Maruo N, Nakabo T, Kondo M
J Histochem Cytochem. 1986 Oct;34(10):1253-5. doi: 10.1177/34.10.3745905.
A method was developed for measuring the nuclear DNA content in single cells previously identified on a bone marrow smear stained by the Wright-Giemsa method. The smear was first photographed and the location of individual cells, identified by morphology, was recorded on a cell map. The smear was then bleached with 50% acid ethanol and absolute methanol, and re-stained by the Feulgen method in 0.05% pararosaniline Schiff's reagent (pH 2.3) at 7 degrees C for 10 min. Nuclear red fluorescence was observed and the intensity of this fluorescence was proportional to the amount of DNA after prior irradiation of smears with green light for 9 hr. The method is useful for measuring cell DNA content in heterogeneous cell populations when morphological cell identification is required.
开发了一种用于测量先前在经瑞氏-吉姆萨方法染色的骨髓涂片上鉴定出的单个细胞中核DNA含量的方法。首先对涂片进行拍照,并在细胞图谱上记录通过形态学鉴定的单个细胞的位置。然后用50%酸性乙醇和无水甲醇对涂片进行漂白,并用0.05%副品红席夫试剂(pH 2.3)在7℃下进行孚尔根染色10分钟。在涂片预先用绿光照射9小时后,观察到核红色荧光,且该荧光强度与DNA量成正比。当需要进行细胞形态学鉴定时,该方法可用于测量异质细胞群体中的细胞DNA含量。