Abidi S Hussain I, Dong Tao, Vuong Mai T, Sreenu Vattipally B, Rowland-Jones Sarah L, Evans Edward J, Davis Simon J
Nuffield Department of Clinical Medicine and MRC Human Immunology Unit, Weatherall Institute of Molecular Medicine, The University of Oxford, John Radcliffe Hospital, Headington, Oxford OX3 9DS, UK.
Cell Res. 2008 Jun;18(6):641-8. doi: 10.1038/cr.2008.56.
CD8 engagement with class I major histocompatibility antigens greatly enhances T-cell activation, but it is not clear how this is achieved. We address the question of whether or not the antibody-mediated ligation of CD8 alone induces transcriptional remodeling in a T-cell clone, using serial analysis of gene expression. Even though it fails to induce overt phenotypic changes, we find that CD8 ligation profoundly alters transcription in the T-cell clone, at a scale comparable to that induced by antibody-mediated ligation of CD3. The character of the resulting changes is distinct, however, with the net effect of CD8 ligation being substantially inhibitory. We speculate that ligating CD8 induces weak, T-cell receptor (TCR)-mediated inhibitory signals reminiscent of the effects of TCR antagonists. Our results imply that CD8 ligation alone is incapable of activating the T-cell clone because it fails to fully induce NFAT-dependent transcription.
CD8与I类主要组织相容性抗原的结合极大地增强了T细胞的活化,但尚不清楚这是如何实现的。我们利用基因表达序列分析,探讨了单独通过抗体介导的CD8连接是否能在T细胞克隆中诱导转录重塑这一问题。尽管它未能诱导明显的表型变化,但我们发现CD8连接会深刻改变T细胞克隆中的转录,其规模与抗体介导的CD3连接所诱导的相当。然而,所产生变化的特征是不同的,CD8连接的净效应基本上是抑制性的。我们推测,连接CD8会诱导微弱的、T细胞受体(TCR)介导的抑制信号,类似于TCR拮抗剂的作用。我们的结果表明,单独连接CD8无法激活T细胞克隆,因为它不能完全诱导依赖于活化T细胞核因子(NFAT)的转录。