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内皮细胞衍生的细胞外囊泡通过血栓弹力描记术检测到的大小依赖性促凝活性。

Endothelial Cell-derived Extracellular Vesicles Size-dependently Exert Procoagulant Activity Detected by Thromboelastometry.

机构信息

Ludwig Boltzmann Institute for Experimental and Clinical Traumatology, AUVA Research Centre, Vienna, Austria.

Austrian Cluster for Tissue Regeneration, Vienna, Austria.

出版信息

Sci Rep. 2017 Jun 16;7(1):3707. doi: 10.1038/s41598-017-03159-0.

Abstract

Endothelial cells (ECs) are major modulators of hemostasis by expressing and releasing pro- and anticoagulant mediators into the circulation. Previous studies showed that cultured ECs release procoagulant mediators into cell culture supernatants as evidenced by the reduction of viscoelastic clotting time. This effect was reversed with an anti-tissue factor antibody. Here, we aimed to investigate whether tissue factor (TF) was released by endothelial-derived extracellular vesicles (EVs) and which portion of the released vesicles displays the most prominent procoagulant properties. After stimulation of ECs with tumor-necrosis factor-α (TNF-α) the supernatants of EC cultures were subjected to differential centrifugation steps to collect larger and smaller EVs which were then characterised by nanoparticle tracking analysis (NTA) and flow cytometry. Mixed with fresh human blood and analysed by thromboelastometry EVs exerted a significant procoagulant stimulus, which could be partly reversed by addition of an anti-TF antibody. Moreover, TF activity was confirmed in the centrifuged fractions. In summary, our results provide evidence of the procoagulant potential of smaller and larger endothelial-derived EV fractions detected by thromboelastometry. The observed effect is most likely due to the release of TF-bearing EVs of different dimensions, which are released upon TNF-α stimulation of endothelial cell cultures.

摘要

内皮细胞 (ECs) 通过在循环中表达和释放促凝和抗凝介质来调节止血。先前的研究表明,培养的 ECs 将促凝介质释放到细胞培养上清液中,这可以通过粘性凝固时间的缩短来证明。这种效应可以被抗组织因子抗体逆转。在这里,我们旨在研究组织因子 (TF) 是否由内皮细胞衍生的细胞外囊泡 (EVs) 释放,以及释放的囊泡的哪一部分显示出最显著的促凝特性。在用肿瘤坏死因子-α (TNF-α) 刺激 EC 后,EC 培养物的上清液经过差速离心步骤以收集较大和较小的 EVs,然后通过纳米颗粒跟踪分析 (NTA) 和流式细胞术进行表征。与新鲜人血混合并通过血栓弹性描记术分析时,EVs 产生了显著的促凝刺激,这可以通过添加抗 TF 抗体部分逆转。此外,在离心的部分中证实了 TF 活性。总之,我们的结果提供了证据,证明通过血栓弹性描记术检测到较小和较大的内皮细胞衍生 EV 部分具有促凝潜力。观察到的效应很可能是由于不同大小的携带 TF 的 EV 的释放,这些 EV 是在 TNF-α 刺激内皮细胞培养物时释放的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/399e/5473891/f3b773aef599/41598_2017_3159_Fig1_HTML.jpg

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