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Alternative Splicing of FOXP3—Virtue and Vice
FOXP3 is the lineage-defining transcription factor of CD4+ CD25+ regulatory T cells. While many aspects of its regulation, interaction, and function are conserved among species, alternatively spliced FOXP3 isoforms are expressed only in human cells. This review summarizes current knowledge about alt...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5859138/ https://www.ncbi.nlm.nih.gov/pubmed/29593749 http://dx.doi.org/10.3389/fimmu.2018.00530 |
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author | Mailer, Reiner K. W. |
author_facet | Mailer, Reiner K. W. |
author_sort | Mailer, Reiner K. W. |
collection | PubMed |
description | FOXP3 is the lineage-defining transcription factor of CD4+ CD25+ regulatory T cells. While many aspects of its regulation, interaction, and function are conserved among species, alternatively spliced FOXP3 isoforms are expressed only in human cells. This review summarizes current knowledge about alternative splicing of FOXP3 and the specific functions of FOXP3 isoforms in health and disease. Future perspectives in research and the therapeutic potential of manipulating alternative splicing of FOXP3 are discussed. |
format | Online Article Text |
id | pubmed-5859138 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-58591382018-03-28 Alternative Splicing of FOXP3—Virtue and Vice Mailer, Reiner K. W. Front Immunol Immunology FOXP3 is the lineage-defining transcription factor of CD4+ CD25+ regulatory T cells. While many aspects of its regulation, interaction, and function are conserved among species, alternatively spliced FOXP3 isoforms are expressed only in human cells. This review summarizes current knowledge about alternative splicing of FOXP3 and the specific functions of FOXP3 isoforms in health and disease. Future perspectives in research and the therapeutic potential of manipulating alternative splicing of FOXP3 are discussed. Frontiers Media S.A. 2018-03-13 /pmc/articles/PMC5859138/ /pubmed/29593749 http://dx.doi.org/10.3389/fimmu.2018.00530 Text en Copyright © 2018 Mailer. http://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 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 Mailer, Reiner K. W. Alternative Splicing of FOXP3—Virtue and Vice |
title | Alternative Splicing of FOXP3—Virtue and Vice |
title_full | Alternative Splicing of FOXP3—Virtue and Vice |
title_fullStr | Alternative Splicing of FOXP3—Virtue and Vice |
title_full_unstemmed | Alternative Splicing of FOXP3—Virtue and Vice |
title_short | Alternative Splicing of FOXP3—Virtue and Vice |
title_sort | alternative splicing of foxp3—virtue and vice |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5859138/ https://www.ncbi.nlm.nih.gov/pubmed/29593749 http://dx.doi.org/10.3389/fimmu.2018.00530 |
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