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血管性血友病因子病在内皮祖细胞中的特异性缺陷和蛋白质组学特征。

von Willebrand disease-specific defects and proteomic signatures in endothelial colony-forming cells.

作者信息

Laan Sebastiaan N J, Groten Stijn, Dirven Richard J, Bürgisser Petra E, Leebeek Frank W G, van Moort Iris, van den Biggelaar Maartje, Bierings Ruben, Eikenboom Jeroen

机构信息

Department of Internal Medicine, Division of Thrombosis and Hemostasis, Leiden University Medical Centre, Leiden, the Netherlands; Department of Hematology, Erasmus University Medical Centre, Rotterdam, the Netherlands.

Department of Molecular Hematology, Sanquin Research, Amsterdam, the Netherlands.

出版信息

J Thromb Haemost. 2025 Aug;23(8):2634-2650. doi: 10.1016/j.jtha.2025.04.024. Epub 2025 May 6.

Abstract

BACKGROUND

Endothelial cells are crucial for hemostasis as they produce von Willebrand factor (VWF). von Willebrand disease (VWD) results from a deficiency of, or defects in, VWF.

OBJECTIVES

We analyzed the endothelial compartment of VWD patients with an unexplained decrease in VWF level or nonresponse to 1-8-deamino-D-arginine vasopressin (DDAVP) using endothelial colony-forming cells (ECFCs).

METHODS

Thirteen healthy controls and 10 VWD type 1 and 2 patients were included, and a total of 29 ECFC clones were obtained. Plasma was analyzed, and ECFCs were morphologically and functionally characterized by quantitative polymerase chain reaction, ELISA, imaging, migration assay, and mass spectrometry.

RESULTS

VWF plasma levels were reduced in all patients. ECFCs were categorized into 2 previously defined transcriptional clusters and matched between patients and controls. Four ECFC clones, all from DDAVP nonresponders, retained VWF in the endoplasmic reticulum. Cluster 1 ECFCs from DDAVP nonresponders closed more slowly in the migration assay and had lower basal release of VWF antigen than control ECFCs. Proteomic data of ECFC lysates showed overlap in clustering with RNA profiles, including ALDHA1, TGFB1, and other endothelial-to-mesenchymal/inflammatory markers. However, no patient group-specific phenotype was observed. Finally, regulated secretion of VWF and Weibel-Palade body count in ECFCs correlated with various secretory machinery components.

CONCLUSION

Lower plasma VWF was linked to reduced production and secretion by ECFCs obtained from patients. Furthermore, nonresponse to DDAVP in some patients was explained by VWF retention in the endoplasmic reticulum. The correlation between functional aspects of ECFCs and their quantitative polymerase chain reaction and proteome profiles yielded potential targets for further research.

摘要

背景

内皮细胞对于止血至关重要,因为它们能产生血管性血友病因子(VWF)。血管性血友病(VWD)是由VWF缺乏或缺陷引起的。

目的

我们使用内皮祖细胞集落形成细胞(ECFCs)分析了血管性血友病因子水平不明原因降低或对1-8-去氨基-D-精氨酸血管加压素(DDAVP)无反应的血管性血友病患者的内皮细胞区室。

方法

纳入13名健康对照者以及10名1型和2型血管性血友病患者,共获得29个ECFC克隆。对血浆进行分析,并通过定量聚合酶链反应、酶联免疫吸附测定、成像、迁移试验和质谱对ECFCs进行形态学和功能特征分析。

结果

所有患者的血浆VWF水平均降低。ECFCs被分为2个先前定义的转录簇,患者和对照者之间相匹配。4个ECFC克隆(均来自对DDAVP无反应者)的VWF保留在内质网中。来自对DDAVP无反应者的1型簇ECFCs在迁移试验中闭合更慢,并且VWF抗原的基础释放量低于对照ECFCs。ECFC裂解物的蛋白质组学数据显示,在聚类方面与RNA谱存在重叠,包括醛脱氢酶1(ALDHA1)、转化生长因子β1(TGFB1)和其他内皮向间充质/炎症标志物。然而,未观察到患者组特异性表型。最后,ECFCs中VWF的调节性分泌和魏-帕小体计数与各种分泌机制成分相关。

结论

较低的血浆VWF与患者来源的ECFCs产生和分泌减少有关。此外,一些患者对DDAVP无反应可通过VWF保留在内质网来解释。ECFCs功能方面与其定量聚合酶链反应和蛋白质组谱之间的相关性产生了进一步研究的潜在靶点。

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