Preclinical modeling of myelodysplastic syndromes.
K Rouault-PierreS A MianM GoulardA AbarrategiA Di TulioA E SmithA MohamedaliS BestA-M NlogaA G KulasekararajL AdesC ChomienneP FenauxC DosquetG J MuftiDominique BonnetPublished in: Leukemia (2017)
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.
Keyphrases
- bone marrow
- mesenchymal stem cells
- hematopoietic stem cell
- end stage renal disease
- newly diagnosed
- mouse model
- chronic kidney disease
- umbilical cord
- prognostic factors
- peritoneal dialysis
- transcription factor
- stem cells
- case report
- electronic health record
- cell therapy
- low dose
- artificial intelligence
- high dose
- gestational age
- cord blood
- ultrasound guided
- pi k akt