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Published on: March 14, 2011
Inhibition of human NK cell-mediated killing by CD1 molecules
E Carbone1, G Terrazzano, A Melián
1Microbiology and Tumorbiology Center, Karolinska Institutet, Stockholm, Sweden. ennio.carbone@mtc.ki.se
Insights
Natural killer (NK) cells typically inhibit target cell lysis. This study reveals that CD1 molecules (CD1a, CD1b, CD1c) can also inhibit NK cell-mediated lysis, especially when bound to bacterial antigens.
Area of Science:
- Immunology
- Cell Biology
- Molecular Biology
Background:
- Natural killer (NK) cells recognize MHC class I molecules, inhibiting target cell lysis.
- Structural similarities exist between MHC class I and non-MHC-encoded CD1 molecules.
Purpose of the Study:
- To investigate if human CD1a, CD1b, and CD1c proteins serve as NK cell receptor targets.
- To determine the effect of CD1 expression on NK cell-mediated cytotoxicity.
Main Methods:
- Transfected NK-sensitive target cells expressing individual CD1 proteins.
- Incubation with anti-CD1 monoclonal antibodies (mAbs).
- Analysis of NK cell-mediated lysis of cultured human dendritic cells.
Main Results:
- CD1a, CD1b, or CD1c expression partially inhibited target cell lysis by human NK cells.
- Inhibitory effects were reversed by anti-CD1 mAbs.
- CD1 expression on dendritic cells also inhibited NK-mediated lysis.
- Bacterial glycolipid antigens augmented the inhibitory effects of CD1 on NK cell lysis.
Conclusions:
- CD1 molecules function as specific target structures for NK cell receptors.
- CD1-mediated inhibition of NK cell cytotoxicity is antigen-dependent.
- CD1 proteins play a role in modulating NK cell responses in vivo.
Abstract:
It is now well established that NK cells recognize classical and nonclassical MHC class I molecules and that such recognition typically results in the inhibition of target cell lysis. Given the known structural similarities between MHC class I and non-MHC-encoded CD1 molecules, we investigated the possibility that human CD1a, -b, and -c proteins might also function as specific target structures for NK cell receptors. Here we report that expression of CD1a, -b, or -c can partially inhibits target cell lysis by freshly isolated human NK cells and cultured NK lines. The inhibitory effects of CD1 molecules on NK cell could be shown upon expression of individual CD1 proteins in transfected NK-sensitive target cells, and these effects could be reversed by incubation of the target cells with mAbs specific for the expressed form of CD1. Inhibitory effects of CD1 expression on NK-mediated lysis could also be shown for cultured human dendritic cells, which represent a cell type that prominently expresses the various CD1 proteins in vivo. In addition, the bacterial glycolipid Ags known to be bound and presented by CD1 proteins could significantly augment the observed inhibitory effects on target cell lysis by NK cells.
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