Kawai K, Serizawa A, Hamana T, Tsutsumi Y
Division of Diagnostic Pathology, Tokai University Hospital, Isehara, Japan.
Pathol Int. 1994 Oct-Nov;44(10-11):759-64. doi: 10.1111/j.1440-1827.1994.tb02923.x.
Immunohistochemical demonstration of proliferating cell nuclear antigen (PCNA) and p53 protein is important, particularly for the surgical diagnosis of neoplastic disorders. An effective, simple and reproducible method was established for observing the expression of these intranuclear antigens in routinely processed, formalin-fixed paraffin-embedded sections. Dramatic improvement of the antigenicity was obtained when the deparaffinized sections were heated in a hot water bath at 90 degrees C for 120 min in 0.01 mol/L citrate buffer, pH 6.0, for PCNA and in 0.01 mol/L phosphate-buffered saline, pH 7.2, for p53 protein. These reliable pretreatments are useful for the detailed comparative analysis of the expression of PCNA and p53 protein and fine histologic architecture and for retrospective study using a large number of archival specimens.
增殖细胞核抗原(PCNA)和p53蛋白的免疫组织化学检测非常重要,特别是对于肿瘤性疾病的外科诊断。我们建立了一种有效、简单且可重复的方法,用于观察这些核内抗原在常规处理的福尔马林固定石蜡包埋切片中的表达。当脱蜡切片在90℃的热水浴中,于pH 6.0的0.01 mol/L柠檬酸盐缓冲液中加热120分钟用于PCNA检测,以及在pH 7.2的0.01 mol/L磷酸盐缓冲盐溶液中加热用于p53蛋白检测时,抗原性得到了显著改善。这些可靠的预处理方法对于PCNA和p53蛋白表达以及精细组织学结构的详细比较分析,以及使用大量存档标本进行回顾性研究都很有用。