page 1263, have developed a novel assay that allows them to visualize the formation of these complexes in live cells.
The authors dropped live Jurkat leukemic T cells onto coverslips coated with anti-TCR antibodies, and then tracked chimeric signaling proteins as they associated with and dissociated from signaling complexes. TCR-signaling complexes develop within 15 s, and undergo dynamic assembly and disassembly throughout the process of contact formation. Initial clustering of the TCRs does not require phosphotyrosine-dependent interactions, but the formation of a functional signaling complex does. A lipid raft marker does not localize to the complexes, a result that should fan the controversy surrounding raft function in signaling.Molecules that are recruited to the complexes depart by distinct mechanisms. The adaptor protein SLP-76 exhibits a particularly striking pattern, departing TCR-rich signaling complexes in large structures that are transported along microtubules to accumulate in a novel perinuclear structure. Bunnell et al. suggest that signaling complexes are functioning as sorting structures, as molecules are recruited to the complexes from different compartments, then sent from the complexes in different ways.
Intracellular calcium elevations in the T cells begin within 12 s of contact initiation, suggesting that a single TCR cluster may be sufficient to produce calcium elevation. TCR clusters may therefore constitute “proto-synapses” capable of directing T cell activation, a model that may explain how some types of T cells are activated without the formation of well-defined immune synapses. The authors are now extending their assay to include more markers to characterize the process of complex formation in greater detail. ▪