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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.
Affiliation
  • Rouault-Pierre K; Haematopoietic Stem Cell Laboratory, The Francis Crick Institute, London, UK.
  • Mian SA; Haematopoietic Stem Cell Laboratory, The Francis Crick Institute, London, UK.
  • Goulard M; King's College London School of Medicine, Department of Haematological Medicine, London, UK.
  • Abarrategi A; INSERM, UMRS1131-University Paris Diderot, Saint Louis Hospital, Paris, France.
  • Di Tulio A; Haematopoietic Stem Cell Laboratory, The Francis Crick Institute, London, UK.
  • Smith AE; Haematopoietic Stem Cell Laboratory, The Francis Crick Institute, London, UK.
  • Mohamedali A; King's College London School of Medicine, Department of Haematological Medicine, London, UK.
  • Best S; King's College Hospital, Department of Haematology, London, UK.
  • Nloga AM; King's College London School of Medicine, Department of Haematological Medicine, London, UK.
  • Kulasekararaj AG; King's College London School of Medicine, Department of Haematological Medicine, London, UK.
  • Ades L; Senior Haematology Department, Saint Louis Hospital, APHP, Paris, France.
  • Chomienne C; King's College Hospital, Department of Haematology, London, UK.
  • Fenaux P; Senior Haematology Department, Saint Louis Hospital, APHP, Paris, France.
  • Dosquet C; INSERM, UMRS1131-University Paris Diderot, Saint Louis Hospital, Paris, France.
  • Mufti GJ; Cell Biology Department, Saint Louis Hospital, APHP, Paris, France.
  • Bonnet D; INSERM, UMRS1131-University Paris Diderot, Saint Louis Hospital, Paris, France.
Leukemia ; 31(12): 2702-2708, 2017 12.
Article in En | MEDLINE | ID: mdl-28663577
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.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Myelodysplastic Syndromes / Bone Marrow Cells Type of study: Diagnostic_studies / Prognostic_studies Limits: Animals / Female / Humans / Male Language: En Journal: Leukemia Journal subject: HEMATOLOGIA / NEOPLASIAS Year: 2017 Document type: Article Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Myelodysplastic Syndromes / Bone Marrow Cells Type of study: Diagnostic_studies / Prognostic_studies Limits: Animals / Female / Humans / Male Language: En Journal: Leukemia Journal subject: HEMATOLOGIA / NEOPLASIAS Year: 2017 Document type: Article Country of publication: United kingdom