ORAI1-mediated calcium influx is required for human cytotoxic lymphocyte degranulation and target cell lysis

Proc Natl Acad Sci U S A. 2011 Feb 22;108(8):3324-9. doi: 10.1073/pnas.1013285108. Epub 2011 Feb 7.

Abstract

Lymphocytes mediate cytotoxicity by polarized release of the contents of cytotoxic granules toward their target cells. Here, we have studied the role of the calcium release-activated calcium channel ORAI1 in human lymphocyte cytotoxicity. Natural killer (NK) cells obtained from an ORAI1-deficient patient displayed defective store-operated Ca(2+) entry (SOCE) and severely defective cytotoxic granule exocytosis leading to impaired target cell lysis. Similar findings were obtained using NK cells from a stromal interaction molecule 1-deficient patient. The defect occurred at a late stage of the signaling process, because activation of leukocyte functional antigen (LFA)-1 and cytotoxic granule polarization were not impaired. Moreover, pharmacological inhibition of SOCE interfered with degranulation and target cell lysis by freshly isolated NK cells and CD8(+) effector T cells from healthy donors. In addition to effects on lymphocyte cytotoxicity, synthesis of the chemokine macrophage inflammatory protein-1β and the cytokines TNF-α and IFN-γ on target cell recognition was impaired in ORAI1-deficient NK cells, as previously described for T cells. By contrast, NK cell cytokine production induced by combinations of IL-12, IL-15, and IL-18 was not impaired by ORAI1 deficiency. Taken together, these results identify a critical role for ORAI1-mediated Ca(2+) influx in granule exocytosis for lymphocyte cytotoxicity as well as for cytokine production induced by target cell recognition.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Calcium / immunology*
  • Calcium Channels / immunology*
  • Cell Degranulation / immunology*
  • Chemokine CCL4 / biosynthesis
  • Cytokines / biosynthesis*
  • Cytotoxicity, Immunologic*
  • Humans
  • Interferon-gamma / biosynthesis
  • Interleukins / biosynthesis
  • Killer Cells, Natural / pathology
  • ORAI1 Protein
  • T-Lymphocytes, Cytotoxic / immunology*
  • Tumor Necrosis Factor-alpha / biosynthesis

Substances

  • Calcium Channels
  • Chemokine CCL4
  • Cytokines
  • Interleukins
  • ORAI1 Protein
  • ORAI1 protein, human
  • Tumor Necrosis Factor-alpha
  • Interferon-gamma
  • Calcium