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Sex bias in CNS autoimmune disease mediated by androgen control of autoimmune regulator

Male gender is protective against multiple sclerosis and other T-cell-mediated autoimmune diseases. This protection may be due, in part, to higher androgen levels in males. Androgen binds to the androgen receptor (AR) to regulate gene expression, but how androgen protects against autoimmunity is not...

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Autores principales: Zhu, Meng-Lei, Bakhru, Pearl, Conley, Bridget, Nelson, Jennifer S., Free, Meghan, Martin, Aaron, Starmer, Joshua, Wilson, Elizabeth M., Su, Maureen A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5512610/
https://www.ncbi.nlm.nih.gov/pubmed/27072778
http://dx.doi.org/10.1038/ncomms11350
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author Zhu, Meng-Lei
Bakhru, Pearl
Conley, Bridget
Nelson, Jennifer S.
Free, Meghan
Martin, Aaron
Starmer, Joshua
Wilson, Elizabeth M.
Su, Maureen A.
author_facet Zhu, Meng-Lei
Bakhru, Pearl
Conley, Bridget
Nelson, Jennifer S.
Free, Meghan
Martin, Aaron
Starmer, Joshua
Wilson, Elizabeth M.
Su, Maureen A.
author_sort Zhu, Meng-Lei
collection PubMed
description Male gender is protective against multiple sclerosis and other T-cell-mediated autoimmune diseases. This protection may be due, in part, to higher androgen levels in males. Androgen binds to the androgen receptor (AR) to regulate gene expression, but how androgen protects against autoimmunity is not well understood. Autoimmune regulator (Aire) prevents autoimmunity by promoting self-antigen expression in medullary thymic epithelial cells, such that developing T cells that recognize these self-antigens within the thymus undergo clonal deletion. Here we show that androgen upregulates Aire-mediated thymic tolerance to protect against autoimmunity. Androgen recruits AR to Aire promoter regions, with consequent enhancement of Aire transcription. In mice and humans, thymic Aire expression is higher in males compared with females. Androgen administration and male gender protect against autoimmunity in a multiple sclerosis mouse model in an Aire-dependent manner. Thus, androgen control of an intrathymic Aire-mediated tolerance mechanism contributes to gender differences in autoimmunity.
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spelling pubmed-55126102017-07-19 Sex bias in CNS autoimmune disease mediated by androgen control of autoimmune regulator Zhu, Meng-Lei Bakhru, Pearl Conley, Bridget Nelson, Jennifer S. Free, Meghan Martin, Aaron Starmer, Joshua Wilson, Elizabeth M. Su, Maureen A. Nat Commun Article Male gender is protective against multiple sclerosis and other T-cell-mediated autoimmune diseases. This protection may be due, in part, to higher androgen levels in males. Androgen binds to the androgen receptor (AR) to regulate gene expression, but how androgen protects against autoimmunity is not well understood. Autoimmune regulator (Aire) prevents autoimmunity by promoting self-antigen expression in medullary thymic epithelial cells, such that developing T cells that recognize these self-antigens within the thymus undergo clonal deletion. Here we show that androgen upregulates Aire-mediated thymic tolerance to protect against autoimmunity. Androgen recruits AR to Aire promoter regions, with consequent enhancement of Aire transcription. In mice and humans, thymic Aire expression is higher in males compared with females. Androgen administration and male gender protect against autoimmunity in a multiple sclerosis mouse model in an Aire-dependent manner. Thus, androgen control of an intrathymic Aire-mediated tolerance mechanism contributes to gender differences in autoimmunity. Nature Publishing Group 2016-04-13 /pmc/articles/PMC5512610/ /pubmed/27072778 http://dx.doi.org/10.1038/ncomms11350 Text en Copyright © 2016, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Zhu, Meng-Lei
Bakhru, Pearl
Conley, Bridget
Nelson, Jennifer S.
Free, Meghan
Martin, Aaron
Starmer, Joshua
Wilson, Elizabeth M.
Su, Maureen A.
Sex bias in CNS autoimmune disease mediated by androgen control of autoimmune regulator
title Sex bias in CNS autoimmune disease mediated by androgen control of autoimmune regulator
title_full Sex bias in CNS autoimmune disease mediated by androgen control of autoimmune regulator
title_fullStr Sex bias in CNS autoimmune disease mediated by androgen control of autoimmune regulator
title_full_unstemmed Sex bias in CNS autoimmune disease mediated by androgen control of autoimmune regulator
title_short Sex bias in CNS autoimmune disease mediated by androgen control of autoimmune regulator
title_sort sex bias in cns autoimmune disease mediated by androgen control of autoimmune regulator
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5512610/
https://www.ncbi.nlm.nih.gov/pubmed/27072778
http://dx.doi.org/10.1038/ncomms11350
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