Figure 1
The development of the immunological synapse. Images adapted from [2] based on fluorescence microscope images of T-cell interaction with agonist MHC–peptide complexes (green) and ICAM-1 (red) in a supported planar bilayer with a T cell. The accumulation of fluorescence represents interactions in different time frames. (a) Within seconds, the T cell attaches to the substrate using LFA-1/ICAM-1 interactions in the center based on TCR signaling triggered at the periphery of the contact area. (b) Over a period of minutes, the engaged TCRs are translocated to the center of the contact area. (c) The final pattern, with a central cluster of engaged TCRs surrounded by a ring of engaged LFA-1, is stable for hours. Molecular markers for the cSMAC and pSMAC are indicated. For scale, the pSMAC is ~5 μm across. ADAP, adhesion and degranulation adapter protein; cSMAC, central supramolecular activation cluster; ICAM, intercellular adhesion molecule; LFA, lymphocyte-function-associated antigen; MHCp, major histocompatibility complex protein complexed to a foreign or self-peptide; PKC-θ, a protein kinase C isoform that is activated by DAG but not Ca2+; pSMAC, peripheral supramolecular activation cluster – the ring of LFA-1 and talin on the T cell and ICAM-1 on the antigen-presenting cell in the mature immunological synapse; TCR, T-cell antigen receptor.