Hare Katherine J, Pongracz Judit, Jenkinson Eric J, Anderson Graham
Department of Anatomy, Division of Immunity and Infection, MRC Centre for Immune Regulation, University of Birmingham B15 2TT, UK.
Immunology. 2002 Feb;105(2):163-70. doi: 10.1046/j.1365-2567.2002.01364.x.
The acquisition of functional competence represents a critical phase during intrathymic development of T cells. Thymocytes reaching this stage represent cells which have been positively selected on the basis of major histocompatibility complex reactivity, but which have also been purged of potentially autoreactive T-cell receptor specificities by negative selection. While the developmental window in which thymocytes are subjected to positive selection is now well defined, the precise developmental timing of negative selection, in relation to positive selection events, is less clear. Moreover, the underlying mechanism allowing single-positive thymocytes to respond to T-cell receptor ligation by activation rather than death, remains controversial. Here we have analysed the developmental timing of negative selection in relation to positive selection, using measurement of thymocyte susceptibility to dendritic cell presentation of the superantigen staphylococcal enterotoxin B (SEB). We show that thymocytes which have received initial positive selection signals, namely CD4+ CD8+ CD69+ thymocytes, like their CD4+ CD8+ CD69minus sign precursors, are susceptible to negative selection, indicating that induction of positive selection does not convey immediate resistance to negative selection. In contrast, newly generated CD4+ CD8minus sign CD69+ cells are not only resistant to deletion by SEB, but respond to SEB-mediated T-cell receptor-ligation by activation, indicating that the acquisition of functional competence occurs at the newly generated CD4+ CD8minus sign CD69+ stage. Finally, by using direct retroviral infection of primary CD4+ CD8+ thymocytes, we also show that Notch-1 activation in CD4+ CD8+ thymocytes does not correlate with, nor convey resistance to superantigen-mediated negative selection. Thus, our data suggest that although Notch-1 has been implicated in resistance to thymocyte apoptosis, the acquisition of resistance to negative selection occurs independently of Notch-1 signalling.
获得功能能力是T细胞胸腺内发育过程中的一个关键阶段。达到这一阶段的胸腺细胞是那些基于主要组织相容性复合体反应性而被阳性选择的细胞,但也已通过阴性选择清除了潜在的自身反应性T细胞受体特异性。虽然胸腺细胞接受阳性选择的发育窗口现已明确界定,但阴性选择相对于阳性选择事件的确切发育时间尚不清楚。此外,允许单阳性胸腺细胞通过激活而非死亡来响应T细胞受体连接的潜在机制仍存在争议。在此,我们通过测量胸腺细胞对超抗原葡萄球菌肠毒素B(SEB)树突状细胞呈递的敏感性,分析了阴性选择相对于阳性选择的发育时间。我们发现,已接收初始阳性选择信号的胸腺细胞,即CD4+CD8+CD69+胸腺细胞,与其CD4+CD8+CD69-前体一样,易受阴性选择影响,这表明阳性选择的诱导并未立即赋予对阴性选择的抗性。相反,新产生的CD4+CD8-CD69+细胞不仅对SEB介导的缺失具有抗性,而且通过激活对SEB介导的T细胞受体连接作出反应,这表明功能能力的获得发生在新产生的CD4+CD8-CD69+阶段。最后,通过对原代CD4+CD8+胸腺细胞进行直接逆转录病毒感染,我们还表明CD4+CD8+胸腺细胞中的Notch-1激活与超抗原介导的阴性选择抗性无关,也不赋予这种抗性。因此,我们的数据表明,虽然Notch-1与胸腺细胞凋亡抗性有关,但对阴性选择抗性的获得独立于Notch-1信号传导。