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Cells in the immune and nervous systems communicate through informational synapses. The two-dimensional chemistry underlying the process of synapse formation is beginning to be explored using fluorescence imaging and mechanical techniques. Early analysis of two-dimensional kinetic rates (kon and koff) and equilibrium constants (Kd) provides a number of biological insights. First, there are two regimes for adhesion—one disordered with slow kon and the other self-ordered with 104-fold faster kon. Despite huge variation in two-dimensional kon, the two-dimensional koff is like koff in solution, and two-dimensional koff is more closely related to intrinsic properties of the interaction than the two-dimensional kon. Thus difference in koff can be used to set signaling thresholds. Early signaling complexes are compartmentalized to generate synergistic signaling domains. Immune antigen receptor components have a role in neural synapse editing. This suggests significant parallels in informational synapse formation based on common two-dimensional chemistry and signaling strategies.
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Supplemental Video. Interaction of CD2 and CD58 measured by the fluorescence method. Human T cell-like cells (Jurkat T leukemic cell line) were incubated on planar bilayers with Cy3 labeled CD58. As the cells make contact with the surface, the CD2 on the surface of the Jurkat cells engages the labeled CD58 and induces accumulation. The time lapse ratio increases from 30 times in early frames to 120 times toward the end of the sequence. Two cell contacts are visualized at a temperature of 24°C. Ordered contacts with size greater than 1 µm form within seconds of contact and undergo dynamic rearrangements and mergers over time.
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