Major histocompatibility complex class I-dependent skewing of the natural killer cell Ly49 receptor reportoire

Authors

  • Werner Held,

    1. Department of Molecular and Cell Biology and Cancer Research Laboratory, University of California, Berkeley, USA
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    • W. Held and J. R. Dorfman contributed equally to this study.

  • Jeffrey R. Dorfman,

    1. Department of Molecular and Cell Biology and Cancer Research Laboratory, University of California, Berkeley, USA
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    • W. Held and J. R. Dorfman contributed equally to this study.

  • Ming-Fan Wu,

    1. Department of Molecular and Cell Biology and Cancer Research Laboratory, University of California, Berkeley, USA
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  • David H. Raulet

    Corresponding author
    1. Department of Molecular and Cell Biology and Cancer Research Laboratory, University of California, Berkeley, USA
    • Department of Molecular and Cell Biology, University of California, Berkeley, CA 94720, USA, Fax: +1-510-642-1443
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Abstract

Subsets of mouse natural killer (NK) cells express receptors encoded by the Ly49 gene family that recognize allelic determinants on major histocompatibility complex (MHC) class I molecules. Recognition of self class I molecules typically inhibits NK cell lytic function. The presence of NK cell subsets expressing receptors which are able to discriminate class I alleles raises the possibility that there exist mechanisms to coordinate the NK cell receptor repertoire with the class I molecules of the host. In the present study, we determined the effects of class I gene expression on the frequencies of NK cells expressing three different Ly49 receptors defined by monoclonal antibodies. We show here an MHC-dependent skewing of NK cell subsets expressing multiple Ly49 receptors with specificity for self MHC. The results provide the first evidence that the frequencies of NK cells expressing different Ly49 receptors are determined by the host's MHC molecules. The results also extend previous findings that MHC class I expression influences the cell surface levels of each Ly49 receptor, suggesting an additional mechanism by which MHC molecules may influence the effective specificity of NK cells. Models to account for self tolerance and MHC-controlled repertoire differences are discussed.

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