iliakis G

出版信息

Radiat Res. 1986 Jun;106(3):380-95.

PMID:3714980
Abstract

The effects of multiple-dose gamma irradiation on the shape of survival curves were studied with mouse C3H 10T1/2 cells maintained in contact-inhibited plateau phase. The dose-fractionation intervals included 3, 6, and 24 h. Following three fractionated doses (5 Gy per dose) of exposures, cells responded to further irradiation by displaying a survival curve with a much reduced shoulder width (Dq) compared to that of the survival curve measured in cells irradiated with single-graded doses alone. The effect on the mean lethal dose (D0) was small and appeared to be significant. The effect on reduction of Dq could not be completely overcome by lengthening the fractionation intervals from 3 to 6 h or 24 h, times in which repair of sublethal damage (SLD) measured by simple split-dose scheme and potentially lethal damage (PLD) measured by postirradiation incubation was completed. Other experiments showed that pretreatments of cells with fractionated irradiation appeared to slow down the cellular repair processes of SLD and PLD. Therefore, the observed change in the shape of survival curves after fractionation treatments may be attributed to a reduction of the cells' capacity for damage accumulation by an enhancement of the lethal expression of SLD and PLD. Although the molecular mechanism(s) is not known, the results of this study indicate that the acute graded dose-survival curve cannot be used a priori to extrapolate and reliably predict results of hyperfractionation. It is probable that for a nondividing or slowly dividing cell population, such an extrapolation may lead to an underestimation of cell killing. Furthermore, the findings of this investigation appear to support an interpretation, alternative to the high-linear energy transfer (LET) track-end postulate, for the effects on cell survival seen at low doses or low dose rates.

摘要

利用处于接触抑制平台期的小鼠C3H 10T1/2细胞,研究了多剂量γ射线照射对存活曲线形状的影响。剂量分割间隔包括3小时、6小时和24小时。在进行三次分次照射(每次剂量5 Gy)后,与仅接受单次分级剂量照射的细胞相比,细胞对进一步照射的反应是存活曲线的肩宽(Dq)大幅减小。对平均致死剂量(D0)的影响较小,但似乎具有显著性。将分割间隔从3小时延长至6小时或24小时(通过简单的分次剂量方案测量的亚致死损伤(SLD)修复以及通过照射后孵育测量的潜在致死损伤(PLD)修复完成的时间),并不能完全克服对Dq的减小作用。其他实验表明,用分次照射对细胞进行预处理似乎会减缓SLD和PLD的细胞修复过程。因此,分次处理后存活曲线形状的观察变化可能归因于通过增强SLD和PLD的致死表达而降低了细胞损伤积累的能力。尽管分子机制尚不清楚,但本研究结果表明,急性分级剂量存活曲线不能先验地用于外推并可靠地预测超分割的结果。对于非分裂或缓慢分裂的细胞群体,这样的外推可能会导致对细胞杀伤的低估。此外,本研究结果似乎支持了一种与高线性能量转移(LET)径迹末端假设不同的解释,用于解释低剂量或低剂量率下对细胞存活的影响。

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