Yekeler H, Erel O, Yumbul A Z, Doymaz M Z, Doğan O, Ozercan M R, Iplikçi A
Department of Pathology, Firat University Medical School, Elaziğ, Turkey.
J Pathol. 1995 Apr;175(4):449-52. doi: 10.1002/path.1711750413.
A sensitive staining method for nucleolar organizer regions (NORs) is described, using blue toning of AgNORs. NORs are loops of DNA which are transcribed into ribosomal RNA. NORs can be demonstrated by staining with silver nitrate, since NOR-associated proteins are argyrophilic, producing structures termed AgNORs. Normal blood lymphocytes were stained with both methods. The number and resolution of NORs increased 2-3 times by blue toning (30 mmol/l FeCl3, 11 mmol/l potassium hexacyanoferrate(III), and 33 mmol/l oxalic acid) compared with silver staining. A significant difference in the number of NORs was noticed between silver-stained and blue-toned cells (P < 0.001). The blue toning technique thus appears to be more sensitive in detecting NORs than the AgNOR method and may prove a useful alternative for applications in histopathology.
本文描述了一种用于核仁组织区(NORs)的灵敏染色方法,即对银染核仁组织区(AgNORs)进行蓝色调色。NORs是DNA环,可转录为核糖体RNA。由于与NOR相关的蛋白质具有嗜银性,用硝酸银染色可显示出NORs,从而产生被称为AgNORs的结构。用这两种方法对正常血液淋巴细胞进行染色。与银染相比,通过蓝色调色(30 mmol/l三氯化铁、11 mmol/l铁氰化钾(III)和33 mmol/l草酸),NORs的数量和分辨率提高了2至3倍。在银染细胞和蓝色调色细胞之间观察到NORs数量存在显著差异(P < 0.001)。因此,蓝色调色技术在检测NORs方面似乎比AgNOR方法更灵敏,可能成为组织病理学应用中的一种有用替代方法。