首页> 美国卫生研究院文献>The Journal of Clinical Investigation >Membrane-anchored uPAR regulates the proliferation marrow pool size engraftment and mobilization of mouse hematopoietic stem/progenitor cells
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Membrane-anchored uPAR regulates the proliferation marrow pool size engraftment and mobilization of mouse hematopoietic stem/progenitor cells

机译:膜锚定的uPAR调节增殖骨髓库大小 小鼠造血干/祖细胞的植入和动员 细胞

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摘要

The mechanisms of BM hematopoietic stem/progenitor cell (HSPC) adhesion, engraftment, and mobilization remain incompletely identified. Here, using WT and transgenic mice, we have shown that membrane-anchored plasminogen activator, urokinase receptor (MuPAR) marks a subset of HSPCs and promotes the preservation of the size of this pool of cells in the BM. Loss or inhibition of MuPAR increased HSPC proliferation and impaired their homing, engraftment, and adhesion to the BM microenvironment. During mobilization, MuPAR was inactivated by plasmin via proteolytic cleavage. Cell-autonomous loss of the gene encoding MuPAR also impaired long-term engraftment and multilineage repopulation in primary and secondary recipient mice. These findings identify MuPAR and plasmin as regulators of the proliferation, marrow pool size, homing, engraftment, and mobilization of HSPCs and possibly also of HSCs.
机译:BM造血干/祖细胞(HSPC)粘附,植入和动员的机制仍未完全确定。在这里,我们使用野生型和转基因小鼠表明,膜锚定的纤溶酶原激活物,尿激酶受体( M uPAR)标记了HSPC的一个子集,并促进了该细胞池中的保存。 BM。 M uPAR的丢失或抑制会增加HSPC增殖,并损害其归巢,移入以及对BM微环境的粘附。动员期间,纤溶酶通过蛋白水解切割使 M uPAR失活。 M uPAR编码基因的细胞自主性丧失也损害了原代和次代受体小鼠的长期植入和多系再繁殖。这些发现确定 M uPAR和纤溶酶是HSPCs以及HSCs增殖,骨髓库大小,归巢,移入和动员的调节因子。

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