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聚集的低密度脂蛋白摄取诱导人血管平滑肌细胞膜组织因子促凝活性和微粒释放。

Aggregated low-density lipoprotein uptake induces membrane tissue factor procoagulant activity and microparticle release in human vascular smooth muscle cells.

作者信息

Llorente-Cortés Vicenta, Otero-Viñas Marta, Camino-López Sandra, Llampayas Oriol, Badimon Lina

机构信息

Cardiovascular Research Center, CSIC-ICCC, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.

出版信息

Circulation. 2004 Jul 27;110(4):452-9. doi: 10.1161/01.CIR.0000136032.40666.3D. Epub 2004 Jul 6.

Abstract

BACKGROUND

Tissue factor (TF) is the main initiator of the arterial blood coagulation system, and aggregated LDL (agLDL) are found in the arterial intima. Our hypothesis is that agLDL internalization by vascular smooth muscle cells (VSMCs) may trigger TF-procoagulant activity.

METHODS AND RESULTS

Cultured human VSMCs were obtained from human coronary arteries of explanted hearts during transplant operations. VSMCs were incubated with native LDL (nLDL) or agLDL. TF mRNA was analyzed by real-time polymerase chain reaction, and cellular and released TF protein antigen were analyzed by Western blot. TF microparticle (MP) content was analyzed by flow cytometry and TF activity by a factor Xa generation test. Both nLDL and agLDL strongly and equally increased TF mRNA and cell membrane protein expression, by approximately 5- and 9-fold, respectively. A sustained TF procoagulant activity was induced by agLDL but not by nLDL (agLDL 2.46+/-0.22 versus nLDL 0.72+/-0.12 mU/mg protein at 12 hours). AgLDL increased TF antigen release (agLDL 5.64+/-0.4 versus nLDL 3.28+/-0.22 AU) and TF MP release (agLDL 89.85+/-8.51 versus nLDL 19.69+/-4.59 TF MP/10(3) cells). TF activation and release induced by agLDL is not related to apoptosis. Blockade of LDL receptor-related protein, a receptor for agLDL, prevented the agLDL-induced release of TF protein and TF MP.

CONCLUSIONS

VSMC-TF expression is upregulated by both nLDL and agLDL. However, only agLDL engagement to LDL receptor-related protein induced cellular TF procoagulant activity and TF release by human VSMCs.

摘要

背景

组织因子(TF)是动脉血液凝固系统的主要启动因子,而聚集的低密度脂蛋白(agLDL)存在于动脉内膜中。我们的假设是血管平滑肌细胞(VSMC)内化agLDL可能会触发TF的促凝血活性。

方法与结果

在移植手术期间,从离体心脏的人冠状动脉中获取培养的人VSMC。将VSMC与天然低密度脂蛋白(nLDL)或agLDL一起孵育。通过实时聚合酶链反应分析TF mRNA,通过蛋白质印迹分析细胞内和释放的TF蛋白抗原。通过流式细胞术分析TF微粒(MP)含量,通过因子Xa生成试验分析TF活性。nLDL和agLDL均强烈且同等程度地增加TF mRNA和细胞膜蛋白表达,分别增加约5倍和9倍。agLDL诱导了持续的TF促凝血活性,而nLDL则未诱导(12小时时,agLDL为2.46±0.22,nLDL为0.72±0.12 mU/mg蛋白)。agLDL增加了TF抗原释放(agLDL为5.64±0.4,nLDL为3.28±0.22 AU)和TF MP释放(agLDL为89.85±8.51,nLDL为19.69±4.59 TF MP/10³细胞)。agLDL诱导的TF激活和释放与细胞凋亡无关。阻断agLDL的受体——低密度脂蛋白受体相关蛋白,可防止agLDL诱导的TF蛋白和TF MP释放。

结论

nLDL和agLDL均可上调VSMC-TF表达。然而,只有agLDL与低密度脂蛋白受体相关蛋白结合才会诱导人VSMC产生细胞TF促凝血活性和TF释放。

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