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Modulation of NKG2D, NKp46, and Ly49C/I facilitates natural killer cell-mediated control of lung cancer.
- Source :
-
Proceedings of the National Academy of Sciences of the United States of America [Proc Natl Acad Sci U S A] 2018 Nov 13; Vol. 115 (46), pp. 11808-11813. Date of Electronic Publication: 2018 Oct 31. - Publication Year :
- 2018
-
Abstract
- Natural killer (NK) cells play a critical role in controlling malignancies. Susceptibility or resistance to lung cancer, for example, specifically depends on NK cell function. Nevertheless, intrinsic factors that control NK cell-mediated clearance of lung cancer are unknown. Here we report that NK cells exposed to exogenous major histocompatibility class I (MHCI) provide a significant immunologic barrier to the growth and progression of malignancy. Clearance of lung cancer is facilitated by up-regulation of NKG2D, NKp46, and other activating receptors upon exposure to environmental MHCI. Surface expression of the inhibitory receptor Ly49C/I, on the other hand, is down-regulated upon exposure to tumor-bearing tissue. We thus demonstrate that NK cells exhibit dynamic plasticity in surface expression of both activating and inhibitory receptors based on the environmental context. Our data suggest that altering the activation state of NK cells may contribute to immunologic control of lung and possibly other cancers.<br />Competing Interests: The authors declare no conflict of interest.
- Subjects :
- Animals
Cytotoxicity, Immunologic
Down-Regulation
Histocompatibility Antigens Class I metabolism
Lung Neoplasms metabolism
Mice
Mice, Inbred C57BL
Up-Regulation
Antigens, Ly immunology
Killer Cells, Natural immunology
Lung Neoplasms immunology
NK Cell Lectin-Like Receptor Subfamily A immunology
NK Cell Lectin-Like Receptor Subfamily K immunology
Natural Cytotoxicity Triggering Receptor 1 immunology
Receptors, Immunologic immunology
Receptors, Natural Killer Cell metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1091-6490
- Volume :
- 115
- Issue :
- 46
- Database :
- MEDLINE
- Journal :
- Proceedings of the National Academy of Sciences of the United States of America
- Publication Type :
- Academic Journal
- Accession number :
- 30381460
- Full Text :
- https://doi.org/10.1073/pnas.1804931115