Niho Y, Shibuya T, Yamasaki K, Kimura N
Int J Cell Cloning. 1984 May;2(3):161-72.
A human myeloma cell line (KMM-56) producing lambda-light chain protein was established in vitro by cultivation of the cells in the pleural effusion obtained from a patient with IgD-lambda-myeloma. The cells proliferate in suspension and do not aggregate or attach to the culture dish. Surface marker analysis revealed that the cells were negative for E-rosette, and surface immunoglobulin. Immunoelectrophoresis, immunodiffusion, and immunofluorescence with various antibodies demonstrated no heavy chains, while lambda-light chains were detected in the cytoplasm of the cells. Using the immunodiffusion technique, only lambda-light chains were detected in the frozen and thawed cell extract, the concentrated supernatant of the cell culture, and the urine of the patient. Electron microscopic examination revealed the plasmablastoid appearance of the cells. This cell line may be useful for future studies of human immunoglobulin genes and for the material of human-human hybridoma, which could produce monoclonal human immunoglobulin.
通过在一名IgD-λ型骨髓瘤患者的胸腔积液中培养细胞,在体外建立了一种产生λ轻链蛋白的人骨髓瘤细胞系(KMM-56)。这些细胞在悬浮液中增殖,不聚集或附着于培养皿。表面标志物分析显示,这些细胞的E花环和表面免疫球蛋白呈阴性。用各种抗体进行的免疫电泳、免疫扩散和免疫荧光显示没有重链,而在细胞的细胞质中检测到λ轻链。使用免疫扩散技术,在冻融的细胞提取物、细胞培养的浓缩上清液和患者尿液中仅检测到λ轻链。电子显微镜检查显示细胞呈成浆细胞样外观。该细胞系可能对未来人类免疫球蛋白基因的研究以及对可能产生单克隆人免疫球蛋白的人-人杂交瘤的材料有用。