Wang J F, Liu Z Y, Groopman J E
Divisions of Experimental Medicine and Hematology/Oncology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.
Blood. 1998 Aug 1;92(3):756-64.
CXCR4 is the receptor for the alpha-chemokine stromal cell-derived factor 1 (SDF-1) and has been shown to be expressed on a diversity of leukocytes. In this report, the expression of the CXCR4 receptor in cells of megakaryocytic lineage and the role of SDF-1 in megakaryocytopoiesis were investigated. Using flow cytometry in combination with reverse transcriptase-polymerase chain reaction (RT-PCR), we observed that bone marrow CD34(+), CD61(+) cells, blood platelets, and megakaryocytic leukemia cell lines all expressed the CXCR4 receptor. To examine the expression of the CXCR4 receptor on megakaryocyte progenitors (colony-forming units-megakaryocyte [CFU-Meg]), CXCR4-positive and -negative CD34(+) populations were separated from bone marrow and cultured in a plasma clot culture system. A subpopulation of the CFU-Meg was found in the CXCR4-positive fraction. The functional significance of CXCR4 expression on cells of the megakaryocytic lineage was examined by studying the effects of SDF-1alpha on migration and proliferation of megakaryocyte progenitor cells in vitro. We found that SDF-1alpha potently induced megakaryocyte progenitor migration and significantly enhanced adhesion of mature marrow megakaryocytes to endothelium. No marked effects of SDF-1alpha alone or in combination with thrombopoietin and stem cell factor/kit ligand on megakaryocyte production in vitro were noted. These results demonstrate for the first time that the CXCR4 alpha-chemokine receptor is expressed on cells of the megakaryocytic lineage from progenitors to platelets and that its ligand SDF-1alpha may modulate several aspects of megakaryocytopoiesis.
CXCR4是α趋化因子基质细胞衍生因子1(SDF-1)的受体,已证实在多种白细胞上表达。在本报告中,研究了CXCR4受体在巨核细胞系细胞中的表达以及SDF-1在巨核细胞生成中的作用。通过流式细胞术结合逆转录聚合酶链反应(RT-PCR),我们观察到骨髓CD34(+)、CD61(+)细胞、血小板和巨核细胞白血病细胞系均表达CXCR4受体。为检测巨核细胞祖细胞(集落形成单位-巨核细胞[CFU-Meg])上CXCR4受体的表达,从骨髓中分离出CXCR4阳性和阴性的CD34(+)群体,并在血浆凝块培养系统中培养。在CXCR4阳性部分发现了CFU-Meg的一个亚群。通过研究SDF-1α对体外巨核细胞祖细胞迁移和增殖的影响,检测了CXCR4在巨核细胞系细胞上表达的功能意义。我们发现SDF-1α强烈诱导巨核细胞祖细胞迁移,并显著增强成熟骨髓巨核细胞与内皮细胞的黏附。未观察到SDF-1α单独或与血小板生成素和干细胞因子/kit配体联合对体外巨核细胞生成有明显影响。这些结果首次证明CXCR4α趋化因子受体在从祖细胞到血小板的巨核细胞系细胞上表达,其配体SDF-1α可能调节巨核细胞生成的多个方面。