Orchard G E, Calonje E
Department of Dermatopathology, St. John's Dermatology Centre, St. Thomas' Hospital, London, U.K.
Am J Dermatopathol. 1998 Aug;20(4):357-61. doi: 10.1097/00000372-199808000-00006.
The accumulation of excessive amounts of melanin in melanocytic lesions can obscure cellular morphology and can further hinder immunocytochemical procedures. We have used a modification of the potassium permanganate/oxalic acid melanin-bleaching technique, involving much reduced bleaching times, in order to remove melanin granules prior to incubation with primary antibody. We have assessed a panel of antibodies applicable to the evaluation of melanocytic lesions and in addition have also assessed antibodies that may be more useful in research. The study attempts to determine which antigens may be affected by bleaching and which are not. Antigens S100, HMB 45, NKIC3, CD34, and L26 are relatively unaffected by this procedure. Factor-VIII-related antigen and vimentin and CD68 antigens produced enhanced staining. In contrast, antigens CD3, CD31, and CD45RO were abolished. In addition, smooth muscle actin and desmin antigens demonstrated considerable nonspecific background staining and were not reliable in this study. This technique demonstrates that a fairly wide range of antigens are preserved after bleaching and that distinction between melanocytes and melanophages can reliably be performed using the conventional immunocytochemical chromogen 3,3-diaminobenzidine and without the need for elaborate counterstaining.
黑素细胞性病变中过量黑色素的积累会掩盖细胞形态,并进一步阻碍免疫细胞化学程序。我们采用了一种改良的高锰酸钾/草酸黑色素漂白技术,该技术漂白时间大幅缩短,以便在与一抗孵育前去除黑色素颗粒。我们评估了一组适用于评估黑素细胞性病变的抗体,此外还评估了可能在研究中更有用的抗体。该研究试图确定哪些抗原可能受漂白影响,哪些不受影响。抗原S100、HMB 45、NKIC3、CD34和L26相对不受该程序影响。因子VIII相关抗原、波形蛋白和CD68抗原染色增强。相反,抗原CD3、CD31和CD45RO消失。此外,平滑肌肌动蛋白和结蛋白抗原显示出相当多的非特异性背景染色,在本研究中不可靠。该技术表明,漂白后相当广泛的抗原得以保留,并且使用传统免疫细胞化学显色剂3,3-二氨基联苯胺,无需复杂的复染,就可以可靠地区分黑素细胞和噬黑素细胞。