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Biphasic Aire expression in early embryos and in medullary thymic epithelial cells before end-stage terminal differentiation
The roles of autoimmune regulator (Aire)–expressing medullary thymic epithelial cells (mTECs) in the organization of the thymic microenvironment for establishing self-tolerance are enigmatic. We sought to monitor the production and maintenance of Aire-expressing mTECs by a fate-mapping strategy in w...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2867289/ https://www.ncbi.nlm.nih.gov/pubmed/20404099 http://dx.doi.org/10.1084/jem.20092144 |
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author | Nishikawa, Yumiko Hirota, Fumiko Yano, Masashi Kitajima, Hiroyuki Miyazaki, Jun-ichi Kawamoto, Hiroshi Mouri, Yasuhiro Matsumoto, Mitsuru |
author_facet | Nishikawa, Yumiko Hirota, Fumiko Yano, Masashi Kitajima, Hiroyuki Miyazaki, Jun-ichi Kawamoto, Hiroshi Mouri, Yasuhiro Matsumoto, Mitsuru |
author_sort | Nishikawa, Yumiko |
collection | PubMed |
description | The roles of autoimmune regulator (Aire)–expressing medullary thymic epithelial cells (mTECs) in the organization of the thymic microenvironment for establishing self-tolerance are enigmatic. We sought to monitor the production and maintenance of Aire-expressing mTECs by a fate-mapping strategy in which bacterial artificial chromosome transgenic (Tg) mice expressing Cre recombinase under the control of the Aire regulatory element were crossed with a GFP reporter strain. We found that, in addition to its well recognized expression within mature mTECs, Aire was expressed in the early embryo before emergence of the three germ cell layers. This observation may help to explain the development of ectodermal dystrophy often seen in patients with AIRE deficiency. With the use of one Tg line in which Cre recombinase expression was confined to mTECs, we found that Aire(+)CD80(high) mTECs further progressed to an Aire(−)CD80(intermediate) stage, suggesting that Aire expression is not constitutive from after its induction until cell death but instead is down-regulated at the beginning of terminal differentiation. We also demonstrated that many mTECs of Aire-expressing lineage are in close contact with thymic dendritic cells. This close proximity may contribute to transfer of tissue-restricted self-antigens expressed by mTECs to professional antigen-presenting cells. |
format | Text |
id | pubmed-2867289 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-28672892010-11-10 Biphasic Aire expression in early embryos and in medullary thymic epithelial cells before end-stage terminal differentiation Nishikawa, Yumiko Hirota, Fumiko Yano, Masashi Kitajima, Hiroyuki Miyazaki, Jun-ichi Kawamoto, Hiroshi Mouri, Yasuhiro Matsumoto, Mitsuru J Exp Med Brief Definitive Report The roles of autoimmune regulator (Aire)–expressing medullary thymic epithelial cells (mTECs) in the organization of the thymic microenvironment for establishing self-tolerance are enigmatic. We sought to monitor the production and maintenance of Aire-expressing mTECs by a fate-mapping strategy in which bacterial artificial chromosome transgenic (Tg) mice expressing Cre recombinase under the control of the Aire regulatory element were crossed with a GFP reporter strain. We found that, in addition to its well recognized expression within mature mTECs, Aire was expressed in the early embryo before emergence of the three germ cell layers. This observation may help to explain the development of ectodermal dystrophy often seen in patients with AIRE deficiency. With the use of one Tg line in which Cre recombinase expression was confined to mTECs, we found that Aire(+)CD80(high) mTECs further progressed to an Aire(−)CD80(intermediate) stage, suggesting that Aire expression is not constitutive from after its induction until cell death but instead is down-regulated at the beginning of terminal differentiation. We also demonstrated that many mTECs of Aire-expressing lineage are in close contact with thymic dendritic cells. This close proximity may contribute to transfer of tissue-restricted self-antigens expressed by mTECs to professional antigen-presenting cells. The Rockefeller University Press 2010-05-10 /pmc/articles/PMC2867289/ /pubmed/20404099 http://dx.doi.org/10.1084/jem.20092144 Text en © 2010 Nishikawa et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Brief Definitive Report Nishikawa, Yumiko Hirota, Fumiko Yano, Masashi Kitajima, Hiroyuki Miyazaki, Jun-ichi Kawamoto, Hiroshi Mouri, Yasuhiro Matsumoto, Mitsuru Biphasic Aire expression in early embryos and in medullary thymic epithelial cells before end-stage terminal differentiation |
title | Biphasic Aire expression in early embryos and in medullary thymic epithelial cells before end-stage terminal differentiation |
title_full | Biphasic Aire expression in early embryos and in medullary thymic epithelial cells before end-stage terminal differentiation |
title_fullStr | Biphasic Aire expression in early embryos and in medullary thymic epithelial cells before end-stage terminal differentiation |
title_full_unstemmed | Biphasic Aire expression in early embryos and in medullary thymic epithelial cells before end-stage terminal differentiation |
title_short | Biphasic Aire expression in early embryos and in medullary thymic epithelial cells before end-stage terminal differentiation |
title_sort | biphasic aire expression in early embryos and in medullary thymic epithelial cells before end-stage terminal differentiation |
topic | Brief Definitive Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2867289/ https://www.ncbi.nlm.nih.gov/pubmed/20404099 http://dx.doi.org/10.1084/jem.20092144 |
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