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The immune synapse clears and excludes molecules above a size threshold

Author

Listed:
  • Adam N. R. Cartwright

    (Manchester Collaborative Centre for Inflammation Research, University of Manchester
    Imperial College London)

  • Jeremy Griggs

    (GlaxoSmithKline)

  • Daniel M. Davis

    (Manchester Collaborative Centre for Inflammation Research, University of Manchester)

Abstract

Natural killer cells assess target cell health via interactions at the immune synapse (IS) that facilitates signal integration and directed secretion. Here we test whether the IS also functions as a gasket. Quantitative fluorescence microscopy of nanometer-scale dextrans within synapses formed by various effector-target cell conjugates reveal that molecules are excluded in a size-dependent manner at activating synapses. Dextran sized ≤4 nm move in and out of the IS, but access is significantly reduced (by >50%) for dextran sized 10–13 nm, and dextran ≥32 nm is almost entirely excluded. Depolymerization of F-actin abrogated exclusion. Unexpectedly, larger-sized dextrans are cleared as the IS assembles in a zipper-like manner. Monoclonal antibodies are also excluded from the IS but smaller single-domain antibodies are able to penetrate. Therefore, the IS can clear and exclude molecules above a size threshold, and drugs designed to target synaptic cytokines or cytotoxic proteins must fit these dimensions.

Suggested Citation

  • Adam N. R. Cartwright & Jeremy Griggs & Daniel M. Davis, 2014. "The immune synapse clears and excludes molecules above a size threshold," Nature Communications, Nature, vol. 5(1), pages 1-13, December.
  • Handle: RePEc:nat:natcom:v:5:y:2014:i:1:d:10.1038_ncomms6479
    DOI: 10.1038/ncomms6479
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    Cited by:

    1. Sayedali Shetab Boushehri & Katharina Essig & Nikolaos-Kosmas Chlis & Sylvia Herter & Marina Bacac & Fabian J. Theis & Elke Glasmacher & Carsten Marr & Fabian Schmich, 2023. "Explainable machine learning for profiling the immunological synapse and functional characterization of therapeutic antibodies," Nature Communications, Nature, vol. 14(1), pages 1-16, December.

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