Suppr超能文献

前B细胞表面免疫球蛋白(μ替代轻链复合物)的交联诱导免疫球蛋白κ基因座处V基因重排的激活。

Crosslinking of the cell surface immunoglobulin (mu-surrogate light chains complex) on pre-B cells induces activation of V gene rearrangements at the immunoglobulin kappa locus.

作者信息

Tsubata T, Tsubata R, Reth M

机构信息

Max-Planck-Institut für Immunbiologie, Freiburg, Germany.

出版信息

Int Immunol. 1992 Jun;4(6):637-41. doi: 10.1093/intimm/4.6.637.

Abstract

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.

摘要

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。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验