Lee Mark S, Glassman Caleb R, Deshpande Neha R, Badgandi Hemant B, Parrish Heather L, Uttamapinant Chayasith, Stawski Philipp S, Ting Alice Y, Kuhns Michael S
Department of Immunobiology, The University of Arizona College of Medicine, Tucson, AZ 85724, USA.
Department of Immunobiology, The University of Arizona College of Medicine, Tucson, AZ 85724, USA; The Arizona Center on Aging, The University of Arizona College of Medicine, Tucson, AZ 85724, USA.
Immunity. 2015 Aug 18;43(2):227-39. doi: 10.1016/j.immuni.2015.06.018. Epub 2015 Jul 28.
The eight-subunit T cell receptor (TCR)-CD3 complex is the primary determinant for T cell fate decisions. Yet how it relays ligand-specific information across the cell membrane for conversion to chemical signals remains unresolved. We hypothesized that TCR engagement triggers a change in the spatial relationship between the associated CD3ζζ subunits at the junction where they emerge from the membrane into the cytoplasm. Using three in situ proximity assays based on ID-PRIME, FRET, and EPOR activity, we determined that the cytosolic juxtamembrane regions of the CD3ζζ subunits are spread apart upon assembly into the TCR-CD3 complex. TCR engagement then triggered their apposition. This mechanical switch resides upstream of the CD3ζζ intracellular motifs that initiate chemical signaling, as well as the polybasic stretches that regulate signal potentiation. These findings provide a framework from which to examine triggering events for activating immune receptors and other complex molecular machines.
由八个亚基组成的T细胞受体(TCR)-CD3复合物是决定T细胞命运的主要因素。然而,它如何将配体特异性信息传递过细胞膜并转化为化学信号仍未得到解决。我们推测,TCR的结合会引发相关CD3ζζ亚基在从细胞膜进入细胞质的交界处的空间关系发生变化。我们使用了基于ID-PRIME、FRET和EPOR活性的三种原位邻近分析方法,确定CD3ζζ亚基的胞质近膜区域在组装成TCR-CD3复合物时会分开。TCR的结合随后引发它们相互靠近。这种机械开关位于启动化学信号传导的CD3ζζ细胞内基序以及调节信号增强的多碱性序列的上游。这些发现提供了一个框架,据此可以研究激活免疫受体和其他复杂分子机器的触发事件。