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血小板诱导的内皮祖细胞分化。

Platelet-induced differentiation of endothelial progenitor cells.

作者信息

Langer Harald F, May Andreas E, Vestweber Dietmar, De Boer Hetty C, Hatzopoulos Antonis K, Gawaz Meinrad

机构信息

Medizinische Klinik III, Eberhard Karls Universität Tübingen, Tübingen, Germany.

出版信息

Semin Thromb Hemost. 2007 Mar;33(2):136-43. doi: 10.1055/s-2007-969026.

Abstract

Endothelial progenitor cells (EPCs) have the potential to home at sites of vascular lesions and to contribute to revascularization. This homing is a highly concerted mechanism, which involves chemotaxis, adhesion, migration, and finally integration of the cells into the target tissue. Only recently has the platelet been identified as a central mediator of EPC homing. Adherent platelets were able to mediate chemotaxis and adhesion of EPCs, a process that involved P-selectin glycoprotein ligand 1 and very late antigen-4 (VLA-4). Recent studies suggest that platelet-derived stromal cell-derived factor-1 is also involved centrally in the recruitment of EPCs. Furthermore, platelets induce progenitor cell migration by platelet-derived growth factor AB. Recent in vivo data confirm the recruitment of EPCs to sites of vascular lesions after vessel denudation by activated platelets and fibrin. Moreover, when coincubated with platelets, EPCs differentiate to mature endothelial cells and have the potential to migrate and colonize a platelet thrombus. The described interaction of EPCs with platelets represents a novel mechanism of vascular remodeling and healing of endothelial lesions.

摘要

内皮祖细胞(EPCs)具有归巢至血管损伤部位并促进血管再生的潜力。这种归巢是一种高度协调的机制,涉及趋化性、黏附、迁移,最终使细胞整合到靶组织中。直到最近,血小板才被确定为EPC归巢的核心介质。黏附的血小板能够介导EPCs的趋化性和黏附,这一过程涉及P-选择素糖蛋白配体1和极晚期抗原-4(VLA-4)。最近的研究表明,血小板衍生的基质细胞衍生因子-1也在EPCs的募集过程中起核心作用。此外,血小板通过血小板衍生生长因子AB诱导祖细胞迁移。最近的体内数据证实,活化的血小板和纤维蛋白使血管内皮剥脱后,EPCs会募集至血管损伤部位。此外,当与血小板共同孵育时,EPCs会分化为成熟的内皮细胞,并具有迁移至血小板血栓并在其中定植的潜力。所描述的EPCs与血小板之间的相互作用代表了血管重塑和内皮损伤愈合的一种新机制。

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