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首页> 外文期刊>Blood: The Journal of the American Society of Hematology >Phagocytosis by macrophages and endothelial cells inhibits procoagulant and fibrinolytic activity of acute promyelocytic leukemia cells
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Phagocytosis by macrophages and endothelial cells inhibits procoagulant and fibrinolytic activity of acute promyelocytic leukemia cells

机译:巨噬细胞和内皮细胞的吞噬作用抑制了急性早幼粒细胞白血病细胞的促凝血和纤溶活性

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摘要

The coagulopathy of acute promyelocytic leukemia (APL) is mainly related to procoagulant substances and fibrinolytic activators of APL blasts, but the fate of these leukemic cells is unknown. The aim of this study was to investigate the removal of APL blasts by macrophages and endothelial cells in vitro and consequent procoagulant and fibrinolytic activity of APL cells.We found that human umbilical vein endothelial cells as well as THP-1 and monocyte-derived macrophages bound, engulfed, and subsequently degraded immortalized APL cell line NB4 and primary APL cells. Lactadherin promoted phagocytosis of APL cells in a time-dependent fashion. Furthermore, factor Xa and prothrombinase activity of phosphatidylserine-exposed target APL cells was time-dependently decreased after incubation with phagocytes (THP-1-derived macrophages or HUVECs). Thrombin production on target APL cells was reduced by40%-45%after 2 hours of coincubation with phagocytes and80%by a combination of lactadherin and phagocytes. Moreover, plasmin generation of target APL cells was inhibited 30% by 2 hours of phagocytosis and ~50% by lactadherin-mediated engulfment. These results suggest that engulfment by macrophages and endothelial cells reduce procoagulant and fibrinolytic activity of APL blasts. Lactadherin and phagocytosis could cooperatively ameliorate the clotting disorders in APL.
机译:急性早幼粒细胞白血病(APL)的凝血病主要与APL母细胞的促凝血物质和纤溶激活剂有关,但这些白血病细胞的命运尚不清楚。这项研究的目的是研究巨噬细胞和内皮细胞在体外对APL母细胞的去除以及由此产生的APL细胞的促凝血和纤溶活性。我们发现人脐静脉内皮细胞以及THP-1和单核细胞衍生的巨噬细胞结合了,吞噬,并随后降解永生的APL细胞系NB4和原代APL细胞。乳粘附素以时间依赖性方式促进APL细胞的吞噬作用。此外,与吞噬细胞(THP-1衍生的巨噬细胞或HUVEC)孵育后,暴露于磷脂酰丝氨酸的目标APL细胞的Xa因子和凝血酶原活性呈时间依赖性降低。与吞噬细胞共同孵育2小时后,目标APL细胞上的凝血酶产生减少了40%-45%,而乳黏附素和吞噬细胞的组合则使凝血酶产生减少了80%。此外,吞噬2小时后,目标APL细胞的纤溶酶生成被抑制了30%,而乳黏附素介导的吞噬抑制了约50%。这些结果表明,巨噬细胞和内皮细胞的吞噬降低了APL母细胞的促凝血和纤溶活性。乳粘附素和吞噬作用可以协同改善APL中的凝血障碍。

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