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

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  • معلومة اضافية
    • Contributors:
      Centre de recherche en myologie; Université Pierre et Marie Curie - Paris 6 (UPMC)-Association française contre les myopathies (AFM-Téléthon)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS); Remodelage tissulaire et fonctionnel : signalisation et physio-pathologie (RTFSPP); Université Paris-Sud - Paris 11 (UP11)-Centre Chirurgical Marie Lannelongue (CCML)-Centre National de la Recherche Scientifique (CNRS); Cellule Pasteur; Université Paris Diderot - Paris 7 (UPD7)-PRES Sorbonne Paris Cité; Lymphopoïèse; Institut Pasteur Paris (IP)-Institut National de la Santé et de la Recherche Médicale (INSERM); Centre Chirurgical Marie Lannelongue (CCML); Immunologie - Immunopathologie - Immunothérapie (I3); Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS); Institut de Myologie; Université Pierre et Marie Curie - Paris 6 (UPMC)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Association française contre les myopathies (AFM-Téléthon)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS); This work was supported by MYASTAID (LSHM-CT-2006-037833) and FIGHT-MG (HEALTH-2009-242-210) grants from the European Community and a grant from the Association Française contre les Myopathies obtained by S. Berrih-Aknin.; European Project: 38962,MYASTAID; European Project: 242210,EC:FP7:HEALTH,FP7-HEALTH-2009-single-stage,FIGHT-MG(2009)
    • بيانات النشر:
      HAL CCSD
      American Society for Clinical Investigation
    • الموضوع:
      2016
    • Collection:
      Institut Pasteur: HAL
    • نبذة مختصرة :
      International audience ; 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.
    • Relation:
      info:eu-repo/semantics/altIdentifier/pmid/26999605; info:eu-repo/grantAgreement//38962/EU/Development of models to improve management of Myasthenia Gravis: From basic knowledge to clinical application/MYASTAID; info:eu-repo/grantAgreement/EC/FP7/242210/EU/Myasthenias, a group of immune mediated neurological diseases: from etiology to therapy./FIGHT-MG; hal-01310502; https://hal.sorbonne-universite.fr/hal-01310502; https://hal.sorbonne-universite.fr/hal-01310502/document; https://hal.sorbonne-universite.fr/hal-01310502/file/JCI81894.pdf; PUBMED: 26999605; PUBMEDCENTRAL: PMC4811157
    • الرقم المعرف:
      10.1172/JCI81894
    • Rights:
      http://creativecommons.org/licenses/by/ ; info:eu-repo/semantics/OpenAccess
    • الرقم المعرف:
      edsbas.4666B5E6