Tsubata T, Tsubata R, Reth M
Max-Planck-Institut für Immunbiologie, Freiburg, Germany.
Int Immunol. 1992 Jun;4(6):637-41. doi: 10.1093/intimm/4.6.637.
We constructed an expression vector encoding a truncated Ig mu chain that lacks both VH and CH1 domains (mu delta m chain) and introduced the mu delta m vector into the Ig negative Abelson pre-B cell line P17-27. The transfectants expressed a large amount of the mu delta m chain on their surface, which was not complexed with the lambda 5 and VpreB surrogate light chain molecules. While P17-27 transfected with a vector for the intact micron chain (P17-27 micron) shows V kappa rearrangements in culture, V kappa rearrangements were not detected in P17-27 mu delta m cells. When the mu delta m chains on the cell surface were crosslinked by anti-mu antibodies, V kappa gene rearrangements were induced in P17-27 mu delta m. These results strongly suggest that crosslinking of the micron-lambda 5-VpreB complex on the pre-B cell surface generates a signal that activates V kappa gene rearrangement, and that the lambda 5 and VpreB molecules are necessary for the spontaneous crosslinking of surface Ig on pre-B cells.
我们构建了一个编码截短型Igμ链的表达载体,该μ链缺乏VH和CH1结构域(μδm链),并将μδm载体导入Ig阴性的阿贝尔森前B细胞系P17 - 27。转染细胞在其表面表达大量的μδm链,该链未与λ5和VpreB替代轻链分子形成复合物。虽然用完整μ链载体转染的P17 - 27(P17 - 27μ)在培养中显示Vκ重排,但在P17 - 27μδm细胞中未检测到Vκ重排。当细胞表面的μδm链被抗μ抗体交联时,P17 - 27μδm中诱导了Vκ基因重排。这些结果强烈表明,前B细胞表面的μ - λ5 - VpreB复合物的交联产生了激活Vκ基因重排的信号,并且λ5和VpreB分子对于前B细胞表面Ig的自发交联是必需的。