Treatment of circulating CD34 + cells with SDF-1α or anti-CXCR4 antibody enhances migration and NOD/SCID repopulating potential

• Published in: Experimental hematology 2002-09, Vol.30 (9), p.1061-1069
• Main Authors: Plett, P.Artur, Frankovitz, Stacy M, Wolber, Frances M, Abonour, Rafat, Orschell-Traycoff, Christie M
• Format: Article
• Language: English
• ISSN: 0301-472X; 1873-2399
• DOI: 10.1016/S0301-472X(02)00880-9

Stromal cell–derived factor-1α (SDF-1α) has been implicated in homing and engraftment of primitive hematopoietic progenitor cells (HPC) in studies demonstrating reduced NOD/SCID repopulating potential of HPC exposed to supra-physiologic concentrations of SDF-1α or anti-CXCR4. Outcome of CXCR4 signaling in some cells has been shown to be dependent on the concentration of SDF-1α. We aimed to determine whether similar concentration-dependent responses to CXCR4 signaling are present in CD34 +cells. Human peripheral blood (PB), mobilized PB (MPB), or bone marrow (BM) CD34 + cells were incubated for 30 minutes with different concentrations of SDF-1α or anti-CXCR4, washed, then assessed for in vitro hematopoietic potential, migration, and NOD/SCID repopulating potential. Exposure of MPB or PB CD34 + cells to 100 ng/mL SDF-1α increased tyrosine phosphorylation without subsequent proliferation or apoptosis. Spontaneous and SDF-1α-directed migration also increased in pretreated cells, despite previous exposure to SDF-1α. Cells exposed to 1 μg anti-CXCR4/10 6 cells displayed similar increases in activation and migration as cells exposed to SDF-1α, demonstrating the ability of anti-CXCR4 to activate the CXCR4 receptor. Interestingly, chimerism in NOD/SCID mice transplanted with MPB CD34 + cells pretreated with SDF-1α or anti-CXCR4 was increased, while exposure of these cells to 10- to 100-fold higher concentrations of these proteins inhibited in vitro migration and NOD/SCID repopulating potential. Migration and NOD/SCID repopulating potential of BM CD34 + cells remained unchanged after treatment with either protein. These results illustrate the ability of SDF-1α and anti-CXCR4 to augment repopulating potential of CD34 + cells, and suggest that HPC function can be favorably modulated through specific CXCR4 signaling.