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Adipogenic Mesenchymal Stromal Cells from Bone Marrow and Their Hematopoietic Supportive Role: Towards Understanding the Permissive Marrow Microenvironment in Acute Myeloid Leukemia
Authors:Yevgeniya Le  Sylvain Fraineau  Priya Chandran  Mitchell Sabloff  Marjorie Brand  Jessie R Lavoie  Rémi Gagne  Michael Rosu-Myles  Carole L Yauk  Richard B Richardson  David S Allan
Institution:1.Canadian Nuclear Laboratories,Chalk River,Canada;2.Regenerative Medicine Program,Ottawa Hospital Research Institute,Ottawa,Canada;3.Department of Medicine,University of Ottawa,Ottawa,Canada;4.Centre for Biologics Evaluation, Biologics and Genetic Therapies Directorate, Health Products and Food Branch,Health Canada,Ottawa,Canada;5.Environmental Health Science and Research Bureau, Healthy Environments and Consumer Safety Branch,Health Canada,Ottawa,Canada;6.McGill Medical Physics Unit,Montreal General Hospital,Montreal,Canada
Abstract:

Purpose

The role of bone marrow-derived mesenchymal stem/stromal cells (MSCs) in creating a permissive microenvironment that supports the emergence and progression of acute myeloid leukemia (AML) is not well established. We investigated the extent to which adipogenic differentiation in normal MSCs alters hematopoietic supportive capacity and we undertook an in-depth comparative study of human bone marrow MSCs derived from newly diagnosed AML patients and healthy donors, including an assessment of adipogenic differentiation capacity.

Findings

MSCs from healthy controls with partial induction of adipogenic differentiation, in comparison to MSCs undergoing partial osteogenic differentiation, expressed increased levels of hematopoietic factors and induced greater proliferation, decreased quiescence and reduced in vitro hematopoietic colony forming capacity of CD34+ hematopoietic stem and progenitor cells (HSPCs). Moreover, we observed that AML-derived MSCs had markedly increased adipogenic potential and delayed osteogenic differentiation, while maintaining normal morphology and viability. AML-derived MSCs, however, possessed reduced proliferative capacity and decreased frequency of subendothelial quiescent MSCs compared to controls.

Conclusion

Our results support the notion of a bone marrow microenvironment characterized by increased propensity toward adipogenesis in AML, which may negatively impact normal hematopoiesis. Larger confirmatory studies are needed to understand the impact of various clinical factors. Novel leukemia treatments aimed at normalizing bone marrow niches may enhance the competitive advantage of normal hematopoietic progenitors over leukemia cells.
Keywords:
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