Lucas B, Vasseur F, Penit C
U.345 INSERM, CHU Necker-enfants Malades, Paris, France.
J Immunol. 1994 Jul 1;153(1):53-62.
The main steps in intrathymic T cell differentiation have been defined using bromodeoxyuridine as a postmitotic cell tracer. Thymocytes with a high surface expression of the TCR are generated in the first 24 h after DNA synthesis. The phenotype of these TCR(high) cells was studied during 10 days by using pairs of surface markers associated with BrdUrd. During the first 2 days, TCR(high) cells were of the CD4+CD8+HSA(high) phenotype, transiently expressed the early activation marker CD69, and contained a high percentage of cycling cells. This activation step preceded the transition from CD4+CD8+ to CD4+CD8- and then to CD4-CD8+ cells, followed by progressive HSA down regulation and increase in the expression of H-2K, Qa-2, and CD45RB. The phenotypic maturation was completed in 9 days. In Mls-1a mice, negative selection of V beta 6+ cells was observed at the earliest step of TCR(high) cell generation, and positive selection of V beta 8.2+ and V beta 14+ cells took place later and was correlated to the activation step. These data suggest that high TCR expression and cell activation are necessary for positive selection and subsequent T cell maturation.
胸腺内T细胞分化的主要步骤已通过使用溴脱氧尿苷作为有丝分裂后细胞示踪剂得以确定。在DNA合成后的最初24小时内产生具有高表面TCR表达的胸腺细胞。通过使用与BrdUrd相关的表面标志物对,在10天内研究了这些TCR(高)细胞的表型。在最初的2天内,TCR(高)细胞具有CD4+CD8+HSA(高)表型,短暂表达早期激活标志物CD69,并含有高比例的循环细胞。这一激活步骤先于从CD4+CD8+向CD4+CD8-,然后向CD4-CD8+细胞的转变,随后HSA逐渐下调,H-2K、Qa-2和CD45RB的表达增加。表型成熟在9天内完成。在Mls-1a小鼠中,在TCR(高)细胞产生的最早阶段观察到Vβ6+细胞的阴性选择,而Vβ8.2+和Vβ14+细胞的阳性选择发生在稍后阶段,并且与激活步骤相关。这些数据表明,高TCR表达和细胞激活对于阳性选择及随后的T细胞成熟是必要的。