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Preclinical modeling of myelodysplastic syndromes
Myelodysplastic syndromes (MDS) represent a heterogeneous group of hematological clonal disorders. Here, we have tested the bone marrow (BM) cells from 38 MDS patients covering all risk groups in two immunodeficient mouse models: NSG and NSG-S. Our data show comparable level of engraftment in both m...
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/PMC5729336/ https://www.ncbi.nlm.nih.gov/pubmed/28663577 http://dx.doi.org/10.1038/leu.2017.172 |
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author | Rouault-Pierre, K Mian, S A Goulard, M Abarrategi, A Di Tulio, A Smith, A E Mohamedali, A Best, S Nloga, A-M Kulasekararaj, A G Ades, L Chomienne, C Fenaux, P Dosquet, C Mufti, G J Bonnet, D |
author_facet | Rouault-Pierre, K Mian, S A Goulard, M Abarrategi, A Di Tulio, A Smith, A E Mohamedali, A Best, S Nloga, A-M Kulasekararaj, A G Ades, L Chomienne, C Fenaux, P Dosquet, C Mufti, G J Bonnet, D |
author_sort | Rouault-Pierre, K |
collection | PubMed |
description | Myelodysplastic syndromes (MDS) represent a heterogeneous group of hematological clonal disorders. Here, we have tested the bone marrow (BM) cells from 38 MDS patients covering all risk groups in two immunodeficient mouse models: NSG and NSG-S. Our data show comparable level of engraftment in both models. The level of engraftment was patient specific with no correlation to any specific MDS risk group. Furthermore, the co-injection of mesenchymal stromal cells (MSCs) did not improve the level of engraftment. Finally, we have developed an in vitro two-dimensional co-culture system as an alternative tool to in vivo. Using our in vitro system, we have been able to co-culture CD34(+) cells from MDS patient BM on auto- and/or allogeneic MSCs over 4 weeks with a fold expansion of up to 600 times. More importantly, these expanded cells conserved their MDS clonal architecture as well as genomic integrity. |
format | Online Article Text |
id | pubmed-5729336 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-57293362017-12-15 Preclinical modeling of myelodysplastic syndromes Rouault-Pierre, K Mian, S A Goulard, M Abarrategi, A Di Tulio, A Smith, A E Mohamedali, A Best, S Nloga, A-M Kulasekararaj, A G Ades, L Chomienne, C Fenaux, P Dosquet, C Mufti, G J Bonnet, D Leukemia Original Article Myelodysplastic syndromes (MDS) represent a heterogeneous group of hematological clonal disorders. Here, we have tested the bone marrow (BM) cells from 38 MDS patients covering all risk groups in two immunodeficient mouse models: NSG and NSG-S. Our data show comparable level of engraftment in both models. The level of engraftment was patient specific with no correlation to any specific MDS risk group. Furthermore, the co-injection of mesenchymal stromal cells (MSCs) did not improve the level of engraftment. Finally, we have developed an in vitro two-dimensional co-culture system as an alternative tool to in vivo. Using our in vitro system, we have been able to co-culture CD34(+) cells from MDS patient BM on auto- and/or allogeneic MSCs over 4 weeks with a fold expansion of up to 600 times. More importantly, these expanded cells conserved their MDS clonal architecture as well as genomic integrity. Nature Publishing Group 2017-12 2017-06-30 /pmc/articles/PMC5729336/ /pubmed/28663577 http://dx.doi.org/10.1038/leu.2017.172 Text en Copyright © 2017 The Author(s) 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 | Original Article Rouault-Pierre, K Mian, S A Goulard, M Abarrategi, A Di Tulio, A Smith, A E Mohamedali, A Best, S Nloga, A-M Kulasekararaj, A G Ades, L Chomienne, C Fenaux, P Dosquet, C Mufti, G J Bonnet, D Preclinical modeling of myelodysplastic syndromes |
title | Preclinical modeling of myelodysplastic syndromes |
title_full | Preclinical modeling of myelodysplastic syndromes |
title_fullStr | Preclinical modeling of myelodysplastic syndromes |
title_full_unstemmed | Preclinical modeling of myelodysplastic syndromes |
title_short | Preclinical modeling of myelodysplastic syndromes |
title_sort | preclinical modeling of myelodysplastic syndromes |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5729336/ https://www.ncbi.nlm.nih.gov/pubmed/28663577 http://dx.doi.org/10.1038/leu.2017.172 |
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