Haustein D, Von der Ahe D
Eur J Immunol. 1986 Jan;16(1):113-5. doi: 10.1002/eji.1830160122.
Four cloned continuously cultured mouse B lymphoma cells of the lines WEHI-279, BCL1 and 38C-13 were used to study the surface presentation of IgM. Cells of all lines expose, in addition to mu 2L2, various, disulfide-linked subunits as already shown for normal B lymphocytes (Koch, N. and Haustein, D., Mol. Immunol. 1982. 19:477). In contrast to normal B cells, B lymphoma cells also carry IgM structures of higher molecular weight than mu 2L2 on their surface. Furthermore, B lymphoma cells of all investigated lines expose a mu 2L2 structure to which a 30-kDa protein is disulfide-linked. This 30-kDa protein could also be identified on normal mouse B lymphocytes when more drastic conditions were employed. mu 2L2 disulfide linked to this 30-kDa protein is the main IgM structure on normal and neoplastic B cells whereas only small amounts of mu 2L2 (unlinked to this protein) can be detected.
利用4种克隆的、连续培养的小鼠B淋巴瘤细胞系(WEHI-279、BCL1和38C-13)来研究IgM的表面呈现。除了μ2L2之外,所有细胞系的细胞都暴露有各种二硫键连接的亚基,这正如正常B淋巴细胞所显示的那样(科赫,N.和豪斯汀,D.,《分子免疫学》,1982年,19卷:477页)。与正常B细胞不同的是,B淋巴瘤细胞表面还带有分子量高于μ2L2的IgM结构。此外,所有研究细胞系的B淋巴瘤细胞都暴露有一个μ2L2结构,一个30 kDa的蛋白质通过二硫键与之相连。当采用更严格的条件时,在正常小鼠B淋巴细胞上也能鉴定出这种30 kDa的蛋白质。与该30 kDa蛋白质二硫键连接的μ2L2是正常和肿瘤性B细胞上的主要IgM结构,而只能检测到少量(未与该蛋白质连接的)μ2L2。