Sacchi N, LeBien T V, Trost S, Breviario D, Bollum F J
Cell Immunol. 1984 Mar;84(1):65-73. doi: 10.1016/0008-8749(84)90077-7.
The genomic analysis of four non-T-leukemic lines NALM-1, KM-3, NALL-1, and NALM-16 shows a rearranged configuration of the immunoglobulin mu chain genes, indicating that they represent early B stages of differentiation. The differentiative potential of these pre-B cell lines was tested using the phorbol ester tumor promoter 12-O-tetradecanoyl phorbol-13-acetate (TPA). Phenotypic changes in the immunological marker profile (induction of BA-1 and BA-2 antigens) are observed, presumably reflecting events occurring in precursor B cells. However, no maturation to immunoglobulin mu chain production could be obtained. The limited maturation can be explained on the basis of possible aberrant mu chain gene rearrangements, or other mechanisms of a regulatory nature, preventing the transcription and/or the translation of rearranged mu chain genes.
对四种非T白血病细胞系NALM-1、KM-3、NALL-1和NALM-16进行的基因组分析显示,免疫球蛋白μ链基因呈重排构型,表明它们代表早期B细胞分化阶段。使用佛波酯肿瘤启动子12-O-十四酰佛波醇-13-乙酸酯(TPA)测试了这些前B细胞系的分化潜能。观察到免疫标志物谱的表型变化(BA-1和BA-2抗原的诱导),推测反映了前体B细胞中发生的事件。然而,未能实现向免疫球蛋白μ链产生的成熟。有限的成熟可以基于可能异常的μ链基因重排或其他调节性质的机制来解释,这些机制阻止了重排的μ链基因的转录和/或翻译。