Estrogen-mediated downregulation of AIRE influences sexual dimorphism in autoimmune diseases

Nadine Dragin(Centre de Recherche en Myologie), Jacky Bismuth(Institut de Myologie), Géraldine Cizeron-Clairac, Maria Grazia Biferi(Centre National de la Recherche Scientifique), Claire Berthault(Sorbonne Paris Cité), Alain Serraf, Rémi Nottin, David Klatzmann, Ana Cumano, Martine Barkats(Université Paris Cité), Rozen Le Panse(Centre de Recherche en Myologie), Sonia Berrih‐Aknin(Centre National de la Recherche Scientifique)
Journal of Clinical Investigation
March 20, 2016
Cited by 198Open Access
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Abstract

Autoimmune diseases affect 5% to 8% of the population, and females are more susceptible to these diseases than males. Here, we analyzed human thymic transcriptome and revealed sex-associated differences in the expression of tissue-specific antigens that are controlled by the autoimmune regulator (AIRE), a key factor in central tolerance. We hypothesized that the level of AIRE is linked to sexual dimorphism susceptibility to autoimmune diseases. In human and mouse thymus, females expressed less AIRE (mRNA and protein) than males after puberty. These results were confirmed in purified murine thymic epithelial cells (TECs). We also demonstrated that AIRE expression is related to sexual hormones, as male castration decreased AIRE thymic expression and estrogen receptor α-deficient mice did not show a sex disparity for AIRE expression. Moreover, estrogen treatment resulted in downregulation of AIRE expression in cultured human TECs, human thymic tissue grafted to immunodeficient mice, and murine fetal thymus organ cultures. AIRE levels in human thymus grafted in immunodeficient mice depended upon the sex of the recipient. Estrogen also upregulated the number of methylated CpG sites in the AIRE promoter. Together, our results indicate that in females, estrogen induces epigenetic changes in the AIRE gene, leading to reduced AIRE expression under a threshold that increases female susceptibility to autoimmune diseases.


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