期刊
NATURE IMMUNOLOGY
卷 13, 期 12, 页码 1171-+出版社
NATURE PUBLISHING GROUP
DOI: 10.1038/ni.2468
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- National Health and Medical Research Council of Australia
- Cancer Australia
- Cure Cancer Australia Foundation
- US National Institutes of Health [AI040310]
- Howard Hughes Medical Institute
The development and function of natural killer (NK) cells is regulated by the interaction of inhibitory receptors of the Ly49 family with distinct peptide-laden major histocompatibility complex (MHC) class I molecules, although whether the Ly49 family is able bind to other MHC class I-like molecules is unclear. Here we found that the prototypic inhibitory receptor Ly49A bound the highly conserved nonclassical MHC class I molecule H2-M3 with an affinity similar to its affinity for H-2D(d). The specific recognition of H2-M3 by Ly49A regulated the 'licensing' of NK cells and mediated 'missing-self' recognition of H2-M3-deficient bone marrow. Host peptide-H2-M3 was required for optimal NK cell activity against experimental metastases and carcinogenesis. Thus, nonclassical MHC class I molecules can act as cognate ligands for Ly49 molecules. Our results provide insight into the various mechanisms that lead to NK cell tolerance.
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