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外周血干细胞动员:CXCR2配体GROβ可快速动员具有增强植入特性的造血干细胞。

Peripheral blood stem cell mobilization: the CXCR2 ligand GRObeta rapidly mobilizes hematopoietic stem cells with enhanced engraftment properties.

作者信息

Pelus Louis M, Fukuda Seiji

机构信息

Department of Microbiology and Immunology and the Walther Oncology Center, Indiana University School of Medicine and the Walther Cancer Institute, Indianapolis, IN 46202 USA.

出版信息

Exp Hematol. 2006 Aug;34(8):1010-20. doi: 10.1016/j.exphem.2006.04.004.

Abstract

Chemokines direct the movement of leukocytes, including hematopoietic stem and progenitor cells, and can mobilize hematopoietic cells from marrow to peripheral blood where they can be used for transplantation. In this review, we will discuss the stem cell mobilizing activities and mechanisms of action of GRObeta, a CXC chemokine ligand for the CXCR2 receptor. GRObeta rapidly mobilizes short- and long-term repopulating cells in mice and/or monkeys and synergistically enhances mobilization responses when combined with the widely used clinical mobilizer, granulocyte colony-stimulating factor (G-CSF). The hematopoietic graft mobilized by GRObeta contains significantly more CD34(neg), Sca-1+, c-kit+, lineage(neg) (SKL) cells than the graft mobilized by G-CSF. In mice, stem cells mobilized by GRObeta demonstrate a competitive advantage upon long-term repopulation analysis and restore neutrophil and platelet counts significantly faster than cells mobilized by G-CSF. Even greater advantage in repopulation and restoration of hematopoiesis are observed with stem cells mobilized by the combination of GRObeta and G-CSF. GRObeta-mobilized SKL cells demonstrate enhanced adherence to vascular cell adhesion molecule-1 and VCAM(pos) endothelial cells and home more efficiently to bone marrow in vivo. The marrow homing ability of GRObeta-mobilized cells is less dependent on the CXCR4/SDF-1 axis than cells mobilized by G-CSF. The mechanism of mobilization by GRObeta requires active matrix metalloproteinase-9 (MMP-9), which results from release of pro-MMP-9 from peripheral blood, and marrow neutrophils, which alters the stoichiometry between pro-MMP-9 and its inhibitor tissue inhibitor of metalloproteinase-1, resulting in MMP-9 activation. The efficacy and rapid action of GRObeta and lack of proinflammatory activity make it an attractive agent to supplement mobilization by G-CSF. In addition, GRObeta may also have clinical mobilizing efficacy on its own, reducing the overall time and costs associated with peripheral blood stem cell transplantation.

摘要

趋化因子可引导包括造血干细胞和祖细胞在内的白细胞移动,并能将造血细胞从骨髓动员至外周血,以便用于移植。在本综述中,我们将讨论GROβ(一种CXCR2受体的CXC趋化因子配体)的干细胞动员活性及作用机制。GROβ能迅速动员小鼠和/或猴子体内的短期和长期重建造血细胞,并且在与广泛应用于临床的动员剂粒细胞集落刺激因子(G-CSF)联合使用时,可协同增强动员反应。由GROβ动员的造血移植物中所含的CD34阴性、Sca-1阳性、c-kit阳性、谱系阴性(SKL)细胞比由G-CSF动员的移植物显著更多。在小鼠中,经长期重建造血分析,由GROβ动员的干细胞显示出竞争优势,并且其恢复中性粒细胞和血小板计数的速度明显快于由G-CSF动员的细胞。在由GROβ和G-CSF联合动员的干细胞中,观察到在重建造血和恢复造血方面具有更大优势。由GROβ动员的SKL细胞显示出对血管细胞黏附分子-1和VCAM阳性内皮细胞的黏附增强,并且在体内能更有效地归巢至骨髓。与由G-CSF动员的细胞相比,由GROβ动员的细胞的骨髓归巢能力对CXCR4/SDF-1轴的依赖性较小。GROβ的动员机制需要活性基质金属蛋白酶-9(MMP-9),这是由外周血中前MMP-9的释放以及骨髓中性粒细胞引起的,骨髓中性粒细胞会改变前MMP-9与其抑制剂金属蛋白酶组织抑制剂-1之间的化学计量关系,从而导致MMP-9激活。GROβ的有效性和快速作用以及缺乏促炎活性使其成为补充G-CSF动员的有吸引力的药物。此外,GROβ自身可能也具有临床动员效果,可减少与外周血干细胞移植相关的总体时间和成本。

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