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增殖细胞核抗原(PCNA)和Ki-67抗原的增强型聚合物一步法染色(EPOS):在术中冰冻诊断中的应用

Enhanced polymer one-step staining (EPOS) for proliferating cell nuclear antigen (PCNA) and Ki-67 antigen: application to intra-operative frozen diagnosis.

作者信息

Tsutsumi Y, Serizawa A, Kawai K

机构信息

Department of Pathology, Tokai University School of Medicine, Isehara, Japan.

出版信息

Pathol Int. 1995 Feb;45(2):108-15. doi: 10.1111/j.1440-1827.1995.tb03430.x.

DOI:10.1111/j.1440-1827.1995.tb03430.x
PMID:7742923
Abstract

Enhanced polymer one-step staining (EPOS) is a novel, highly sensitive one-step immunostaining method. This simple and rapid technique was applied to intra-operative frozen diagnosis. The markers of choice were proliferating cell nuclear antigen (PCNA) and Ki-67 antigen. These cell proliferation markers were both identifiable in fresh frozen sections of the human tonsil in approximately 7 min. The suitable staining sequences are as follows. Frozen sections prepared using 3-aminopropyltrimethoxysilane-coated glass slides are immediately fixed, without air drying, for 15 s in a mixture of 50% formalin and 50% methanol for PCNA, and in 10% formalin for Ki-67 antigen. After a brief rinse in phosphate-buffered saline (PBS), sections are incubated with the EPOS antibody for 3 min, followed by PBS rinse for 1 min. The peroxidase activity is visualized in diaminobenzidine-H2O2 solution containing 10 mmol/L imidazole for 2 min. After a light rinse in tap water, the nuclei are briefly counterstained with 5% methyl green. When necessary, endogenous peroxidase blockage in 1% periodic acid solution for 1 min is added before the EPOS antibody incubation. This procedure is applicable to frozen sections of gastric cancers, malignant lymphomas, and brain, liver and peritoneal lesions in which differential diagnosis between benignancy and malignancy was required.

摘要

增强型聚合物一步染色法(EPOS)是一种新型的、高灵敏度的一步免疫染色方法。这种简单快速的技术被应用于术中冰冻诊断。选用的标志物是增殖细胞核抗原(PCNA)和Ki-67抗原。在人扁桃体的新鲜冰冻切片中,这两种细胞增殖标志物在大约7分钟内均可被识别。合适的染色步骤如下。使用3-氨丙基三甲氧基硅烷包被的载玻片制备的冰冻切片立即固定,无需风干,用50%福尔马林和50%甲醇的混合液固定PCNA 15秒,用10%福尔马林固定Ki-67抗原。在磷酸盐缓冲盐水(PBS)中短暂冲洗后,切片与EPOS抗体孵育3分钟,然后用PBS冲洗1分钟。在含有10 mmol/L咪唑的二氨基联苯胺-H2O2溶液中显色2分钟以显示过氧化物酶活性。在自来水中轻轻冲洗后,细胞核用5%甲基绿进行短暂复染。必要时,在EPOS抗体孵育前加入1%高碘酸溶液封闭内源性过氧化物酶1分钟。该程序适用于需要进行良恶性鉴别诊断的胃癌、恶性淋巴瘤以及脑、肝和腹膜病变的冰冻切片。

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