The Journal of Immunology · 2015 · 248 citations · 59 references
Life SciencesImmunologyMolecular BiologyInflammationInnate ImmunitySignal TransductionCytokine BiologyDendritic Cell BiologyInnate Immune ActivationInnate Immune ModulationInnate Immune ResponseInnate Immune Signaling PathwaysDendritic Cell Inflammatory ResponsesDendritic Cell SignalingEstrogen ImmunomodulationEstrogen Receptor SignalingEstrogen-mediated Immune ModulationPlasmacytoid Dendritic Cell Interferon ResponsesPlasmacytoid Dendritic Cell ResponsesSex Hormone Influences
Increased IFN-α production contributes to the pathogenesis of infectious and autoimmune diseases. Plasmacytoid dendritic cells (pDCs) from females produce more IFN-α upon TLR7 stimulation than pDCs from males, yet the mechanisms underlying this difference remain unclear. In this article, we show that basal levels of IFN regulatory factor (IRF) 5 in pDCs were significantly higher in females compared with males and positively correlated with the percentage of IFN-α-secreting pDCs. Delivery of recombinant IRF5 protein into human primary pDCs increased TLR7-mediated IFN-α secretion. In mice, genetic ablation of the estrogen receptor 1 (Esr1) gene in the hematopoietic compartment or DC lineage reduced Irf5 mRNA expression in pDCs and IFN-α production. IRF5 mRNA levels furthermore correlated with ESR1 mRNA levels in human pDCs, consistent with IRF5 regulation at the transcriptional level by ESR1. Taken together, these data demonstrate a critical mechanism by which sex differences in basal pDC IRF5 expression lead to higher IFN-α production upon TLR7 stimulation in females and provide novel targets for the modulation of immune responses and inflammation.
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