Abstract

G-CSF is the most widely used agent in the clinical setting to induce the mobilization of HPC. Several recent studies have shown that G-CSF treatment results in decreased SDF-1 protein expression in the bone marrow (BM). Moreover, functional expression of CXCR4 on HPC mobilized into the blood by G-CSF is reduced relative to HPC in the bone marrow. Given its importance in regulating HPC trafficking in the bone marrow, these data suggest that disruption of SDF-1/CXCR4 signaling is a key step in G-CSF induced HPC mobilization. In addition to G-CSF, there are many other cytokines that can induce HPC mobilization. Though the cellular targets and biological activities of mobilizing cytokines are diverse, it is possible that disruption of SDF-1/CXCR4 signaling is a common shared mechanisms of HPC mobilization. To test this hypothesis, we characterized SDF-1 and CXCR4 expression in mice treated with flt-3 ligand or stem cell factor (SCF), two cytokines that induce HPC mobilization in both mice and humans. C57BL/6 mice (n=6–8, each) were treated with human flt-3 ligand (10 mg per day x 7 days) or pegylated-rat SCF (200 mg/kg/day x 7 days). As previously reported, both cytokines induced robust HPC mobilization [number of CFU-C per ml of blood ± SEM: 17,000 ± 795 (SCF); >40,000 (flt-3 ligand); 138 ± 63 (saline)]. At the time of peak mobilization, mice were sacrificed and SDF-1 protein in the bone marrow measured by ELISA. Both flt-3 ligand- and SCF-treated mice showed significant reduction in SDF-1 protein compared with untreated controls [percent reduction ± SEM: 64% ± 12% (flt-3 ligand), 79% ± 10% (SCF)].

We next determined whether SDF-1 expression in the bone marrow during flt-3 ligand and SCF induced mobilization is primarily regulated at an mRNA level, similar to G-CSF. Isolated femurs were directly flushed with Trizol and SDF-1 mRNA was measured using a real time RT-PCR assay. The amount SDF-1 mRNA with respect to beta-actin mRNA was reduced in both flt-3 ligand- and SCF-treated mice compared with the untreated controls [percent reduction ± SEM: 79% ± 8% (flt-3 ligand), 60% ± 24% (SCF)].

Finally, we determined whether functional CXCR4 expression of mobilized HPC decreased during flt-3 and SCF induced mobilization. A transwell migration assay was used to measure the percentage of BM and blood HPC that migrated in response to SDF-1. As reported previously, the percentage of blood HPC that migrated to SDF-1 was significantly decreased compared with BM HPC in G-CSF treated mice [percent migrated ± SEM: 9.6 ± 3.0% (blood) and 16.2 ± 1.2% (BM)]. A similar trend was observed in flt-3 ligand treated [5% ± 4% (blood) and 32 ± 9% (BM)] and SCF treated mice [2.0 ± 2% (blood) and 21 ± 8% (BM)]. Collectively, these data show that during flt-3 ligand and SCF induced HPC mobilization SDF-1/CXCR4 signaling is disrupted. Similar to G-CSF, both of these agents primarily regulate SDF-1 expression in the BM at an mRNA level. In addition, functional expression of CXCR4 on mobilized HPC is decreased. These data suggest the hypothesis that disruption of SDF-1/CXCR4 signaling may be a common mechanism by which all hematopoietic cytokines induce HPC mobilization.

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