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Hematopoietic Stem Cell Mobilization and Homing after Transplantation: The Role of MMP-2 MMP-9 and MT1-MMP

机译:造血干细胞动员和移植后归巢:MMP-2MMP-9和MT1-MMP的作用

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摘要

Hematopoietic stem/progenitor cells (HSPCs) are used in clinical transplantation to restore hematopoietic function. Here we review the role of the soluble matrix metalloproteinases MMP-2 and MMP-9, and membrane type (MT)1-MMP in modulating processes critical to successful transplantation of HSPC, such as mobilization and homing. Growth factors and cytokines which are employed as mobilizing agents upregulate MMP-2 and MMP-9. Recently we demonstrated that MT1-MMP enhances HSPC migration across reconstituted basement membrane, activates proMMP-2, and contributes to a highly proteolytic bone marrow microenvironment that facilitates egress of HSPC. On the other hand, we reported that molecules secreted during HSPC mobilization and collection, such as hyaluronic acid and thrombin, increase MT1-MMP expression in cord blood HSPC and enhance (prime) their homing-related responses. We suggest that modulation of MMP-2, MMP-9, and MT1-MMP expression has potential for development of new therapies for more efficient mobilization, homing, and engraftment of HSPC, which could lead to improved transplantation outcomes.
机译:造血干/祖细胞(HSPC)用于临床移植以恢复造血功能。在这里,我们回顾了可溶性基质金属蛋白酶MMP-2和MMP-9,以及膜类型(MT)1-MMP在成功移植HSPC至关重要的调节过程中的作用,例如动员和归巢。用作动员剂的生长因子和细胞因子上调MMP-2和MMP-9。最近,我们证明MT1-MMP增强了HSPC跨重构的基底膜的迁移,激活了proMMP-2,并促进了高度蛋白水解的骨髓微环境,从而促进了HSPC的流出。另一方面,我们报道了在HSPC动员和收集过程中分泌的分子,例如透明质酸和凝血酶,会增加脐带血HSPC中MT1-MMP的表达,并增强(启动)其归巢相关反应。我们建议调节MMP-2,MMP-9和MT1-MMP的表达具有开发新疗法的潜力,以更有效地动员,归巢和植入HSPC,这可能会改善移植结果。

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