Shi S R, Chaiwun B, Young L, Cote R J, Taylor C R
Department of Pathology, University of Southern California School of Medicine, Los Angeles 90033.
J Histochem Cytochem. 1993 Nov;41(11):1599-604. doi: 10.1177/41.11.7691930.
We developed a staining protocol for demonstration of androgen receptor (AR) in formalin-fixed, paraffin-embedded tissue sections. The method is based on the antigen retrieval microwave (MW) heating technique. Results are compared with different types of enzyme digestion pre-treatments. The strongest immunostaining signal and clearest background were obtained by MW heating of dewaxed paraffin sections in 5% urea or citrate buffer solution (pH 6); pure distilled water gave less consistent results. Enzymatic digestion with pepsin (0.05% in 2 N HCl) for 30 min at room temperature, or trypsin followed by pronase, or pronase digestion alone, also produced enhanced staining of AR in some cases, but there was more nonspecific background, and specific reactivity was less intense. The antigen retrieval MW method can be used to demonstrate AR epitope in prostate tissue after fixation in formalin for as long as 7 days. AR immunolocalization was also compared in frozen and paraffin sections processed from the same specimen of prostate carcinoma tissue and was found to be qualitatively and quantitatively similar. This study also provided new information concerning the basic principles of the antigen retrieval MW method that may be helpful in further development of this technique.
我们开发了一种用于在福尔马林固定、石蜡包埋的组织切片中显示雄激素受体(AR)的染色方案。该方法基于抗原修复微波(MW)加热技术。将结果与不同类型的酶消化预处理进行比较。通过在5%尿素或柠檬酸盐缓冲溶液(pH 6)中对脱蜡的石蜡切片进行MW加热,可获得最强的免疫染色信号和最清晰的背景;单纯蒸馏水得到的结果不太一致。在室温下用胃蛋白酶(2N HCl中0.05%)消化30分钟,或先用胰蛋白酶再用链霉蛋白酶,或仅用链霉蛋白酶消化,在某些情况下也能增强AR的染色,但非特异性背景更多,特异性反应性较弱。抗原修复MW方法可用于显示在福尔马林固定长达7天的前列腺组织中的AR表位。还对来自同一前列腺癌组织标本的冷冻切片和石蜡切片中的AR免疫定位进行了比较,发现其在定性和定量上相似。本研究还提供了有关抗原修复MW方法基本原理的新信息,这可能有助于该技术的进一步发展。