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脱落的内皮细胞和微粒作为组织因子活性的来源。

Detached endothelial cells and microparticles as sources of tissue factor activity.

作者信息

Kushak Rafail I, Nestoridi Eirini, Lambert Jack, Selig Martin K, Ingelfinger Julie R, Grabowski Eric F

机构信息

Pediatric Hematology/Oncology, MassGeneral Hospital for Children, Harvard Medical School, Boston, MA 02114, USA.

出版信息

Thromb Res. 2005;116(5):409-19. doi: 10.1016/j.thromres.2005.01.013. Epub 2005 Apr 12.

Abstract

INTRODUCTION

Cytokine activation of endothelial cell monolayers is associated with cell detachment, microparticle shedding from plasma membranes, and phosphatidylserine appearance in the plasma membrane outer leaflets. While tissue factor expression on activated endothelial cells and microparticles is well documented, the contribution of detached endothelial cells to tissue factor activity is less clear. We studied tissue factor expression and the role of tissue factor pathway inhibitor on adherent and detached endothelial cells and on microparticles following endothelial cell activation with TNF-alpha.

MATERIALS AND METHODS

Detached endothelial cells and microparticles were obtained from cultures of human umbilical vein endothelial cells by differential centrifugation of cell culture supernatant. For microparticle capture, an antibody directed against CD146 was used. Functional tissue factor activity was measured by chromogenic assay and tissue factor antigen by ELISA. Endothelial cell and microparticle morphology was examined by light and transmission electron microscopy.

RESULTS

After cell activation for 22 h, functional tissue factor activity was distributed as follows: 60%, adherent endothelial cells; 35%, detached cells; and 5%, microparticles. Tissue factor protein followed a similar distribution. Cell detachment was 47%. Electron microscopy demonstrated shedding of microparticles with a diameter of 0.1-0.6 mum. Cy3-annexin V revealed increased phosphatidylserine on activated adherent endothelial cells and microparticles. Pre-incubation of adherent and detached endothelial cells and microparticles with anti-tissue factor antibody blocked factor Xa production. Pre-incubation with anti-tissue factor pathway inhibitor antibody increased tissue factor activity of adherent endothelial cells 2.8-fold, detached cells 1.4-fold, and microparticles 45-fold.

CONCLUSIONS

Detached endothelial cells as well as microparticles from activated endothelial cell monolayers express tissue factor activity, and this activity on microparticles is markedly inhibited by microparticle-associated tissue factor pathway inhibitor.

摘要

引言

细胞因子激活内皮细胞单层与细胞脱离、质膜微粒脱落以及质膜外小叶中磷脂酰丝氨酸的出现有关。虽然活化内皮细胞和微粒上组织因子的表达已有充分记录,但脱离的内皮细胞对组织因子活性的贡献尚不清楚。我们研究了肿瘤坏死因子-α激活内皮细胞后,组织因子在贴壁和脱离的内皮细胞以及微粒上的表达情况,以及组织因子途径抑制剂的作用。

材料与方法

通过对细胞培养上清液进行差速离心,从人脐静脉内皮细胞培养物中获得脱离的内皮细胞和微粒。为捕获微粒,使用了针对CD146的抗体。通过显色测定法测量功能性组织因子活性,通过酶联免疫吸附测定法测量组织因子抗原。通过光学显微镜和透射电子显微镜检查内皮细胞和微粒的形态。

结果

细胞激活22小时后,功能性组织因子活性分布如下:60%存在于贴壁内皮细胞;35%存在于脱离细胞;5%存在于微粒。组织因子蛋白呈现类似的分布。细胞脱离率为47%。电子显微镜显示直径为0.1 - 0.6微米的微粒脱落。Cy3-膜联蛋白V显示活化的贴壁内皮细胞和微粒上的磷脂酰丝氨酸增加。用抗组织因子抗体预孵育贴壁和脱离的内皮细胞以及微粒可阻断Xa因子的产生。用抗组织因子途径抑制剂抗体预孵育可使贴壁内皮细胞的组织因子活性增加2.8倍,脱离细胞增加1.4倍,微粒增加45倍。

结论

脱离的内皮细胞以及活化内皮细胞单层产生的微粒均表达组织因子活性,并且微粒相关的组织因子途径抑制剂可显著抑制微粒上的这种活性。

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