Crompton N E, Ozsahin M
Institute for Medical Radiobiology, University of Zurich, Switzerland.
Radiat Res. 1997 Jan;147(1):55-60.
We describe a rapid assay to predict intrinsic radiosensitivity of normal tissues based on the radiation-induced cytotoxic response of a number of types of white blood cells. Twenty-four hours after irradiation, leukocytes were prepared for analysis by flow cytometry. Radiation-induced cytotoxicity was characterized by degradation of internucleosomal DNA, which results in a reduced G1/G0-phase DNA peak. Clear differences in the radiosensitivity of five of six different types of leukocytes were observed. Significant increases in cytotoxicity were observed even at 0.5 Gy, indicating the technique may be useful as a biological dosimeter after radiation accidents. Based on data from 12 healthy blood donors, significant inter-donor differences in radiosensitivity were observed after exposure to 2 or 8 Gy of high-dose-rate X rays. Inter-donor variation was significantly greater than intra-donor variation for both CD4 and CD8 T lymphocytes (P < 0.01), and the technique yielded adequate data to stratify donors based on the radiosensitivities of these two cell types alone, requiring less than 1 ml of blood. The assay is a general assay of early cytotoxic response to radiation-induced damage and should be useful when assaying the response to chemotherapy as well.
我们描述了一种基于多种类型白细胞的辐射诱导细胞毒性反应来预测正常组织内在放射敏感性的快速检测方法。照射后24小时,通过流式细胞术制备白细胞用于分析。辐射诱导的细胞毒性以核小体间DNA降解为特征,这导致G1/G0期DNA峰减少。观察到六种不同类型白细胞中的五种在放射敏感性上存在明显差异。即使在0.5 Gy时也观察到细胞毒性显著增加,表明该技术在辐射事故后作为生物剂量计可能有用。基于12名健康献血者的数据,在暴露于2或8 Gy高剂量率X射线后,观察到供体间在放射敏感性上存在显著差异。对于CD4和CD8 T淋巴细胞,供体间变异显著大于供体内变异(P < 0.01),并且该技术仅基于这两种细胞类型的放射敏感性就能产生足够的数据来对供体进行分层,所需血液量少于1毫升。该检测方法是对辐射诱导损伤的早期细胞毒性反应的通用检测方法,在检测对化疗的反应时也应有用。