NKG7 - regulating endosomal pathways?
- PMID: 33016375
- DOI: 10.1111/imcb.12403
NKG7 - regulating endosomal pathways?
Abstract
Ng et al. have identified NKG7 as a regulator of inflammation in response to diverse immunological challenges. While NKG7 was required for the degranulation of cytotoxic cells, additional defects including reduced expansion and trafficking of CD8 T cells, and altered antigen presentation, were noted in NKG7-deficient mice. The precise mechanism by which NKG7 mediates its effects has not been resolved but may involve regulation of endosomal vesicle trafficking.
© 2020 Australian and New Zealand Society for Immunology Inc.
Comment on
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The NK cell granule protein NKG7 regulates cytotoxic granule exocytosis and inflammation.Nat Immunol. 2020 Oct;21(10):1205-1218. doi: 10.1038/s41590-020-0758-6. Epub 2020 Aug 24. Nat Immunol. 2020. PMID: 32839608 Free PMC article.
References
REFERENCES
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- Ng SS, De Labastida Rivera F, Yan JM, et al. The NK cell granule protein NKG7 regulates cytotoxic granule exocytosis and inflammation. Nat Immunol 2020; https://doi.org/10.1038/s41590-020-0758-6. Online ahead of print.
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- Turman MA, Yabe T, McSherry C, Bach FH, Houchins JP. Characterization of a novel gene (NKG7) on human chromosome 19 that is expressed in natural killer cells and T cells. Hum Immunol 1993; 36: 34-40.
-
- Medley QG, Kedersha N, O'Brien S, et al. Characterization of GMP-17, a granule membrane protein that moves to the plasma membrane of natural killer cells following target cell recognition. Proc Natl Acad Sci USA 1996; 93: 685-689.
-
- Zaunders JJ, Dyer WB, Wang B, et al. Identification of circulating antigen-specific CD4+ T lymphocytes with a CCR5+, cytotoxic phenotype in an HIV-1 long-term nonprogressor and in CMV infection. Blood 2004; 103: 2238-2247.
-
- van Es LA, de Heer E, Vleming LJ, et al. GMP-17-positive T-lymphocytes in renal tubules predict progression in early stages of IgA nephropathy. Kidney Int 2008; 73: 1426-1433.
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