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    In epithelial cells, these three molecules appear to interact with each other, are required for apical/basal polarity, and are localized to the basal/lateral membrane (Qin et al. Early in synapse formation, Scrb and Dlg are recruited to the synapse but at later time-points, they end up localized to the membrane distal to the synapse (Ludford-Menting et al. Inhibition of Scrb expression blocks motility and conjugate formation but the mechanism is not known. Although this pattern does not appear to be a universal feature of immunological synapses (Brossard et al. 2008), its distinct structure has served as a central focus of researchers in the field. The incorporation of mobile ligands into lipid bilayers has allowed the reorganization of surface receptors during T-cell activation to be visualized in real-time and with optimal resolution (Grakoui et al. In contrast, the reorganization of TCRs and integrins into p SMACs and c SMACs does not occur in systems using antibody coated glass (Bunnell et al. In addition, the highly sensitive TIRFM method allows individual molecules or small clusters of molecules to be imaged (Varma et al. Antigen induces the formation of small TCR microclusters on the order of 11–17 TCRs per microcluster (Varma et al. Although the TCR microclusters can also include molecules like CD2, CD4, CD8, and CD28, they exclude the tyrosine phosphatase CD45 (Varma et al. 2008), a step that may be important for TCR triggering (Choudhuri et al. Interestingly, LFA-1 also forms microclusters in the d SMAC that are segregated from the TCR microclusters (Kaizuka et al. Although both TCR and LFA-1 microclusters then move centripetally through the p SMAC (Kaizuka et al. In the case of the actin dependent LFA-1 clusters, one idea is that they disperse when they reach F-actin free c SMAC (Kaizuka et al. This model postulates that the c SMAC is a container that collects cargo that falls off the actinomyosin conveyor belt as it reaches the border of the p SMAC and the c SMAC.