Biliński S M, Bilińska B
Department of Systematic Zoology, Jagiellonian University, Kraków, Poland.
Histochem J. 1996 Sep;28(9):651-6. doi: 10.1007/BF02331386.
The Ag-NOR staining technique is widely used for visualizing nucleolar organizer regions (NORs) in various plant and animal tissues. We describe a simple and time-saving combination of Ag-NOR staining with DNA detection by fluorescence microscopy. This modification was tested on cultured cells and semi-thin sections of plastic-embedded tissues. Of the different fixatives and embedding media used in our studies, the best results (i.e., high selectivity of staining, and lack of or very low background precipitation) were obtained with fixation in methanol-acetone at-20 degrees C for cultured cells, and fixation in 4% formaldehyde followed by embedding in Histocryl resin for tissue sections. The optimal time of Ag-NOR staining was determined experimentally for all materials tested. The specificity of the staining was checked at the electron microscopical level. Especially good results were obtained by mixing epifluorescence with standard bright-field illumination. In such a combination, Ag-NOR-positive nucleoli, or their fibrillar centres and dense fibrillar components, were clearly visible against a bright background of nuclear DNA.
银染核仁组织区(Ag-NOR)技术被广泛用于观察各种动植物组织中的核仁组织区(NORs)。我们描述了一种将Ag-NOR染色与荧光显微镜DNA检测相结合的简单且省时的方法。这种改进方法在培养细胞和塑料包埋组织的半薄切片上进行了测试。在我们研究中使用的不同固定剂和包埋介质中,对于培养细胞,在-20℃用甲醇-丙酮固定可获得最佳结果(即染色的高选择性以及背景沉淀极少或没有);对于组织切片,先用4%甲醛固定,然后用Histocryl树脂包埋可获得最佳结果。通过实验确定了所有测试材料的Ag-NOR染色最佳时间。在电子显微镜水平检查了染色的特异性。将落射荧光与标准明场照明相结合可获得特别好的结果。在这种组合中,Ag-NOR阳性核仁或其纤维中心和致密纤维成分在核DNA的明亮背景下清晰可见。