Cargando…
Regulatory T cells inhibit CD34+ cell differentiation into NK cells by blocking their proliferation
Graft versus Host Disease (GvHD) remains one of the main complications after hematopoietic stem cell transplantation (HSCT). Due to their ability to suppress effector cells, regulatory T cells (Tregs) have been proposed as a cellular therapy to prevent GvHD, however they also inhibit the functions o...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4768165/ https://www.ncbi.nlm.nih.gov/pubmed/26915707 http://dx.doi.org/10.1038/srep22097 |
_version_ | 1782417904384344064 |
---|---|
author | Pedroza-Pacheco, Isabela Shah, Divya Domogala, Anna Luevano, Martha Blundell, Michael Jackson, Nicola Thrasher, Adrian Madrigal, Alejandro Saudemont, Aurore |
author_facet | Pedroza-Pacheco, Isabela Shah, Divya Domogala, Anna Luevano, Martha Blundell, Michael Jackson, Nicola Thrasher, Adrian Madrigal, Alejandro Saudemont, Aurore |
author_sort | Pedroza-Pacheco, Isabela |
collection | PubMed |
description | Graft versus Host Disease (GvHD) remains one of the main complications after hematopoietic stem cell transplantation (HSCT). Due to their ability to suppress effector cells, regulatory T cells (Tregs) have been proposed as a cellular therapy to prevent GvHD, however they also inhibit the functions of natural killer (NK) cells, key effectors of the Graft versus Leukemia effect. In this study, we have explored whether a Tregs therapy will also impact on NK cell differentiation. Using an in vitro model of hematopoietic stem cell (HSC) differentiation into NK cells, we found that activated Tregs led to a 90% reduction in NK cell numbers when added at the time of commitment to the NK cell lineage. This effect was contact dependent and was reversible upon Tregs depletion. The few NK cells that developed in these cultures were mature and exhibited normal functions. Furthermore, adoptive transfer of activated Tregs in rag(-/-) γc(-/-) mice abrogated HSC differentiation into NK cells thus confirming our in vitro findings. Collectively, these results demonstrate for the first time that activated Tregs can inhibit NK cell differentiation from HSC under specific conditions. |
format | Online Article Text |
id | pubmed-4768165 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47681652016-03-02 Regulatory T cells inhibit CD34+ cell differentiation into NK cells by blocking their proliferation Pedroza-Pacheco, Isabela Shah, Divya Domogala, Anna Luevano, Martha Blundell, Michael Jackson, Nicola Thrasher, Adrian Madrigal, Alejandro Saudemont, Aurore Sci Rep Article Graft versus Host Disease (GvHD) remains one of the main complications after hematopoietic stem cell transplantation (HSCT). Due to their ability to suppress effector cells, regulatory T cells (Tregs) have been proposed as a cellular therapy to prevent GvHD, however they also inhibit the functions of natural killer (NK) cells, key effectors of the Graft versus Leukemia effect. In this study, we have explored whether a Tregs therapy will also impact on NK cell differentiation. Using an in vitro model of hematopoietic stem cell (HSC) differentiation into NK cells, we found that activated Tregs led to a 90% reduction in NK cell numbers when added at the time of commitment to the NK cell lineage. This effect was contact dependent and was reversible upon Tregs depletion. The few NK cells that developed in these cultures were mature and exhibited normal functions. Furthermore, adoptive transfer of activated Tregs in rag(-/-) γc(-/-) mice abrogated HSC differentiation into NK cells thus confirming our in vitro findings. Collectively, these results demonstrate for the first time that activated Tregs can inhibit NK cell differentiation from HSC under specific conditions. Nature Publishing Group 2016-02-26 /pmc/articles/PMC4768165/ /pubmed/26915707 http://dx.doi.org/10.1038/srep22097 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Pedroza-Pacheco, Isabela Shah, Divya Domogala, Anna Luevano, Martha Blundell, Michael Jackson, Nicola Thrasher, Adrian Madrigal, Alejandro Saudemont, Aurore Regulatory T cells inhibit CD34+ cell differentiation into NK cells by blocking their proliferation |
title | Regulatory T cells inhibit CD34+ cell differentiation into NK cells by blocking their proliferation |
title_full | Regulatory T cells inhibit CD34+ cell differentiation into NK cells by blocking their proliferation |
title_fullStr | Regulatory T cells inhibit CD34+ cell differentiation into NK cells by blocking their proliferation |
title_full_unstemmed | Regulatory T cells inhibit CD34+ cell differentiation into NK cells by blocking their proliferation |
title_short | Regulatory T cells inhibit CD34+ cell differentiation into NK cells by blocking their proliferation |
title_sort | regulatory t cells inhibit cd34+ cell differentiation into nk cells by blocking their proliferation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4768165/ https://www.ncbi.nlm.nih.gov/pubmed/26915707 http://dx.doi.org/10.1038/srep22097 |
work_keys_str_mv | AT pedrozapachecoisabela regulatorytcellsinhibitcd34celldifferentiationintonkcellsbyblockingtheirproliferation AT shahdivya regulatorytcellsinhibitcd34celldifferentiationintonkcellsbyblockingtheirproliferation AT domogalaanna regulatorytcellsinhibitcd34celldifferentiationintonkcellsbyblockingtheirproliferation AT luevanomartha regulatorytcellsinhibitcd34celldifferentiationintonkcellsbyblockingtheirproliferation AT blundellmichael regulatorytcellsinhibitcd34celldifferentiationintonkcellsbyblockingtheirproliferation AT jacksonnicola regulatorytcellsinhibitcd34celldifferentiationintonkcellsbyblockingtheirproliferation AT thrasheradrian regulatorytcellsinhibitcd34celldifferentiationintonkcellsbyblockingtheirproliferation AT madrigalalejandro regulatorytcellsinhibitcd34celldifferentiationintonkcellsbyblockingtheirproliferation AT saudemontaurore regulatorytcellsinhibitcd34celldifferentiationintonkcellsbyblockingtheirproliferation |