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NFAT2 is a critical regulator of the anergic phenotype in chronic lymphocytic leukaemia
Chronic lymphocytic leukaemia (CLL) is a clonal disorder of mature B cells. Most patients are characterised by an indolent disease course and an anergic phenotype of their leukaemia cells, which refers to a state of unresponsiveness to B cell receptor stimulation. Up to 10% of CLL patients transform...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5624906/ https://www.ncbi.nlm.nih.gov/pubmed/28970470 http://dx.doi.org/10.1038/s41467-017-00830-y |
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author | Märklin, Melanie Heitmann, Jonas S. Fuchs, Alexander R. Truckenmüller, Felicia M. Gutknecht, Michael Bugl, Stefanie Saur, Sebastian J. Lazarus, Juliane Kohlhofer, Ursula Quintanilla-Martinez, Leticia Rammensee, Hans-Georg Salih, Helmut R. Kopp, Hans-Georg Haap, Michael Kirschniak, Andreas Kanz, Lothar Rao, Anjana Wirths, Stefan Müller, Martin R. |
author_facet | Märklin, Melanie Heitmann, Jonas S. Fuchs, Alexander R. Truckenmüller, Felicia M. Gutknecht, Michael Bugl, Stefanie Saur, Sebastian J. Lazarus, Juliane Kohlhofer, Ursula Quintanilla-Martinez, Leticia Rammensee, Hans-Georg Salih, Helmut R. Kopp, Hans-Georg Haap, Michael Kirschniak, Andreas Kanz, Lothar Rao, Anjana Wirths, Stefan Müller, Martin R. |
author_sort | Märklin, Melanie |
collection | PubMed |
description | Chronic lymphocytic leukaemia (CLL) is a clonal disorder of mature B cells. Most patients are characterised by an indolent disease course and an anergic phenotype of their leukaemia cells, which refers to a state of unresponsiveness to B cell receptor stimulation. Up to 10% of CLL patients transform from an indolent subtype to an aggressive form of B cell lymphoma over time (Richter´s syndrome) and show a significantly worse treatment outcome. Here we show that B cell-specific ablation of Nfat2 leads to the loss of the anergic phenotype culminating in a significantly compromised life expectancy and transformation to aggressive disease. We further define a gene expression signature of anergic CLL cells consisting of several NFAT2-dependent genes including Cbl-b, Grail, Egr2 and Lck. In summary, this study identifies NFAT2 as a crucial regulator of the anergic phenotype in CLL. |
format | Online Article Text |
id | pubmed-5624906 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56249062017-10-04 NFAT2 is a critical regulator of the anergic phenotype in chronic lymphocytic leukaemia Märklin, Melanie Heitmann, Jonas S. Fuchs, Alexander R. Truckenmüller, Felicia M. Gutknecht, Michael Bugl, Stefanie Saur, Sebastian J. Lazarus, Juliane Kohlhofer, Ursula Quintanilla-Martinez, Leticia Rammensee, Hans-Georg Salih, Helmut R. Kopp, Hans-Georg Haap, Michael Kirschniak, Andreas Kanz, Lothar Rao, Anjana Wirths, Stefan Müller, Martin R. Nat Commun Article Chronic lymphocytic leukaemia (CLL) is a clonal disorder of mature B cells. Most patients are characterised by an indolent disease course and an anergic phenotype of their leukaemia cells, which refers to a state of unresponsiveness to B cell receptor stimulation. Up to 10% of CLL patients transform from an indolent subtype to an aggressive form of B cell lymphoma over time (Richter´s syndrome) and show a significantly worse treatment outcome. Here we show that B cell-specific ablation of Nfat2 leads to the loss of the anergic phenotype culminating in a significantly compromised life expectancy and transformation to aggressive disease. We further define a gene expression signature of anergic CLL cells consisting of several NFAT2-dependent genes including Cbl-b, Grail, Egr2 and Lck. In summary, this study identifies NFAT2 as a crucial regulator of the anergic phenotype in CLL. Nature Publishing Group UK 2017-10-02 /pmc/articles/PMC5624906/ /pubmed/28970470 http://dx.doi.org/10.1038/s41467-017-00830-y Text en © The Author(s) 2017 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 Märklin, Melanie Heitmann, Jonas S. Fuchs, Alexander R. Truckenmüller, Felicia M. Gutknecht, Michael Bugl, Stefanie Saur, Sebastian J. Lazarus, Juliane Kohlhofer, Ursula Quintanilla-Martinez, Leticia Rammensee, Hans-Georg Salih, Helmut R. Kopp, Hans-Georg Haap, Michael Kirschniak, Andreas Kanz, Lothar Rao, Anjana Wirths, Stefan Müller, Martin R. NFAT2 is a critical regulator of the anergic phenotype in chronic lymphocytic leukaemia |
title | NFAT2 is a critical regulator of the anergic phenotype in chronic lymphocytic leukaemia |
title_full | NFAT2 is a critical regulator of the anergic phenotype in chronic lymphocytic leukaemia |
title_fullStr | NFAT2 is a critical regulator of the anergic phenotype in chronic lymphocytic leukaemia |
title_full_unstemmed | NFAT2 is a critical regulator of the anergic phenotype in chronic lymphocytic leukaemia |
title_short | NFAT2 is a critical regulator of the anergic phenotype in chronic lymphocytic leukaemia |
title_sort | nfat2 is a critical regulator of the anergic phenotype in chronic lymphocytic leukaemia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5624906/ https://www.ncbi.nlm.nih.gov/pubmed/28970470 http://dx.doi.org/10.1038/s41467-017-00830-y |
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