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dc.rights.licenseopenen_US
dc.contributor.authorHAGEN, S. H.
dc.contributor.authorHENSELING, F.
dc.contributor.authorHENNESEN, J.
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorSAVEL, Helene
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorDELAHAYE, Solenne
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorRICHERT, Laura
dc.contributor.authorZIEGLER, S. M.
dc.contributor.authorALTFELD, M.
dc.date.accessioned2021-03-16T13:25:39Z
dc.date.available2021-03-16T13:25:39Z
dc.date.issued2020-12-08
dc.identifier.issn2211-1247 (Electronic)en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/26683
dc.description.abstractEnImmune responses differ between women and men, and type I interferon (IFN) responses following Toll-like receptor 7 (TLR7) stimulation are higher in women. The precise mechanisms driving these sex differences in immunity are unknown. To investigate possible genetic factors, we quantify escape from X chromosome inactivation (XCI) for TLR7 and four other genes (RPS6KA3, CYBB, BTK, and IL13RA1) at the single plasmacytoid dendritic cell (pDC) level. We observe escape from XCI for all investigated genes, leading to biallelic expression patterns. pDCs with biallelic gene expression have significantly higher mRNA levels of the respective genes. Unstimulated pDCs with biallelic TLR7 expression exhibit significantly higher IFNalpha/beta mRNA levels, and IFNalpha exposure results in significantly increased IFNalpha/beta protein production by pDCs. These results identify unanticipated heterogeneity in escape from XCI of several genes in pDCs and highlight the important contribution of X chromosome factors to sex differences in type I IFN responses, which might explain observed sex differences in human diseases.
dc.language.isoENen_US
dc.title.enHeterogeneous Escape from X Chromosome Inactivation Results in Sex Differences in Type I IFN Responses at the Single Human pDC Level
dc.title.alternativeCell Repen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1016/j.celrep.2020.108485en_US
dc.subject.halSciences du Vivant [q-bio]/Santé publique et épidémiologieen_US
dc.identifier.pubmed33296655en_US
bordeaux.journalCell Reportsen_US
bordeaux.page108485en_US
bordeaux.volume33en_US
bordeaux.hal.laboratoriesBordeaux Population Health Research Center (BPH) - U1219en_US
bordeaux.issue10en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.teamSISTMen_US
bordeaux.teamSISTM_BPH
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.exportfalse
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