Activated, But Not Resting, T Cells Can Be Recognized and Killed by Syngeneic NK Cells
Author(s) -
Brian Rabinovich,
Jennifer Li,
John P. Shan,
Rose Hurren,
Jan Chalupny,
David Cosman,
Richard G. Miller
Publication year - 2003
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.170.7.3572
Subject(s) - nkg2d , cytotoxic t cell , microbiology and biotechnology , interleukin 21 , brefeldin a , interleukin 12 , perforin , biology , natural killer t cell , cd8 , lymphokine activated killer cell , t cell , antigen , immunology , immune system , in vitro , biochemistry , endoplasmic reticulum , golgi apparatus
We demonstrate that IL-2-activated NK cells or lymphokine-activated killer cells recognize and kill syngeneic CD4(+) and CD8(+) T cells that have been activated by APCs. Induction with APC required TCR-specific Ag, and lysis was perforin mediated. Brefeldin A, which disrupts protein transport, inhibited the sensitivity induced by activation. In BALB/c, expression of NKG2D ligands correlated with lysis and could be inhibited by brefeldin A. As well, addition of anti-NKG2D mAb to a killing assay completely abrogated lysis. Transduction of mouse NKG2D into a human NK cell line, YTSeco, conferred upon it the ability to kill activated BALB/c T cells, indicating that NKG2D is necessary for recognition. Our data provide a basis for studying a role for NK cells in T cell regulation.
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