Back to Search Start Over

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

Authors :
Dragin N
Bismuth J
Cizeron-Clairac G
Biferi MG
Berthault C
Serraf A
Nottin R
Klatzmann D
Cumano A
Barkats M
Le Panse R
Berrih-Aknin S
Source :
The Journal of clinical investigation [J Clin Invest] 2016 Apr 01; Vol. 126 (4), pp. 1525-37. Date of Electronic Publication: 2016 Mar 21.
Publication Year :
2016

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.

Details

Language :
English
ISSN :
1558-8238
Volume :
126
Issue :
4
Database :
MEDLINE
Journal :
The Journal of clinical investigation
Publication Type :
Academic Journal
Accession number :
26999605
Full Text :
https://doi.org/10.1172/JCI81894