Streffer C, Müller W U, Kryscio A, Böcker W
Institut für Medizinische Strahlenbiologie, Universitätsklinikum Essen, D-45122 Essen, Germany.
Mutat Res. 1998 Aug 3;404(1-2):101-5. doi: 10.1016/s0027-5107(98)00100-6.
Micronuclei can be measured through a conventional method after staining with Giemsa or fluorescence dyes for DNA. However, a technique with cell proliferation control should be preferred. This is done by incubation with cytochalasin B and counting the micronuclei in binucleated cells. Satisfactory dose relationships are observed after irradiation of human lymphocytes in vitro. The RBE for fast neutrons is around three. An automatic analysis is possible by image analysis. The dose range in which significant increases can be observed is 0.3 to 5 Gy X-rays. The assay becomes more sensitive when the micronuclei are determined only in B-lymphocytes. Another possibility exists by determination of the number of micronuclei with centromeres. For this purpose the hybridization with pancentromeric DNA probes and fluorescence labelling is of advantage. By this technique a radiation dose of 0.1 Gy X-rays can be detected. It is apparently also possible under these conditions to detect radiation exposures which have taken place decades before the measurements.
微核可以在使用吉姆萨染料或用于DNA的荧光染料染色后,通过传统方法进行测量。然而,应优先选择具有细胞增殖控制的技术。这可以通过用细胞松弛素B孵育并对双核细胞中的微核进行计数来实现。体外照射人淋巴细胞后可观察到令人满意的剂量关系。快中子的相对生物效应约为3。通过图像分析可以进行自动分析。可观察到显著增加的剂量范围是0.3至5 Gy X射线。当仅在B淋巴细胞中测定微核时,该检测方法会变得更加灵敏。通过确定具有着丝粒的微核数量还有另一种可能性。为此,与全着丝粒DNA探针杂交并进行荧光标记是有优势的。通过这种技术,可以检测到0.1 Gy X射线的辐射剂量。显然,在这些条件下也有可能检测到在测量前几十年发生的辐射暴露。