4.8 Article

Cytotoxic T Cells Use Mechanical Force to Potentiate Target Cell Killing

Journal

CELL
Volume 165, Issue 1, Pages 100-110

Publisher

CELL PRESS
DOI: 10.1016/j.cell.2016.01.021

Keywords

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Funding

  1. NIH [R01-AI087644, R01-AI088377, PN2-EY016586, P30-CA008748]
  2. AXA-Ecole Polytechnique Chair
  3. Labex LaSIPS MECALEUCO
  4. French National Research Agency [ANR-13-BSV2-0018]
  5. French Foundation for Medical Research [FRM DEQ20140329513]
  6. Geoffrey Beene Cancer Research Center
  7. Starr Cancer Consortium
  8. Leukemia and Lymphoma Society
  9. Agence Nationale de la Recherche (ANR) [ANR-13-BSV2-0018] Funding Source: Agence Nationale de la Recherche (ANR)

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The immunological synapse formed between a cytotoxic T lymphocyte (CTL) and an infected or transformed target cell is a physically active structure capable of exerting mechanical force. Here, we investigated whether synaptic forces promote the destruction of target cells. CTLs kill by secreting toxic proteases and the pore forming protein perforin into the synapse. Biophysical experiments revealed a striking correlation between the magnitude of force exertion across the synapse and the speed of perforin pore formation on the target cell, implying that force potentiates cytotoxicity by enhancing perforin activity. Consistent with this interpretation, we found that increasing target cell tension augmented pore formation by perforin and killing by CTLs. Our data also indicate that CTLs coordinate perforin release and force exertion in space and time. These results reveal an unappreciated physical dimension to lymphocyte function and demonstrate that cells use mechanical forces to control the activity of outgoing chemical signals.

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