Cargando…
Aire and Fezf2, two regulators in medullary thymic epithelial cells, control autoimmune diseases by regulating TSAs: Partner or complementer?
The expression of tissue-specific antigens (TSAs) in medullary thymic epithelial cells (mTECs) is believed to be responsible for the elimination of autoreactive T cells, a critical process in the maintenance of central immune tolerance. The transcription factor autoimmune regulator (Aire) and FEZ fa...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9468217/ https://www.ncbi.nlm.nih.gov/pubmed/36110862 http://dx.doi.org/10.3389/fimmu.2022.948259 |
_version_ | 1784788361238544384 |
---|---|
author | Qi, Yanfei Zhang, Rongchao Lu, Yaoping Zou, Xueyang Yang, Wei |
author_facet | Qi, Yanfei Zhang, Rongchao Lu, Yaoping Zou, Xueyang Yang, Wei |
author_sort | Qi, Yanfei |
collection | PubMed |
description | The expression of tissue-specific antigens (TSAs) in medullary thymic epithelial cells (mTECs) is believed to be responsible for the elimination of autoreactive T cells, a critical process in the maintenance of central immune tolerance. The transcription factor autoimmune regulator (Aire) and FEZ family zinc finger 2(Fezf2) play an essential role in driving the expression of TSAs in mTECs, while their deficiency in humans and mice causes a range of autoimmune manifestations, such as type 1 diabetes, Sjögren’s syndrome and rheumatoid arthritis. However, because of their regulatory mechanisms, the expression profile of TSAs and their relationship with special autoimmune diseases are still in dispute. In this review, we compare the roles of Aire and Fezf2 in regulating TSAs, with an emphasis on their molecular mechanisms in autoimmune diseases, which provides the foundation for devising improved diagnostic and therapeutic approaches for patients. |
format | Online Article Text |
id | pubmed-9468217 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-94682172022-09-14 Aire and Fezf2, two regulators in medullary thymic epithelial cells, control autoimmune diseases by regulating TSAs: Partner or complementer? Qi, Yanfei Zhang, Rongchao Lu, Yaoping Zou, Xueyang Yang, Wei Front Immunol Immunology The expression of tissue-specific antigens (TSAs) in medullary thymic epithelial cells (mTECs) is believed to be responsible for the elimination of autoreactive T cells, a critical process in the maintenance of central immune tolerance. The transcription factor autoimmune regulator (Aire) and FEZ family zinc finger 2(Fezf2) play an essential role in driving the expression of TSAs in mTECs, while their deficiency in humans and mice causes a range of autoimmune manifestations, such as type 1 diabetes, Sjögren’s syndrome and rheumatoid arthritis. However, because of their regulatory mechanisms, the expression profile of TSAs and their relationship with special autoimmune diseases are still in dispute. In this review, we compare the roles of Aire and Fezf2 in regulating TSAs, with an emphasis on their molecular mechanisms in autoimmune diseases, which provides the foundation for devising improved diagnostic and therapeutic approaches for patients. Frontiers Media S.A. 2022-08-30 /pmc/articles/PMC9468217/ /pubmed/36110862 http://dx.doi.org/10.3389/fimmu.2022.948259 Text en Copyright © 2022 Qi, Zhang, Lu, Zou and Yang https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Qi, Yanfei Zhang, Rongchao Lu, Yaoping Zou, Xueyang Yang, Wei Aire and Fezf2, two regulators in medullary thymic epithelial cells, control autoimmune diseases by regulating TSAs: Partner or complementer? |
title | Aire and Fezf2, two regulators in medullary thymic epithelial cells, control autoimmune diseases by regulating TSAs: Partner or complementer? |
title_full | Aire and Fezf2, two regulators in medullary thymic epithelial cells, control autoimmune diseases by regulating TSAs: Partner or complementer? |
title_fullStr | Aire and Fezf2, two regulators in medullary thymic epithelial cells, control autoimmune diseases by regulating TSAs: Partner or complementer? |
title_full_unstemmed | Aire and Fezf2, two regulators in medullary thymic epithelial cells, control autoimmune diseases by regulating TSAs: Partner or complementer? |
title_short | Aire and Fezf2, two regulators in medullary thymic epithelial cells, control autoimmune diseases by regulating TSAs: Partner or complementer? |
title_sort | aire and fezf2, two regulators in medullary thymic epithelial cells, control autoimmune diseases by regulating tsas: partner or complementer? |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9468217/ https://www.ncbi.nlm.nih.gov/pubmed/36110862 http://dx.doi.org/10.3389/fimmu.2022.948259 |
work_keys_str_mv | AT qiyanfei aireandfezf2tworegulatorsinmedullarythymicepithelialcellscontrolautoimmunediseasesbyregulatingtsaspartnerorcomplementer AT zhangrongchao aireandfezf2tworegulatorsinmedullarythymicepithelialcellscontrolautoimmunediseasesbyregulatingtsaspartnerorcomplementer AT luyaoping aireandfezf2tworegulatorsinmedullarythymicepithelialcellscontrolautoimmunediseasesbyregulatingtsaspartnerorcomplementer AT zouxueyang aireandfezf2tworegulatorsinmedullarythymicepithelialcellscontrolautoimmunediseasesbyregulatingtsaspartnerorcomplementer AT yangwei aireandfezf2tworegulatorsinmedullarythymicepithelialcellscontrolautoimmunediseasesbyregulatingtsaspartnerorcomplementer |