Tomasi V H, Orrea S C, Raimondi A R, Itoiz M E
Oral Pathology Department, Faculty of Dentistry, University of Buenos Aires, Argentina.
Biotech Histochem. 2003 Oct;78(5):255-9.
We describe here a new method for specific staining of mast cells using ferroin. Different hamster tissues were fixed in 4% formalin and processed for paraffin embedding. Sections were stained with hematoxylin followed by ferroin acidified with 2.5 N sulfuric acid to pH 4.0. Mast cells stained an intense orange color that contrasted markedly with bluish violet nuclei. High contrast was also observed when ferroin colored sections were counterstained with light green instead of hematoxylin. To evaluate the specificity of the stain, hamster cheek pouch sections were stained with toluidine blue, alcian blue-safranin O, and ferroin. Quantitative evaluation of mast cells stained with the three techniques showed no statistical difference. The simplicity and selectivity of this method is sufficient for image analysis of mast cells.
我们在此描述一种使用邻二氮菲对肥大细胞进行特异性染色的新方法。将不同的仓鼠组织固定于4%福尔马林中,然后进行石蜡包埋处理。切片先用苏木精染色,接着用2.5N硫酸酸化至pH 4.0的邻二氮菲染色。肥大细胞染成强烈的橙色,与蓝紫色的细胞核形成明显对比。当用浅绿色而非苏木精对邻二氮菲染色的切片进行复染时,也观察到了高对比度。为评估该染色的特异性,用甲苯胺蓝、阿尔辛蓝-番红O和邻二氮菲对仓鼠颊囊切片进行染色。对用这三种技术染色的肥大细胞进行定量评估,结果显示无统计学差异。该方法的简单性和选择性足以用于肥大细胞的图像分析。