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DGCR8-Mediated Production of Canonical Micrornas Is Critical for Regulatory T Cell Function and Stability
Regulatory T cells (Treg) are integral for immune homeostasis. Here we demonstrate that canonical microRNAs (miRNAs) are required for Treg function because mice with DGCR8-deficient Treg cells spontaneously develop a scurfy-like disease. Using genetic lineage marking we show that absence of miRNAs l...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3669207/ https://www.ncbi.nlm.nih.gov/pubmed/23741528 http://dx.doi.org/10.1371/journal.pone.0066282 |
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author | Jeker, Lukas T. Zhou, Xuyu Blelloch, Robert Bluestone, Jeffrey A. |
author_facet | Jeker, Lukas T. Zhou, Xuyu Blelloch, Robert Bluestone, Jeffrey A. |
author_sort | Jeker, Lukas T. |
collection | PubMed |
description | Regulatory T cells (Treg) are integral for immune homeostasis. Here we demonstrate that canonical microRNAs (miRNAs) are required for Treg function because mice with DGCR8-deficient Treg cells spontaneously develop a scurfy-like disease. Using genetic lineage marking we show that absence of miRNAs leads to reduced FoxP3 expression in Treg cells in vivo. In vitro culture of purified DGCR8-deficient Treg leads to a loss of FoxP3 expression. We conclude that canonical miRNAs are essential to maintain stable FoxP3 expression and Treg function. Thus, signals interfering with miRNA homeostasis might contribute to autoimmune diseases. |
format | Online Article Text |
id | pubmed-3669207 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-36692072013-06-05 DGCR8-Mediated Production of Canonical Micrornas Is Critical for Regulatory T Cell Function and Stability Jeker, Lukas T. Zhou, Xuyu Blelloch, Robert Bluestone, Jeffrey A. PLoS One Research Article Regulatory T cells (Treg) are integral for immune homeostasis. Here we demonstrate that canonical microRNAs (miRNAs) are required for Treg function because mice with DGCR8-deficient Treg cells spontaneously develop a scurfy-like disease. Using genetic lineage marking we show that absence of miRNAs leads to reduced FoxP3 expression in Treg cells in vivo. In vitro culture of purified DGCR8-deficient Treg leads to a loss of FoxP3 expression. We conclude that canonical miRNAs are essential to maintain stable FoxP3 expression and Treg function. Thus, signals interfering with miRNA homeostasis might contribute to autoimmune diseases. Public Library of Science 2013-05-31 /pmc/articles/PMC3669207/ /pubmed/23741528 http://dx.doi.org/10.1371/journal.pone.0066282 Text en © 2013 Jeker et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Jeker, Lukas T. Zhou, Xuyu Blelloch, Robert Bluestone, Jeffrey A. DGCR8-Mediated Production of Canonical Micrornas Is Critical for Regulatory T Cell Function and Stability |
title | DGCR8-Mediated Production of Canonical Micrornas Is Critical for Regulatory T Cell Function and Stability |
title_full | DGCR8-Mediated Production of Canonical Micrornas Is Critical for Regulatory T Cell Function and Stability |
title_fullStr | DGCR8-Mediated Production of Canonical Micrornas Is Critical for Regulatory T Cell Function and Stability |
title_full_unstemmed | DGCR8-Mediated Production of Canonical Micrornas Is Critical for Regulatory T Cell Function and Stability |
title_short | DGCR8-Mediated Production of Canonical Micrornas Is Critical for Regulatory T Cell Function and Stability |
title_sort | dgcr8-mediated production of canonical micrornas is critical for regulatory t cell function and stability |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3669207/ https://www.ncbi.nlm.nih.gov/pubmed/23741528 http://dx.doi.org/10.1371/journal.pone.0066282 |
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