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Autoclave Antigen Retrieval Technique for Immunohistochemical Staining of Androgen Receptor in Formalin-Fixed Paraffin Sections of Human Prostate

机译:高压灭菌抗原修复技术用于人前列腺福尔马林固定石蜡切片中雄激素受体的免疫组织化学染色

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摘要

Although information on the states of androgen receptor (AR) expression at the individual cell level is essential in understanding the human diseased prostate, histological approaches are often hampered by the artifactual loss of AR or AR antigenicity. Here we examined the effects of various antigen retrieval methods, including microwave irradiation and autoclave treatment, for immunohistochemical detection of AR in cultured LNCaP cells and paraffin embedded sections of human prostate, and found beneficial effects of autoclave treatment over microwave treatment. Staining results were consistent with that of AR messenger RNA expression assessed by the reverse transcriptase-polymerase chain reaction method. The procedures described in this article provided intense and reproducible immunostaining for AR, estrogen receptor and progesterone receptor in paraffin sections of the human diseased prostate. Finally, 0.01M EDTA (pH7.4) gave us the most intense nuclear signal for the steroid hormone receptors, though the best soaking solution was 0.01M citrate buffer (pH6.0) considering the lost of tissue morphology.
机译:尽管有关单个细胞水平上雄激素受体(AR)表达状态的信息对于了解人类患病的前列腺至关重要,但组织学方法通常因人为丧失AR或AR抗原性而受到阻碍。在这里,我们检查了各种抗原回收方法的影响,包括微波照射和高压灭菌处理,用于免疫组化检测培养的LNCaP细胞和人前列腺石蜡包埋的切片中的AR,发现高压灭菌处理优于微波处理。染色结果与通过逆转录酶-聚合酶链反应法评估的AR信使RNA表达一致。本文所述的程序为人类患病前列腺的石蜡切片中的AR,雌激素受体和孕酮受体提供了强烈且可重复的免疫染色。最后,考虑到组织形态的损失,尽管最佳的浸泡溶液是0.01M柠檬酸盐缓冲液(pH6.0),但0.01M EDTA(pH7.4)给了我们最强烈的甾类激素受体核信号。

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