Petit Isabelle, Szyper-Kravitz Martine, Nagler Arnon, Lahav Meir, Peled Amnon, Habler Liliana, Ponomaryov Tanya, Taichman Russell S, Arenzana-Seisdedos Fernando, Fujii Nobutaka, Sandbank Judith, Zipori Dov, Lapidot Tsvee
Department of Immunology, The Weizmann Institute of Science, Rehovot, Israel.
Nat Immunol. 2002 Jul;3(7):687-94. doi: 10.1038/ni813. Epub 2002 Jun 17.
Granulocyte colony-stimulating factor (G-CSF) induced hematopoietic stem cell mobilization is widely used for clinical transplantation; however, the mechanism is poorly understood. We report here that G-CSF induced a reduction of the chemokine stromal cell derived factor 1 (SDF-1) and an increase in its receptor CXCR4 in the bone marrow (BM), whereas their protein expression in the blood was less affected. The gradual decrease of BM SDF-1, due mostly to its degradation by neutrophil elastase, correlated with stem cell mobilization. Elastase inhibition reduced both activities. Human and murine stem cell mobilization was inhibited by neutralizing CXCR4 or SDF-1 antibodies, demonstrating SDF-1 CXCR4 signaling in cell egress. We suggest that manipulation of SDF-1 CXCR4 interactions may be a means with which to control the navigation of progenitors between the BM and blood to improve the outcome of clinical stem cell transplantation.
粒细胞集落刺激因子(G-CSF)诱导的造血干细胞动员广泛应用于临床移植;然而,其机制尚不清楚。我们在此报告,G-CSF诱导骨髓(BM)中趋化因子基质细胞衍生因子1(SDF-1)减少,其受体CXCR4增加,而它们在血液中的蛋白表达受影响较小。骨髓SDF-1的逐渐减少主要是由于其被中性粒细胞弹性蛋白酶降解,这与干细胞动员相关。弹性蛋白酶抑制降低了这两种活性。人源和鼠源干细胞动员被中和CXCR4或SDF-1抗体所抑制,表明SDF-1-CXCR4信号传导参与细胞迁出。我们认为,操纵SDF-1-CXCR4相互作用可能是一种控制祖细胞在骨髓和血液之间迁移的方法,以改善临床干细胞移植的效果。