Sugiyama H, Minami Y, Komori T, Sakato N, Kishimoto S
Third Department of Internal Medicine, Osaka University Medical School, Japan.
Immunology. 1989 Dec;68(4):453-7.
We raised anti-VH315 antibodies by immunization of rabbits with VH315 fragments, the variable portions of the immunoglobulin heavy chains of MOPC315 myeloma protein. Inhibition radioimmunoassay using various immunoglobulins as inhibitors showed that the anti-VH315 antibodies specifically reacted with the variable portions of the heavy chains of MOPC315 myeloma protein. When the variable region (VH) gene of the heavy chains was cloned and sequenced from the cells producing the heavy chains detected by the anti-VH315 antibodies, the VH gene was closely related (82% homology at amino acid level) to the VH gene of MOPC315. When we examined the frequency with which the variable region(s) detected by the anti-VH315 antibodies were expressed in eight Ignull Abelson virus-transformed cell lines (DJ/DJ or VDJ-/DJ), which were able to generate functional V regions during culture, only one cell line, AT8-1, produced a small number of intracytoplasmic mu-positive cells (VH315+ cells) stained by the anti-VH315 antibodies. The percentage of the total number of the VH315+ cells to the total number of intracytoplasmic mu-positive cells was 0.91% in AT8-1. In the remaining seven cell lines, no VH315+ cells were detected. In the present study we estimate, for the first time at the individual cell level, the frequency of the utilization of the heavy chain variable region(s) identical or closely related to that of MOPC315 in the functional V region formation during early B-cell development.
我们用VH315片段(MOPC315骨髓瘤蛋白免疫球蛋白重链的可变区)免疫兔子,制备了抗VH315抗体。使用各种免疫球蛋白作为抑制剂的抑制放射免疫分析表明,抗VH315抗体与MOPC315骨髓瘤蛋白重链的可变区发生特异性反应。当从产生抗VH315抗体所检测到的重链的细胞中克隆并测序重链的可变区(VH)基因时,该VH基因与MOPC315的VH基因密切相关(氨基酸水平同源性为82%)。当我们检测抗VH315抗体所检测到的可变区在8种Ig阴性阿贝尔逊病毒转化细胞系(DJ/DJ或VDJ-/DJ)中表达的频率时,这些细胞系在培养过程中能够产生功能性V区,结果只有一个细胞系AT8-1产生了少量被抗VH315抗体染色的胞质内μ阳性细胞(VH315+细胞)。在AT8-1中,VH315+细胞总数占胞质内μ阳性细胞总数的百分比为0.91%。在其余7个细胞系中,未检测到VH315+细胞。在本研究中,我们首次在单个细胞水平上估计了在早期B细胞发育过程中功能性V区形成过程中与MOPC315相同或密切相关的重链可变区的利用频率。