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Structural mechanisms of costimulation

Nature Immunology volume 3, pages 427–434 (2002)Cite this article

Abstract

Recent studies have highlighted the structural requirements for T cell costimulation and have revealed unusual modes of dimerization for the cytolytic T lymphocyte–associated antigen 4 (CTLA-4) costimulatory receptor and its B7 ligands. These distinctive quaternary structures potentially endow both receptor and ligand with bivalent binding properties, which suggests a number of mechanistic features relevant to signaling. These include the potential to form a highly ordered, alternating network of CTLA-4 and B7 homodimers that may represent the organization of these molecules and their associated signaling partners within the immunological synapse. Primary sequence and structural considerations suggest that some aspects of the organizational and mechanistic features associated with the CTLA-4–B7 complexes may extend to other members of the costimulatory receptor-ligand family. An examination of the signaling mechanisms within the costimulatory receptor-ligand family provides an excellent framework to consider the general principles that are relevant to cell surface receptor–mediated signaling events.

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Figure 1: Organization and sequences of costimulatory molecules.
Figure 2: Structure of the CTLA-4–B7 complexes.
Figure 3: Extended periodic arrays formed by the CTLA-4–B7 complexes.
Figure 4: Mechanisms of signal transduction by cell surface receptor-ligand engagement.

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Acknowledgements

We thank A. Bresnick, T. DiLorenzo and M. Scharf for helpful comments. Supported by grants from the National Institutes of Health (NIH) to S. C. A. and S. G. N.

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Author notes

  1. Jean-Claude D. Schwartz and Xuewu Zhang: These authors contributed equally to this work.

Authors and Affiliations

  1. Department of Microbiology and Immunology, Albert Einstein College of Medicine, 1300 Morris Park Ave., Bronx, 10461, NY, USA

    Jean-Claude D. Schwartz & Stanley G. Nathenson

  2. Department of Cell Biology, Albert Einstein College of Medicine, 1300 Morris Park Ave., Bronx, 10461, NY, USA

    Xuewu Zhang & Stanley G. Nathenson

  3. Department of Biochemistry, Albert Einstein College of Medicine, 1300 Morris Park Ave., Bronx, 10461, NY, USA

    Steven C. Almo

  4. Center for Synchrotron Biosciences, Albert Einstein College of Medicine, 1300 Morris Park Ave., Bronx, 10461, NY, USA

    Steven C. Almo

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Correspondence to Steven C. Almo.

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Schwartz, JC., Zhang, X., Nathenson, S. et al. Structural mechanisms of costimulation. Nat Immunol 3, 427–434 (2002). https://doi.org/10.1038/ni0502-427

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