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Real-time analysis of T cell receptors in naive cells in vitro and in vivo reveals flexibility in synapse and signaling dynamics.

The real-time dynamics of the T cell receptor (TCR) reflect antigen detection and T cell signaling, providing valuable insight into the evolving events of the immune response. Despite considerable advances in studying TCR dynamics in simplified systems in vitro, live imaging of subcellular signaling complexes expressed at physiological densities in intact tissues has been challenging. In this study, we generated a transgenic mouse with a TCR fused to green fluorescent protein to provide insight into the early signaling events of the immune response. To enable imaging of TCR dynamics in naive T cells in the lymph node, we enhanced signal detection of the fluorescent TCR fusion protein and used volumetric masking with a second fluorophore to mark the T cells expressing the fluorescent TCR. These in vivo analyses and parallel experiments in vitro show minimal and transient incorporation of TCRs into a stable central supramolecular activating cluster (cSMAC) structure but strong evidence for rapid, antigen-dependent TCR internalization that was not contingent on T cell motility arrest or cSMAC formation. Short-lived antigen-independent TCR clustering was also occasionally observed. These in vivo observations demonstrate that varied TCR trafficking and cell arrest dynamics occur during early T cell activation.

Pubmed ID: 21041455


  • Friedman RS
  • Beemiller P
  • Sorensen CM
  • Jacobelli J
  • Krummel MF


The Journal of experimental medicine

Publication Data

November 22, 2010

Associated Grants

  • Agency: NCRR NIH HHS, Id: 1R21RR024895
  • Agency: NIAID NIH HHS, Id: R01 AI052116

Mesh Terms

  • Animals
  • Dendritic Cells
  • Fluorescence
  • Immunological Synapses
  • Lymphocyte Activation
  • Mice
  • Mice, Inbred C57BL
  • Receptors, Antigen, T-Cell
  • Signal Transduction