Taniguchi M
Gan To Kagaku Ryoho. 1986 Mar;13(3 Pt 2):826-33.
The immunological and chemical properties of melanoma antigens have been analysed by using C57BL/6-derived B16 melanoma cells. CTL was easily induced by the antigen of the melanoma cell surface, whereas soluble antigens secreted into the culture supernates worked as a specific inducer substance of suppressor T cells. Using two syngeneic monoclonal anti-melanoma antibodies (M2590, M562), we found that the melanoma antigen was composed of GM3 (NeuAc) in association with proteins with molecular weights of 31K, 58K and 80K. M2590 detected GM3, whereas M562 recognized the protein determinant. Finally, we succeeded in cloning the genomic DNA which codes for the melanoma antigen. The B16-melanoma cosmid libraries were constructed with the shuttle vector pCV103. They were infected into ED8767 E. coli and then transfected into human P36 melanoma by protoplast fusion. The transfectants were selected in the presence of mycophenolic acid, strained with FITC-M562, and selected by FACS. Total DNA was isolated from the transfectants, and the B16 genomic clones were rescued from the M562+ transfectants by in vitro packaging with lysogenic bacterial extracts. pD2-7 (34.8kb) reproducibly expressed M562 determinants in P36 human melanoma.
利用源自C57BL/6的B16黑色素瘤细胞分析了黑色素瘤抗原的免疫学和化学特性。黑色素瘤细胞表面抗原能轻易诱导细胞毒性T淋巴细胞(CTL),而分泌到培养上清液中的可溶性抗原则作为抑制性T细胞的特异性诱导物质。使用两种同基因单克隆抗黑色素瘤抗体(M2590、M562),我们发现黑色素瘤抗原由GM3(NeuAc)与分子量为31K、58K和80K的蛋白质结合而成。M2590检测GM3,而M562识别蛋白质决定簇。最后,我们成功克隆了编码黑色素瘤抗原的基因组DNA。用穿梭载体pCV103构建了B16 - 黑色素瘤黏粒文库。将它们感染ED8767大肠杆菌,然后通过原生质体融合转染到人P36黑色素瘤细胞中。在霉酚酸存在的情况下筛选转染体用异硫氰酸荧光素标记的M562染色,并通过荧光激活细胞分选术(FACS)进行筛选。从转染体中分离总DNA,并通过用溶原性细菌提取物进行体外包装从M562 +转染体中拯救出B16基因组克隆。pD2 - 7(34.8kb)在人P36黑色素瘤中可重复表达M562决定簇。