Journal article
Hematopoietic stem cell mobilizing agents G-CSF, cyclophosphamide or AMD3100 have distinct mechanisms of action on bone marrow HSC niches and bone formation
IG Winkler, AR Pettit, LJ Raggatt, RN Jacobsen, CE Forristal, V Barbier, B Nowlan, A Cisterne, LJ Bendall, NA Sims, JP Lévesque
Leukemia | Published : 2012
DOI: 10.1038/leu.2012.17
Abstract
The CXCR4 antagonist AMD3100 is progressively replacing cyclophosphamide (CYP) as adjuvant to granulocyte colony-stimulating factor (G-CSF) to mobilize hematopoietic stem cells (HSC) for autologous transplants in patients who failed prior mobilization with G-CSF alone. It has recently emerged that G-CSF mediates HSC mobilization and inhibits bone formation via specific bone marrow (BM) macrophages. We compared the effect of these three mobilizing agents on BM macrophages, bone formation, osteoblasts, HSC niches and HSC reconstitution potential. Both G-CSF and CYP suppressed niche-supportive macrophages and osteoblasts, and inhibited expression of endosteal cytokines resulting in major impair..
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Awarded by Jet Propulsion Laboratory
Funding Acknowledgements
During the course of this study, JPL was supported by a Senior Research Fellowship from the Cancer Council Queensland, IGW, LJB, and ARP by Career Development Award fellowships and NAS by a Senior Research Fellowship from the National Health and Medical Research Council (NHMRC #488817, #511965, #519744 and #345401, respectively), RNJ by an Australian Post-Graduate Award. This work was supported by NHMRC Project Grants #434515 to JPL and IGW, #345401 to LJR and ARP, and an Anthony Rothe Grant to LJB.