Bachmann M F, Salzmann M, Oxenius A, Ohashi P S
Ontario Cancer Institute, Department of Medical Biophysics, Toronto, Canada.
Eur J Immunol. 1998 Aug;28(8):2571-9. doi: 10.1002/(SICI)1521-4141(199808)28:08<2571::AID-IMMU2571>3.0.CO;2-T.
T cell activation involves specific interactions between the TCR and peptides presented by the MHC. This engagement leads to phosphorylation and subsequent internalization of the TCR complex. By analyzing the kinetics of the internalization of TCR, we found that the rate of TCR down-regulation was proportional to the square of the TCR density. Mathematical modeling of TCR interactions indicates that such a relation is only possible if TCR dimerize before internalization. By mathematical analysis, our data would also be compatible with trimer but not larger oligomer formation. Thus, minimal TCR oligomerization is an essential step for peptide-mediated T cell activation.
T细胞活化涉及TCR与MHC呈递的肽之间的特异性相互作用。这种结合导致TCR复合物的磷酸化及随后的内化。通过分析TCR内化的动力学,我们发现TCR下调的速率与TCR密度的平方成正比。TCR相互作用的数学模型表明,只有当TCR在内化前二聚化时,这种关系才有可能成立。通过数学分析,我们的数据也与三聚体而非更大的寡聚体形成相兼容。因此,最小限度的TCR寡聚化是肽介导的T细胞活化的关键步骤。