Tjwa Marc, Sidenius Nicolai, Moura Rute, Jansen Sandra, Theunissen Koen, Andolfo Annapaola, De Mol Maria, Dewerchin Mieke, Moons Lieve, Blasi Francesco, Verfaillie Catherine, Carmeliet Peter
VIB--Vesalius Research Center, Katholieke Universiteit Leuven, Leuven, Belgium.
J Clin Invest. 2009 Apr;119(4):1008-18. doi: 10.1172/JCI36010. Epub 2009 Mar 9.
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.
骨髓造血干细胞/祖细胞(HSPC)的黏附、植入和动员机制尚未完全明确。在此,我们利用野生型和转基因小鼠,证明了膜锚定纤溶酶原激活物尿激酶受体(MuPAR)标记了一部分HSPC,并促进了骨髓中这一细胞群体数量的维持。MuPAR的缺失或抑制会增加HSPC的增殖,并损害其归巢、植入以及与骨髓微环境的黏附。在动员过程中,MuPAR会被纤溶酶通过蛋白水解切割而失活。编码MuPAR的基因在细胞自主缺失时,也会损害初代和二代受体小鼠的长期植入及多谱系重建。这些发现确定了MuPAR和纤溶酶是HSPC以及可能还有造血干细胞增殖、骨髓库大小、归巢、植入和动员的调节因子。