Estrogen Receptor Alpha Signaling Is Responsible for the Female Sex Bias in the Loss of Tolerance and Immune Cell Activation Induced by the Lupus Susceptibility Locus Sle1b

• Published in: Frontiers in immunology 2020-11, Vol.11, p.582214-582214
• Main Authors: Graham, Jared H, Yoachim, Shayla D, Gould, Karen A
• Format: Article
• Language: English
• Subjects: Animals; B cell activation; B-Lymphocytes - immunology; Chromatin - genetics; Chromatin - immunology; estrogen receptor; Estrogen Receptor alpha - genetics; Estrogen Receptor alpha - immunology; Female; Genetic Predisposition to Disease - genetics; Germinal Center - immunology; immune tolerance; Immune Tolerance - genetics; Immune Tolerance - immunology; Immunology; lupus; Lupus Nephritis - genetics; Lupus Nephritis - immunology; Lymphocyte Activation - genetics; Lymphocyte Activation - immunology; Male; Mice; Mice, Inbred C57BL; Phenotype; sex bias; Signal Transduction - genetics; Signal Transduction - immunology
• ISSN: 1664-3224; 1664-3224
• DOI: 10.3389/fimmu.2020.582214

The dramatic female sex bias observed in human lupus is thought to be due, at least in part, to estrogens. Using mouse models, we have shown that estrogens, acting through estrogen receptor alpha (ERα) promote lupus development and contribute significantly to the female sex bias observed in this disease. C57Bl/6 (B6) mice carrying the lupus susceptibility locus locus exhibit immune cell hyperactivation and loss of tolerance, and the action of displays a strong female sex bias. Previously, we showed that disruption of ERα completely eliminates the female sex bias in the effects of . Here we report that ERα signaling selectively modulates the action of , one of the three subloci that together constitute . We observed that disruption of ERα signaling attenuated T cell hyperactivation, formation of spontaneous germinal centers, loss of tolerance, and the development of anti-chromatin autoantibodies in B6. female mice, but had no impact on these phenotypes in B6. male mice. In fact, disruption of ERα completely abolished the female sex bias that is seen in each of these phenotypes in B6. mice. Strikingly, -induced B cell hyperactivation, a female sex-specific manifestation of , was completely abrogated by disruption of ERα in B6. females. Altogether, these results demonstrate that ERα signaling is responsible for the female sex bias in the actions of , and is absolutely required for the female-specific B cell hyperactivation phenotype associated with this lupus susceptibility locus. By contrast, we found that ERα signaling had no impact on , the other sublocus that exerts effects that show a female sex bias.