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Link between the EZH2 noncanonical pathway and microtubule organization center polarization during early T lymphopoiesis
EZH2 plays an essential role at the β-selection checkpoint of T lymphopoiesis by regulating histone H3 lysine 27 trimethylation (H3K27me3) via its canonical mode of action. Increasing data suggest that EZH2 could also regulate other cellular functions, such as cytoskeletal reorganization, via its no...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8901749/ https://www.ncbi.nlm.nih.gov/pubmed/35256668 http://dx.doi.org/10.1038/s41598-022-07684-5 |
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author | Deshayes, Frederique Fradet, Magali Kaminski, Sandra Viguier, Mireille Frippiat, Jean-Pol Ghislin, Stephanie |
author_facet | Deshayes, Frederique Fradet, Magali Kaminski, Sandra Viguier, Mireille Frippiat, Jean-Pol Ghislin, Stephanie |
author_sort | Deshayes, Frederique |
collection | PubMed |
description | EZH2 plays an essential role at the β-selection checkpoint of T lymphopoiesis by regulating histone H3 lysine 27 trimethylation (H3K27me3) via its canonical mode of action. Increasing data suggest that EZH2 could also regulate other cellular functions, such as cytoskeletal reorganization, via its noncanonical pathway. Consequently, we investigated whether the EZH2 noncanonical pathway could be involved in early T-cell maturation, which requires cell polarization. We observed that EZH2 localization is tightly regulated during the early stages of T-cell development and that EZH2 relocalizes in the nucleus of double-negative thymocytes enduring TCRβ recombination and β-selection processes. Furthermore, we observed that EZH2 and EED, but not Suz12, colocalize with the microtubule organization center (MTOC), which might prevent its inappropriate polarization in double negative cells. In accordance with these results, we evidenced the existence of direct or indirect interaction between EED and α-tubulin. Taken together, these results suggest that the EZH2 noncanonical pathway, in association with EED, is involved in the early stages of T-cell maturation. |
format | Online Article Text |
id | pubmed-8901749 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-89017492022-03-08 Link between the EZH2 noncanonical pathway and microtubule organization center polarization during early T lymphopoiesis Deshayes, Frederique Fradet, Magali Kaminski, Sandra Viguier, Mireille Frippiat, Jean-Pol Ghislin, Stephanie Sci Rep Article EZH2 plays an essential role at the β-selection checkpoint of T lymphopoiesis by regulating histone H3 lysine 27 trimethylation (H3K27me3) via its canonical mode of action. Increasing data suggest that EZH2 could also regulate other cellular functions, such as cytoskeletal reorganization, via its noncanonical pathway. Consequently, we investigated whether the EZH2 noncanonical pathway could be involved in early T-cell maturation, which requires cell polarization. We observed that EZH2 localization is tightly regulated during the early stages of T-cell development and that EZH2 relocalizes in the nucleus of double-negative thymocytes enduring TCRβ recombination and β-selection processes. Furthermore, we observed that EZH2 and EED, but not Suz12, colocalize with the microtubule organization center (MTOC), which might prevent its inappropriate polarization in double negative cells. In accordance with these results, we evidenced the existence of direct or indirect interaction between EED and α-tubulin. Taken together, these results suggest that the EZH2 noncanonical pathway, in association with EED, is involved in the early stages of T-cell maturation. Nature Publishing Group UK 2022-03-07 /pmc/articles/PMC8901749/ /pubmed/35256668 http://dx.doi.org/10.1038/s41598-022-07684-5 Text en © The Author(s) 2022 https://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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Deshayes, Frederique Fradet, Magali Kaminski, Sandra Viguier, Mireille Frippiat, Jean-Pol Ghislin, Stephanie Link between the EZH2 noncanonical pathway and microtubule organization center polarization during early T lymphopoiesis |
title | Link between the EZH2 noncanonical pathway and microtubule organization center polarization during early T lymphopoiesis |
title_full | Link between the EZH2 noncanonical pathway and microtubule organization center polarization during early T lymphopoiesis |
title_fullStr | Link between the EZH2 noncanonical pathway and microtubule organization center polarization during early T lymphopoiesis |
title_full_unstemmed | Link between the EZH2 noncanonical pathway and microtubule organization center polarization during early T lymphopoiesis |
title_short | Link between the EZH2 noncanonical pathway and microtubule organization center polarization during early T lymphopoiesis |
title_sort | link between the ezh2 noncanonical pathway and microtubule organization center polarization during early t lymphopoiesis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8901749/ https://www.ncbi.nlm.nih.gov/pubmed/35256668 http://dx.doi.org/10.1038/s41598-022-07684-5 |
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