Lähdetie J
Department of Medical Genetics, University of Turku, Finland.
Mutat Res. 1988 Feb;203(1):47-53. doi: 10.1016/0165-1161(88)90007-6.
The induction and survival of micronuclei (MN) in rat spermatids was studied by two different methods, the dissection method (DM) and the suspension method (SM). It was observed that MN are induced by cyclophosphamide in the S phase of meiosis, in preleptotene spermatocytes, and in an earlier cell stage, the type B spermatogonia. Both techniques showed that MN survive in spermatids at least 5 days. Advantages of the DM include the use of a DNA-specific fluorochrome for staining of MN, higher MN frequencies observed, and the possibility to gain detailed information of the kinetics of induction of MN. In the SM, slide preparation is simpler than in the DM, and several samples can be prepared simultaneously but the scoring of slides is time consuming. Improvements of the sampling system of the DM are suggested. For evaluation of clastogenic action of chemicals on male germ cells both techniques provide a simple and rapid approach.
采用两种不同方法,即解剖法(DM)和悬浮法(SM),研究了大鼠精子细胞中微核(MN)的诱导和存活情况。观察到环磷酰胺可在减数分裂的S期、前细线期精母细胞以及更早的细胞阶段(B型精原细胞)诱导产生微核。两种技术均显示微核在精子细胞中至少存活5天。解剖法的优点包括使用DNA特异性荧光染料对微核进行染色、观察到的微核频率更高,以及能够获取微核诱导动力学的详细信息。在悬浮法中,载玻片制备比解剖法更简单,并且可以同时制备多个样本,但载玻片评分耗时。建议对解剖法的采样系统进行改进。对于评估化学物质对雄性生殖细胞的致断裂作用,这两种技术都提供了一种简单快速的方法。