4.8 Article

Hedgehog Signaling Controls T Cell Killing at the Immunological Synapse

Journal

SCIENCE
Volume 342, Issue 6163, Pages 1247-1250

Publisher

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.1244689

Keywords

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Funding

  1. Wellcome Trust [075880]
  2. Wellcome Trust Strategic Award for core facilities at the CIMR [100140]
  3. NIH [R01AR05439, R01GM095941]
  4. Burroughs Wellcome Fund
  5. David and Lucile F. Packard Foundation
  6. Sandler Family Supporting Foundation

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The centrosome is essential for cytotoxic T lymphocyte (CTL) function, contacting the plasma membrane and directing cytotoxic granules for secretion at the immunological synapse. Centrosome docking at the plasma membrane also occurs during cilia formation. The primary cilium, formed in nonhematopoietic cells, is essential for vertebrate Hedgehog (Hh) signaling. Lymphocytes do not form primary cilia, but we found and describe here that Hh signaling played an important role in CTL killing. T cell receptor activation, which prearms CTLs with cytotoxic granules, also initiated Hh signaling. Hh pathway activation occurred intracellularly and triggered Rac1 synthesis. These events prearmed CTLs for action by promoting the actin remodeling required for centrosome polarization and granule release. Thus, Hh signaling plays a role in CTL function, and the immunological synapse may represent a modified cilium.

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