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dc.rights.licenseopenen_US
dc.contributor.authorSCHWANE, V.
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorHUYNH-TRAN, Van Hung
dc.contributor.authorVOLLMERS, S.
dc.contributor.authorYAKUP, V. M.
dc.contributor.authorSAUTER, J.
dc.contributor.authorSCHMIDT, A. H.
dc.contributor.authorPEINE, S.
dc.contributor.authorALTFELD, M.
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorRICHERT, Laura
dc.contributor.authorKORNER, C.
dc.date.accessioned2021-03-16T14:04:32Z
dc.date.available2021-03-16T14:04:32Z
dc.date.issued2020-12-19
dc.identifier.issn1664-3224 (Electronic) 1664-3224 (Linking)en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/26689
dc.description.abstractEnNK 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 via 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.
dc.language.isoENen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.title.enDistinct Signatures in the Receptor Repertoire Discriminate CD56bright and CD56dim Natural Killer Cells
dc.title.alternativeFront Immunolen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.3389/fimmu.2020.568927en_US
dc.subject.halSciences du Vivant [q-bio]/Santé publique et épidémiologieen_US
dc.identifier.pubmed33335526en_US
bordeaux.journalFrontiers in Immunologyen_US
bordeaux.page568927en_US
bordeaux.volume11en_US
bordeaux.hal.laboratoriesBordeaux Population Health Research Center (BPH) - U1219en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.teamSISTM_BPH
bordeaux.teamHEALTHY_BPH
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.exportfalse
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Frontiers%20in%20Immunology&rft.date=2020-12-19&rft.volume=11&rft.spage=568927&rft.epage=568927&rft.eissn=1664-3224%20(Electronic)%201664-3224%20(Linking)&rft.issn=1664-3224%20(Electronic)%201664-3224%20(Linking)&rft.au=SCHWANE,%20V.&HUYNH-TRAN,%20Van%20Hung&VOLLMERS,%20S.&YAKUP,%20V.%20M.&SAUTER,%20J.&rft.genre=article


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