Pavelic Z P, Sever Z, Fontaine R N, Baker V V, Reising J, Denton D M, Pavelic L, Khalily M
Department of Pathology, College of Medicine, University of Cincinnati, Ohio 45267-0529.
Sel Cancer Ther. 1991 Summer;7(2):49-58. doi: 10.1089/sct.1991.7.49.
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.
我们使用JSB - 1单克隆抗体(MAb),通过免疫组织化学方法,在多药耐药(MDR)(CHrC5和CEM - VLB)及敏感(AuxB1和CEM)细胞系的石蜡包埋切片上,以及在正常肾脏、结肠、肾上腺组织和肾癌、结肠癌组织中分析了P - 糖蛋白(Pgp)的表达。在比较了三种不同免疫组织化学技术的敏感性后,发现过氧化物酶 - 抗过氧化物酶方法是最佳的。然后我们测试了六种不同的固定方法。多药耐药细胞系和人体组织经B - 5固定剂处理后染色最强。两种多药耐药细胞系经1%多聚甲醛和赞博尼固定剂处理后染色较弱,而组织经这两种固定剂处理后则无此现象。用10%缓冲或非缓冲福尔马林固定的多药耐药细胞系和组织,或采用AMeX组织处理方法处理的细胞系和组织,均未检测到免疫反应性。本研究清楚地表明,固定剂类型对于保存JSB - 1 MAb识别的Pgp表位至关重要,并且预计B - 5固定剂同样适用于检测正常组织和肿瘤组织中的Pgp。