Abstract
Natural killer cells are able to recognize and kill target cells according to differences in MHC class I expression. In rodents, the Ly49 receptors are primarily responsible for this MHC differentiation. We previously described the cloning of a novel C-type lectin-like receptor, KLRH1, encoded in the NK complex adjacent to the Ly49 genes and expressed by subsets of NK and NKT cells. MHC influence on selection of KLRH1(+) NK cells in congenic strains suggested that KLRH1 may have an MHC ligand, although we were unable to identify any such ligand. In this study, we have used a sensitive reporter system and Fc fusion protein to demonstrate that KLRH1 binds specifically to the classical MHC class I molecule RT1-A2 of the RT1(n) haplotype. Cytolytic activity of KLRH1-transfected RNK-16 cells was also inhibited by target cells expressing RT1-A2(n). Thus, KLRH1 represents a novel family of MHC allele-specific inhibitory receptors expressed by NK cells.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Alleles
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Animals
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CHO Cells
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Cell Line
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Cricetinae
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Gene Expression
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Genes, Reporter
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Haplotypes
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Histocompatibility Antigens / genetics
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Histocompatibility Antigens / immunology*
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Histocompatibility Antigens / metabolism
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Killer Cells, Natural / cytology
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Killer Cells, Natural / immunology*
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Killer Cells, Natural / metabolism
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Ligands
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NK Cell Lectin-Like Receptor Subfamily A / genetics
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NK Cell Lectin-Like Receptor Subfamily A / immunology
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Protein Binding
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Protein Isoforms / genetics
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Protein Isoforms / immunology
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Protein Isoforms / metabolism
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Rats
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Receptors, Immunologic / genetics
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Receptors, Immunologic / immunology*
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Receptors, Immunologic / metabolism
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Recombinant Fusion Proteins / genetics
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Recombinant Fusion Proteins / immunology
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Recombinant Fusion Proteins / metabolism
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Transfection
Substances
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Histocompatibility Antigens
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Klrh1 protein, rat
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Ligands
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NK Cell Lectin-Like Receptor Subfamily A
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Protein Isoforms
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Receptors, Immunologic
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Recombinant Fusion Proteins
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histocompatibility antigens RT, rat