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Osteoclasts are dispensable for hematopoietic progenitor mobilization by granulocyte colony-stimulating factor in mice
Journal article   Open access   Peer reviewed

Osteoclasts are dispensable for hematopoietic progenitor mobilization by granulocyte colony-stimulating factor in mice

Mahil Rao, Teerawit Supakomdej, Amy P. Schmidt and Daniel C. Link
Experimental hematology, Vol.43(2), pp.110-114
02/01/2015
DOI: 10.1016/j.exphem.2014.10.012
PMCID: PMC4323843
PMID: 25461255
url
https://doi.org/10.1016/j.exphem.2014.10.012View
Published (Version of record) Open Access

Abstract

The contribution of osteoclasts to hematopoietic stem/progenitor cell (HSPC) retention in the bone marrow is controversial. Studies of HSPC trafficking in osteoclast-deficient mice are limited by osteopetrosis. Here, we employed two non-osteopetrotic mouse models to assess the contribution of osteoclasts to basal and granulocyte colony-stimulating factor (G-CSF)-induced HSPC mobilization. We generated Rank(-/-) fetal liver chimeras using Csf3r(-/-) recipients to produce mice lacking G-CSF receptor expression in osteoclasts. Basal and G-CSF-induced HSPC mobilization was normal in these chimeras. We next acutely depleted osteoclasts in wild-type mice using the RANK ligand inhibitor osteoprotegerin. Marked suppression of osteoclasts was observed after a single injection of osteoprotegerin-Fc. Basal and G-CSF-induced HSPC mobilization in osteoprotegerin-Fc-treated mice was comparable to that in control mice. Together, these data indicate that osteoclasts are not required for the efficient retention of HSPCs in the bone marrow and are dispensable for HSPC mobilization by G-CSF. Copyright (C) 2015 ISEH - International Society for Experimental Hematology. Published by Elsevier Inc.
Hematology Life Sciences & Biomedicine Medicine, Research & Experimental Research & Experimental Medicine Science & Technology

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