Sutton V R, Wijffels G L, Walker I D, Hogarth P M, McKenzie I F
Department of Pathology, University of Melbourne, Parkville, Victoria, Australia.
J Immunogenet. 1987 Feb;14(1):43-57. doi: 10.1111/j.1744-313x.1987.tb00362.x.
Three allele-specific monoclonal antibodies to Pgp-1 (Ly-24) were used to biochemically characterize the cell surface structures with which they reacted and to map the gene(s) coding for these antigens. The targets of these three monoclonal antibodies (mAb) were shown to be encoded by a gene situated on chromosome 2 close to beta 2m [gene order (Pgp-1-beta 2m-a)] and no recombination between the loci detected by the three antibodies was revealed by genetic analysis. The genetic mapping of loci and tissue distribution of these antigens suggested that they might all correspond to a particular allelic form of the mouse phagocyte glycoprotein-1 (Pgp-1) antigen. Biochemical and serological analysis confirmed that this was indeed the case and revealed that all three mAbs were directed to one epitope. It is surprising that the tissue distribution defined by one mAb (Ly-24A) was different from that for the two other (Ly-24B) antibodies, despite the serological and biochemical identity of their respective targets. The possible reason for this unusual finding is discussed.
使用三种针对Pgp-1(Ly-24)的等位基因特异性单克隆抗体对与其反应的细胞表面结构进行生化特性分析,并对编码这些抗原的基因进行定位。这三种单克隆抗体(mAb)的靶标显示由位于2号染色体上靠近β2m的一个基因编码[基因顺序为(Pgp-1-β2m-a)],并且遗传分析未揭示三种抗体检测到的基因座之间发生重组。这些抗原的基因座遗传定位和组织分布表明,它们可能都对应于小鼠吞噬细胞糖蛋白-1(Pgp-1)抗原的一种特定等位基因形式。生化和血清学分析证实确实如此,并表明所有三种单克隆抗体都针对一个表位。令人惊讶的是,尽管一种单克隆抗体(Ly-24A)与其他两种(Ly-24B)抗体各自靶标的血清学和生化特性相同,但其定义的组织分布却有所不同。本文讨论了这一异常发现的可能原因。