Egerton M, Scollay R
Walter and Eliza Hall Institute of Medical Research, Royal Parade, Parkville, Australia.
Int Immunol. 1990;2(2):157-63. doi: 10.1093/intimm/2.2.157.
The CD4-CD8- thymocyte population contains the precursors of all other thymocytes. However, it also contains a significant proportion of cells which express surface TCR alpha beta, and have little or no precursor activity. Like peripheral T cells, but unlike most other thymocytes, these TCR alpha beta+CD4-CD8- thymocytes do not express heat stable antigen. Both the origin and developmental status of these cells are unclear, and are the subject of this report. We have measured the proportion of V beta 8.1+ cells amongst TCR+HSA-CD4-CD8- thymocytes in MIs-1a versus MIs-1b mice, in order to determine whether they have undergone negative selection. The proportions were similar in both strains, in contrast to mature T cells, indicating that neither they nor their precursors had undergone clonal deletion. We also measured the accumulation of these cells over the early life of the animal and found that it was extremely slow. Our data also show that although TCR-V beta 8.1+ cells are reactive to MIs-1a in association with MHC class II, most mature TCR-V beta 8.1+ cells in MIs-1b mice are CD8+, suggesting an additional reactivity with MHC class I. We raise the possibility that TCR-V beta 8.1+CD4-CD8- thymocytes are derived from TCR-V beta 8.1+CD4+CD8+ thymocytes, and that the reactivity of TCR-V beta 8.1 with both MHC classes I and II has resulted in the down-regulation of both CD4 and CD8.
CD4-CD8-胸腺细胞群体包含所有其他胸腺细胞的前体。然而,它也包含相当比例的细胞,这些细胞表达表面TCRαβ,且几乎没有或完全没有前体活性。与外周T细胞一样,但与大多数其他胸腺细胞不同,这些TCRαβ+CD4-CD8-胸腺细胞不表达热稳定抗原。这些细胞的起源和发育状态尚不清楚,是本报告的主题。我们测量了MIs-1a与MIs-1b小鼠中TCR+HSA-CD4-CD8-胸腺细胞中Vβ8.1+细胞的比例,以确定它们是否经历了阴性选择。与成熟T细胞相反,两种品系中的比例相似,这表明它们及其前体均未经历克隆缺失。我们还测量了这些细胞在动物早期生命中的积累情况,发现其极其缓慢。我们的数据还表明,尽管TCR-Vβ8.1+细胞与MIs-1a结合MHC II类具有反应性,但MIs-1b小鼠中大多数成熟的TCR-Vβ8.1+细胞是CD8+,这表明它们与MHC I类还有额外的反应性。我们提出了TCR-Vβ8.1+CD4-CD8-胸腺细胞源自TCR-Vβ8.1+CD4+CD8+胸腺细胞的可能性,并且TCR-Vβ8.1与MHC I类和II类的反应性导致了CD4和CD8的下调。