Hedgehog signaling controls T cell killing at the immunological synapse

  • de la Roche M
  • Ritter A
  • Angus K
 et al. 
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Abstract

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.

Author-supplied keywords

  • *Cytotoxicity, Immunologic
  • *Immunological Synapses
  • *Signal Transduction
  • Animals
  • CD8-Positive T-Lymphocytes/*immunology/metabolism
  • Cell Polarity
  • Cells, Cultured
  • Centrosome/metabolism
  • Hedgehog Proteins/*metabolism
  • Kruppel-Like Transcription Factors/genetics/metabo
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Models, Immunological
  • Neuropeptides/genetics/metabolism
  • Receptors, Antigen, T-Cell/immunology/metabolism
  • Receptors, Cell Surface/metabolism
  • Receptors, G-Protein-Coupled/metabolism
  • T-Lymphocytes, Cytotoxic/*immunology/metabolism
  • rac1 GTP-Binding Protein/genetics/metabolism

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  • PMID: 24311692

Authors

  • M de la Roche

  • A T Ritter

  • K L Angus

  • C Dinsmore

  • C H Earnshaw

  • J F Reiter

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