De La Luz Sierra Maria, Gasperini Paola, McCormick Peter J, Zhu Jinfang, Tosato Giovanna
Laboratory of Cellular Oncology, Center for Cancer Research, National Cancer Institute (NCI), National Institutes of Health (NIH), Bethesda, MD 20892, USA.
Blood. 2007 Oct 1;110(7):2276-85. doi: 10.1182/blood-2007-03-081448. Epub 2007 Jun 27.
The mechanisms underlying granulocyte-colony stimulating factor (G-CSF)-induced mobilization of granulocytic lineage cells from the bone marrow to the peripheral blood remain elusive. We provide evidence that the transcriptional repressor growth factor independence-1 (Gfi-1) is involved in G-CSF-induced mobilization of granulocytic lineage cells from the bone marrow to the peripheral blood. We show that in vitro and in vivo G-CSF promotes expression of Gfi-1 and down-regulates expression of CXCR4, a chemokine receptor essential for the retention of hematopoietic stem cells and granulocytic cells in the bone marrow. Gfi-1 binds to DNA sequences upstream of the CXCR4 gene and represses CXCR4 expression in myeloid lineage cells. As a consequence, myeloid cell responses to the CXCR4 unique ligand SDF-1 are reduced. Thus, Gfi-1 not only regulates hematopoietic stem cell function and myeloid cell development but also probably promotes the release of granulocytic lineage cells from the bone marrow to the peripheral blood by reducing CXCR4 expression and function.
粒细胞集落刺激因子(G-CSF)诱导骨髓中的粒细胞系细胞动员至外周血的潜在机制仍不清楚。我们提供的证据表明,转录抑制因子生长因子独立性-1(Gfi-1)参与了G-CSF诱导的骨髓粒细胞系细胞向外周血的动员。我们发现,在体外和体内,G-CSF均促进Gfi-1的表达,并下调CXCR4的表达,CXCR4是一种趋化因子受体,对造血干细胞和粒细胞保留在骨髓中至关重要。Gfi-1与CXCR4基因上游的DNA序列结合,并抑制髓系细胞系中CXCR4的表达。结果,髓系细胞对CXCR4独特配体SDF-1的反应降低。因此,Gfi-1不仅调节造血干细胞功能和髓系细胞发育,还可能通过降低CXCR4的表达和功能促进骨髓粒细胞系细胞向外周血的释放。