Valitutti S, Müller S, Dessing M, Lanzavecchia A
Basel Institute for Immunology, Switzerland.
Eur J Immunol. 1996 Sep;26(9):2012-6. doi: 10.1002/eji.1830260907.
We have previously demonstrated that in T cell-antigen-presenting cell (APC) conjugates many T cell receptors (TCR) are serially triggered by a few peptide-MHC complexes, resulting in sustained signaling. Here, we investigate the mechanisms that determine the duration and extent of signaling. We show that in the course of the T helper cell-APC interaction, down-regulation of triggered TCR leads to extinction of signaling. However, T cells that have been activated by a previous encounter with peptide-pulsed APC and have extinguished signaling can swiftly repolarize towards APC displaying higher antigen concentrations and dedicate their help to these cells. These results demonstrate that TCR down-regulation allows T cells to calibrate their response and dedicate their help to APC offering the highest stimulus.
我们之前已经证明,在T细胞-抗原呈递细胞(APC)结合物中,许多T细胞受体(TCR)会被少数肽-MHC复合物连续触发,从而产生持续的信号传导。在此,我们研究决定信号传导持续时间和程度的机制。我们发现,在辅助性T细胞与APC相互作用的过程中,被触发的TCR的下调会导致信号传导的终止。然而,之前与肽脉冲APC相遇而被激活且信号传导已终止的T细胞,可以迅速重新极化,朝向展示更高抗原浓度的APC,并为这些细胞提供辅助。这些结果表明,TCR下调使T细胞能够校准其反应,并为提供最高刺激的APC提供辅助。