Journal
FRONTIERS IN IMMUNOLOGY
Volume 12, Issue -, Pages -Publisher
FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2021.810080
Keywords
NK cell; CXCR6; tissue resident NK cells; peripheral blood NK cells; phenotypic and functional plasticity
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In this study, the distinct phenotypic profiles preserved in expanded peripheral blood NK cells were observed. The CXCR6(+) PB-NK cells became functionally equivalent to CXCR6(-) PB-NK cells after 14 days of expansion. Moreover, the CXCR6(+) PB-NK cells displayed superior antibody-dependent cellular cytotoxicity.
Human NK cells are comprised of phenotypic subsets, whose potentially unique functions remain largely unexplored. C-X-C-motif-chemokine-receptor-6 (CXCR6)(+) NK cells have been identified as phenotypically immature tissue-resident NK cells in mice and humans. A small fraction of peripheral blood (PB)-NK cells also expresses CXCR6. However, prior reports about their phenotypic and functional plasticity are conflicting. In this study, we isolated, expanded, and phenotypically and functionally evaluated CXCR6(+) and CXCR6(-) PB-NK cells, and contrasted results to bulk liver and spleen NK cells. We found that CXCR6(+) and CXCR6(-) PB-NK cells preserved their distinct phenotypic profiles throughout 14 days of in vitro expansion (day 14), after which phenotypically immature CXCR6(+) PB-NK cells became functionally equivalent to CXCR6(-) PB-NK cells. Despite a consistent reduction in CD16 expression and enhanced expression of the transcription factor Eomesodermin (Eomes), day 14 CXCR6(+) PB-NK cells had superior antibody-dependent cellular cytotoxicity (ADCC) compared to CXCR6(-) PB-NK cells. Further, bulk liver NK cells responded to IL-15, but not IL-2 stimulation, with STAT-5 phosphorylation. In contrast, bulk splenic and PB-NK cells robustly responded to both cytokines. Our findings may allow for the selection of superior NK cell subsets for infusion products increasingly used to treat human diseases.
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