Distinct Signatures in the Receptor Repertoire Discriminate CD56bright and CD56dim Natural Killer Cells

NK cells are phenotypically and functionally diverse lymphocytes due to variegated expression of a large array of receptors. NK-cell activity is tightly regulated through integration of receptor-derived inhibitory and activating signals. Thus, the receptor profile of each NK cell ultimately determin...

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Published in:Frontiers in immunology Vol. 11; p. 568927
Main Authors: Schwane, Vera, Huynh-Tran, Van Hung, Vollmers, Sarah, Yakup, Vivien Maria, Sauter, Jürgen, Schmidt, Alexander H, Peine, Sven, Altfeld, Marcus, Richert, Laura, Körner, Christian
Format: Journal Article
Language:English
Published: Switzerland Frontiers 01-12-2020
Frontiers Media S.A
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Summary:NK cells are phenotypically and functionally diverse lymphocytes due to variegated expression of a large array of receptors. NK-cell activity is tightly regulated through integration of receptor-derived inhibitory and activating signals. Thus, the receptor profile of each NK cell ultimately determines its ability to sense aberrant cells and subsequently mediate anti-viral or anti-tumor responses. However, an in-depth understanding of how different receptor repertoires enable distinct immune functions of NK cells is lacking. Therefore, we investigated the phenotypic diversity of primary human NK cells by performing extensive phenotypic characterization of 338 surface molecules using flow cytometry (n = 18). Our results showed that NK cells express at least 146 receptors on their surface. Of those, 136 (>90%) exhibited considerable inter-donor variability. Moreover, comparative analysis of CD56bright and CD56dim NK cells identified 70 molecules with differential expression between the two major NK-cell subsets and allowed discrimination of these subsets unsupervised hierarchical clustering. These receptors were associated with a broad range of NK-cell functions and multiple molecules were not previously associated with predominant expression on either subset (e.g. CD82 and CD147). Altogether, our study contributes to an improved understanding of the phenotypic diversity of NK cells and its potential functional implications on a cellular and population level. While the identified distinct signatures in the receptor repertoires provide a molecular basis for the differential immune functions exerted by CD56bright and CD56dim NK cells, the observed inter-individual differences in the receptor repertoire of NK cells may contribute to a diverging ability to control certain diseases.
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PMCID: PMC7736243
Reviewed by: Quirin Hammer, Karolinska Institutet (KI), Sweden; Yenan Bryceson, Karolinska Institutet (KI), Sweden
This article was submitted to NK and Innate Lymphoid Cell Biology, a section of the journal Frontiers in Immunology
Edited by: Martin R. Goodier, University of London, United Kingdom
ISSN:1664-3224
1664-3224
DOI:10.3389/fimmu.2020.568927