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低剂量辐射对人淋巴细胞微核的诱导作用。

The induction of micronuclei in human lymphocytes by low doses of radiation.

作者信息

Mitchell J C, Norman A

机构信息

Department of Radiological Sciences, UCLA School of Medicine 90024.

出版信息

Int J Radiat Biol Relat Stud Phys Chem Med. 1987 Oct;52(4):527-35. doi: 10.1080/09553008714552031.

Abstract

The appearance of micronuclei (MN) is delayed with respect to cell division in populations of irradiated human lymphocytes, so that the length of time in culture, as well as the number of divisions, is a factor in MN assays. Using two assays that control for cell kinetics, we measured the yield of cells with MN exposed to graded doses of 60Co gamma rays and 90KVP X-rays. The yields showed a non-linear increase with dose. They can be represented by two straight lines: the one in the range below 0.15 Gy has a slight slope, the other in the range above 0.15 Gy has a significantly greater slope. The radical scavengers cysteamine and glycerol, which reduced the MN yields sharply at 3 Gy, were less effective at 0.3 Gy, indicating that terminal deletions arising from the direct ionization of DNA are a major source of the MN induced by low radiation doses. It is likely that the non-linear dose response is due to the saturation of a DNA repair process.

摘要

在受辐照的人类淋巴细胞群体中,微核(MN)的出现相对于细胞分裂有所延迟,因此培养时间以及分裂次数都是微核检测中的影响因素。我们使用两种控制细胞动力学的检测方法,测量了暴露于不同剂量60Coγ射线和90KVP X射线的含有微核的细胞产量。产量随剂量呈非线性增加。它们可以由两条直线表示:一条在低于0.15 Gy的范围内斜率较小,另一条在高于0.15 Gy的范围内斜率显著更大。自由基清除剂半胱胺和甘油在3 Gy时能大幅降低微核产量,但在0.3 Gy时效果较差,这表明DNA直接电离产生的末端缺失是低辐射剂量诱导微核的主要来源。非线性剂量反应可能是由于DNA修复过程的饱和所致。

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