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Blood, 15 March 2004, Vol. 103, No. 6, pp. 2071-2078.
Prepublished online as a Blood First Edition Paper on November 6, 2003; DOI 10.1182/blood-2003-06-2099.
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HEMATOPOIESIS
Mobilization studies in mice deficient in either C3 or C3a receptor (C3aR) reveal a novel role for complement in retention of hematopoietic stem/progenitor cells in bone marrow
Janina Ratajczak,
Ryan Reca,
Magda Kucia,
Marcin Majka,
Daniel J. Allendorf,
Jarek T. Baran,
Anna Janowska-Wieczorek,
Rick A. Wetsel,
Gordon D. Ross, and
Mariusz Z. Ratajczak
From the Stem Cell Biology Program, James Graham Brown Cancer Center, University of Louisville, Louisville, KY; the Department of Medicine, University of Alberta and Canadian Blood Services, Edmonton, AB, Canada; the European Stem Cell Therapeutic Excellence Center, Medical College, Jagiellonian University, Cracow, Poland; and the Institute of Molecular Medicine, University of TexasHouston, Houston, TX.
The mechanisms regulating the homing/mobilization of hematopoietic stem/progenitor cells (HSPCs) are not fully understood. In our previous studies we showed that the complement C3 activation peptide, C3a, sensitizes responses of HSPCs to stromal-derived factor 1 (SDF-1). In this study, mobilization was induced with granulocyte colony-stimulating factor (G-CSF) in both C3-deficient (C3/) and C3a receptordeficient (C3aR/) mice as well as in wild-type (wt) mice in the presence or absence of a C3aR antagonist, SB 290157. The data indicated (1) significantly increased G-CSFinduced mobilization in C3/ and C3aR/ mice compared with wt mice, (2) significantly accelerated and enhanced G-CSFinduced mobilization in wt, but not in C3/ or C3aR/, mice treated with SB 290157, and (3) deposition of C3b/iC3b fragments onto the viable bone marrow (BM) cells of G-CSFtreated animals. Furthermore, mobilization studies performed in chimeric mice revealed that wt mice reconstituted with C3aR/ BM cells, but not C3aR/ mice reconstituted with wt BM cells, are more sensitive to G-CSFinduced mobilization, suggesting that C3aR deficiency on graft-derived cells is responsible for this increased mobilization. Hence we suggest that C3 is activated in mobilized BM into C3a and C3b, and that the C3a-C3aR axis plays an important and novel role in retention of HSPCs (by counteracting mobilization) by increasing their responsiveness to SDF-1, the concentration of which is reduced in BM during mobilization. The C3a-C3aR axis may prevent an uncontrolled release of HSPCs into peripheral blood. These data further suggest that the C3aR antagonist SB 290157 could be developed as a drug to mobilize HSPCs for transplantation.

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