The Immunological Synapse

Author:

Bromley Shannon K.1234,Burack W. Richard1234,Johnson Kenneth G.1234,Somersalo Kristina1234,Sims Tasha N.1234,Sumen Cenk1234,Davis Mark M.1234,Shaw Andrey S.1234,Allen Paul M.1234,Dustin Michael L.1234

Affiliation:

1. Department of Pathology and Immunology Washington University School of Medicine, 660 S. Euclid Ave, St. Louis, Missouri 63110;

2. The Howard Hughes Medical Institute, Washington University School of Medicine, 660 S. Euclid Ave, St. Louis, Missouri 63110;

3. Department of Immunology and Microbiology Stanford University, Palo Alto, Callifornia 94305

4. The Howard Hughes Medical Institute, Stanford University, Palo Alto, Callifornia 94305

Abstract

The adaptive immune response is initiated by the interaction of T cell antigen receptors with major histocompatibility complex molecule-peptide complexes in the nanometer scale gap between a T cell and an antigen-presenting cell, referred to as an immunological synapse. In this review we focus on the concept of immunological synapse formation as it relates to membrane structure, T cell polarity, signaling pathways, and the antigen-presenting cell. Membrane domains provide an organizational principle for compartmentalization within the immunological synapse. T cell polarization by chemokines increases T cell sensitivity to antigen. The current model is that signaling and formation of the immunological synapse are tightly interwoven in mature T cells. We also extend this model to natural killer cell activation, where the inhibitory NK synapse provides a striking example in which inhibition of signaling leaves the synapse in its nascent, inverted state. The APC may also play an active role in immunological synapse formation, particularly for activation of naïve T cells.

Publisher

Annual Reviews

Subject

Immunology,Immunology and Allergy

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