Owen F L, Strauss W M, Murre C, Duby A D, Hiai H, Seidman J G
Proc Natl Acad Sci U S A. 1986 Oct;83(19):7434-7. doi: 10.1073/pnas.83.19.7434.
Characterization of tumors that arise spontaneously in the AKR mouse indicates that they are derived from cells of a distinct T-cell lineage. Cells in this subclass bear surface antigens, designated Tpre, Tthy, Tind, and Tsu, which are encoded by genes in the Tsu linkage group on murine chromosome 12. We have examined the rearrangement and expression of genes encoding the T-cell alpha, beta, and gamma chains in these tumors. Although these cells contain alpha-chain mRNA, they do not produce a normal-sized beta-chain mRNA. Most of them also lack gamma-chain mRNA. Each thymic leukemia was derived from a cell arrested at a different stage of development as defined by their expression of terminal deoxynucleotidyl transferase and Thy-1 mRNA. The data presented here are consistent with a model in which thymocytes expressing Tpre, Tthy, Tind, or Tsu undergo somatic development parallel to the development of other T cells. However, these thymocytes do not appear to differentiate into cells bearing alpha-beta heterodimers of the T-cell antigen receptor.
对AKR小鼠自发产生的肿瘤的特征分析表明,它们源自一个独特的T细胞谱系的细胞。该亚类中的细胞带有表面抗原,命名为Tpre、Tthy、Tind和Tsu,这些抗原由小鼠12号染色体上Tsu连锁群中的基因编码。我们已经检测了这些肿瘤中编码T细胞α、β和γ链的基因的重排和表达。尽管这些细胞含有α链mRNA,但它们不产生正常大小的β链mRNA。它们中的大多数也缺乏γ链mRNA。根据末端脱氧核苷酸转移酶和Thy-1 mRNA的表达情况,每一例胸腺白血病都源自于处于不同发育阶段停滞的细胞。此处呈现的数据与一个模型相符,在该模型中,表达Tpre、Tthy、Tind或Tsu的胸腺细胞经历与其他T细胞发育平行的体细胞发育。然而,这些胸腺细胞似乎不会分化为带有T细胞抗原受体α-β异二聚体的细胞。