用JSB-1单克隆抗体检测B-5固定和石蜡包埋细胞系和组织中的p -糖蛋白。

Z P Pavelic, Z Sever, R N Fontaine, V V Baker, J Reising, D M Denton, L Pavelic, M Khalily
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引用次数: 15

摘要

我们利用JSB-1单克隆抗体(MAb)免疫组化分析了p -糖蛋白(Pgp)在多药耐药(MDR) (CHrC5和CEM- vlb)和敏感(AuxB1和CEM)细胞系石蜡包埋切片上的表达,以及在正常肾脏、结肠、肾上腺、肾癌和结肠癌中的表达。通过比较三种不同免疫组化技术的敏感性,发现过氧化物酶-抗过氧化物酶法是最好的。然后我们测试了六种不同的固定方法。B-5固定剂对MDR细胞株和人体组织的染色效果最强。两种MDR细胞系,但在1%多聚甲醛和Zamboni固定液中固定的组织均呈弱染色。MDR细胞系和组织在10%的缓冲或非缓冲福尔马林或组织处理的AMeX方法中均未检测到免疫反应性。本研究清楚地表明,固定剂的类型对于保存被JSB-1 MAb识别的Pgp表位至关重要,并且B-5固定剂有望同样适用于正常组织和肿瘤组织中Pgp的检测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Detection of P-glycoprotein with JSB-1 monoclonal antibody in B-5 fixed and paraffin-embedded cell lines and tissues.

We analyzed the expression of P-glycoprotein (Pgp) by immunohistochemistry using JSB-1 monoclonal antibody (MAb) on paraffin-embedded sections of the multi-drug resistant (MDR) (CHrC5 and CEM-VLB), and sensitive (AuxB1 and CEM) cell lines, and also in normal kidney, colon, adrenal and in kidney and colon carcinomas. After comparing the sensitivity of three different immunohistochemical techniques the peroxidase-antiperoxidase method was found to be the best. We then tested six different fixation methods. The MDR cell lines and human tissues demonstrated the strongest staining with B-5 fixative. Both MDR cell lines, but not the tissues fixed in 1% paraformaldehyde and Zamboni's fixative demonstrated weak staining. No immuno- reactivity could be detected in MDR cell lines and tissues fixed in 10% buffered or nonbuffered formalin or by the AMeX method of tissue processing. The present study clearly shows that the type of fixative is critical for the preservation of Pgp epitope recognized by JSB-1 MAb, and that B-5 fixative is expected to be equally applicable for the detection of Pgp in normal and neoplastic tissues.

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