首页> 外文期刊>Transplantation: Official Journal of the Transplantation Society >Expression of tissue factor and initiation of clotting by human platelets and monocytes after incubation with porcine endothelial cells.
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Expression of tissue factor and initiation of clotting by human platelets and monocytes after incubation with porcine endothelial cells.

机译:与猪内皮细胞孵育后,组织因子的表达以及人血小板和单核细胞的凝结开始。

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OBJECTIVES: Intravascular thrombosis remains a major barrier to successful pig-to-primate xenotransplantation. However, the precise factors initiating thrombosis are unknown. In this study, we investigated the contribution of recipient platelets and monocytes. METHODS: Primary pig aortic endothelial cells (PAECs) were incubated with combinations of fresh or heat-inactivated human plasma, platelets, or monocytes, after which they were separated and analyzed individually by flow cytometry for tissue factor (TF) expression and for their ability to clot recalcified normal or factor-VII-deficient plasma. RESULTS: Procoagulant porcine TF was induced in PAECs only by fresh human plasma, and not by heat-inactivated plasma, platelets, or monocytes. In contrast, procoagulant human TF was induced on platelets and monocytes after incubation with PAEC, irrespective of whether the plasma was present or not. In addition, human platelets caused the shedding of procoagulant TF-expressing aggregates from PAEC. CONCLUSIONS: This work defines a cell-based in vitro assay system to address complex interactions among PAECs, human platelets, and monocytes. The induction of procoagulant TF on PAECs by fresh human plasma was most likely dependent on xenoreactive natural antibody and complement present in fresh human plasma. In contrast, the shedding of procoagulant platelet-PAEC aggregates, induced by human platelets, and the induction of procoagulant TF on human platelets and monocytes by PAEC, occurred independently of these factors. These results suggest that different mechanisms may contribute to the initiation of thrombosis after xenotransplantation, some of which may not be influenced by the further manipulation of the immune response against pig xenografts.
机译:目的:血管内血栓形成仍然是成功进行猪到灵长类动物异种移植的主要障碍。但是,尚不清楚引发血栓形成的确切因素。在这项研究中,我们调查了受体血小板和单核细胞的贡献。方法:将原代猪主动脉内皮细胞(PAEC)与新鲜或热灭活的人血浆,血小板或单核细胞组合孵育,然后分离并通过流式细胞术分别分析组织因子(TF)的表达及其功能凝结重新钙化的正常血浆或缺乏VII因子的血浆。结果:PAECs中的促凝猪TF仅由新鲜的人血浆诱导,而不是由热灭活的血浆,血小板或单核细胞诱导。相反,在与PAEC孵育后,血小板和单核细胞上促凝的人TF诱导产生,而与血浆是否存在无关。另外,人血小板引起PAEC表达促凝TF的聚集体脱落。结论:这项工作定义了一种基于细胞的体外测定系统,以解决PAEC,人类血小板和单核细胞之间的复杂相互作用。新鲜人血浆对PAECs促凝血因子TF的诱导很可能取决于异反应性天然抗体和新鲜人血浆中存在的补体。相反,由人的血小板引起的促凝血小板-PAEC聚集体的脱落和由PAEC对人的血小板和单核细胞的促凝血TF的诱导独立于这些因素而发生。这些结果表明,不同的机制可能有助于异种移植后血栓形成的开始,其中某些机制可能不受针对猪异种移植物的免疫反应的进一步操纵的影响。

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