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Lkb1 maintains T(reg) cell lineage identity
Regulatory T (T(reg)) cells are a distinct T-cell lineage characterized by sustained Foxp3 expression and potent suppressor function, but the upstream dominant factors that preserve T(reg) lineage-specific features are mostly unknown. Here, we show that Lkb1 maintains T(reg) cell lineage identity by...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5481770/ https://www.ncbi.nlm.nih.gov/pubmed/28621313 http://dx.doi.org/10.1038/ncomms15876 |
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author | Wu, Di Luo, Yuechen Guo, Wei Niu, Qing Xue, Ting Yang, Fei Sun, Xiaolei Chen, Song Liu, Yuanyuan Liu, Jingru Sun, Zhina Zhao, Chunxiao Huang, Huifang Liao, Fang Han, Zhongchao Zhou, Dongming Yang, Yongguang Xu, Guogang Cheng, Tao Feng, Xiaoming |
author_facet | Wu, Di Luo, Yuechen Guo, Wei Niu, Qing Xue, Ting Yang, Fei Sun, Xiaolei Chen, Song Liu, Yuanyuan Liu, Jingru Sun, Zhina Zhao, Chunxiao Huang, Huifang Liao, Fang Han, Zhongchao Zhou, Dongming Yang, Yongguang Xu, Guogang Cheng, Tao Feng, Xiaoming |
author_sort | Wu, Di |
collection | PubMed |
description | Regulatory T (T(reg)) cells are a distinct T-cell lineage characterized by sustained Foxp3 expression and potent suppressor function, but the upstream dominant factors that preserve T(reg) lineage-specific features are mostly unknown. Here, we show that Lkb1 maintains T(reg) cell lineage identity by stabilizing Foxp3 expression and enforcing suppressor function. Upon T-cell receptor (TCR) stimulation Lkb1 protein expression is upregulated in T(reg) cells but not in conventional T cells. Mice with T(reg) cell-specific deletion of Lkb1 develop a fatal early-onset autoimmune disease, with no Foxp3 expression in most T(reg) cells. Lkb1 stabilizes Foxp3 expression by preventing STAT4-mediated methylation of the conserved noncoding sequence 2 (CNS2) in the Foxp3 locus. Independent of maintaining Foxp3 expression, Lkb1 programs the expression of a wide spectrum of immunosuppressive genes, through mechanisms involving the augmentation of TGF-β signalling. These findings identify a critical function of Lkb1 in maintaining T(reg) cell lineage identity. |
format | Online Article Text |
id | pubmed-5481770 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-54817702017-07-06 Lkb1 maintains T(reg) cell lineage identity Wu, Di Luo, Yuechen Guo, Wei Niu, Qing Xue, Ting Yang, Fei Sun, Xiaolei Chen, Song Liu, Yuanyuan Liu, Jingru Sun, Zhina Zhao, Chunxiao Huang, Huifang Liao, Fang Han, Zhongchao Zhou, Dongming Yang, Yongguang Xu, Guogang Cheng, Tao Feng, Xiaoming Nat Commun Article Regulatory T (T(reg)) cells are a distinct T-cell lineage characterized by sustained Foxp3 expression and potent suppressor function, but the upstream dominant factors that preserve T(reg) lineage-specific features are mostly unknown. Here, we show that Lkb1 maintains T(reg) cell lineage identity by stabilizing Foxp3 expression and enforcing suppressor function. Upon T-cell receptor (TCR) stimulation Lkb1 protein expression is upregulated in T(reg) cells but not in conventional T cells. Mice with T(reg) cell-specific deletion of Lkb1 develop a fatal early-onset autoimmune disease, with no Foxp3 expression in most T(reg) cells. Lkb1 stabilizes Foxp3 expression by preventing STAT4-mediated methylation of the conserved noncoding sequence 2 (CNS2) in the Foxp3 locus. Independent of maintaining Foxp3 expression, Lkb1 programs the expression of a wide spectrum of immunosuppressive genes, through mechanisms involving the augmentation of TGF-β signalling. These findings identify a critical function of Lkb1 in maintaining T(reg) cell lineage identity. Nature Publishing Group 2017-06-16 /pmc/articles/PMC5481770/ /pubmed/28621313 http://dx.doi.org/10.1038/ncomms15876 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Wu, Di Luo, Yuechen Guo, Wei Niu, Qing Xue, Ting Yang, Fei Sun, Xiaolei Chen, Song Liu, Yuanyuan Liu, Jingru Sun, Zhina Zhao, Chunxiao Huang, Huifang Liao, Fang Han, Zhongchao Zhou, Dongming Yang, Yongguang Xu, Guogang Cheng, Tao Feng, Xiaoming Lkb1 maintains T(reg) cell lineage identity |
title | Lkb1 maintains T(reg) cell lineage identity |
title_full | Lkb1 maintains T(reg) cell lineage identity |
title_fullStr | Lkb1 maintains T(reg) cell lineage identity |
title_full_unstemmed | Lkb1 maintains T(reg) cell lineage identity |
title_short | Lkb1 maintains T(reg) cell lineage identity |
title_sort | lkb1 maintains t(reg) cell lineage identity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5481770/ https://www.ncbi.nlm.nih.gov/pubmed/28621313 http://dx.doi.org/10.1038/ncomms15876 |
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