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志贺毒素产志贺氏菌大肠杆菌产生的一种强效AB5毒素——枯草杆菌蛋白酶细胞毒素的组织因子依赖性促凝血活性。

Tissue factor–dependent procoagulant activity of subtilase cytotoxin, a potent AB5 toxin produced by shiga toxigenic Escherichia coli.

作者信息

Wang Hui, Paton James C, Thorpe Cheleste M, Bonder Claudine S, Sun Wai Yan, Paton Adrienne W

机构信息

Research Centre for Infectious Diseases, School of Molecular and Biomedical Science, University of Adelaide, Adelaide, South Australia, Australia.

出版信息

J Infect Dis. 2010 Nov 1;202(9):1415-23. doi: 10.1086/656534.

Abstract

Subtilase cytotoxin (SubAB), produced by certain virulent Shiga toxigenic Escherichia coli strains, causes hemolytic uremic syndrome-like pathology in mice, including extensive microvascular thrombosis. SubAB acts by specifically cleaving the essential endoplasmic reticulum chaperone binding immunoglobulin protein (BiP). BiP has been reported to inhibit the activation of tissue factor (TF), the major initiator of extrinsic coagulation. We hypothesized that the apparent prothrombotic effect of SubAB in vivo may involve the stimulation of TF‐dependent procoagulant activity. TF‐dependent procoagulant activity, TF messenger RNA (mRNA) levels, and BiP cleavage were therefore examined in human macrophage cells and primary human umbilical vein endothelial cells exposed to SubAB. In both types of cells, SubAB significantly increased TF‐dependent procoagulant activity, induced TF mRNA expression, and mediated BiP cleavage. No effects were seen when cells were treated with a nonproteolytic mutant toxin, SubAA272B. Our results suggest that the procoagulant effect of SubAB may be dependent on both the up‐regulation of TF expression and the activation of TF by means of BiP cleavage.

摘要

某些产志贺毒素的致病性大肠杆菌菌株产生的枯草杆菌蛋白酶细胞毒素(SubAB),可在小鼠中引发溶血尿毒综合征样病理变化,包括广泛的微血管血栓形成。SubAB通过特异性切割内质网伴侣结合免疫球蛋白蛋白(BiP)发挥作用。据报道,BiP可抑制组织因子(TF)的激活,而TF是外源性凝血的主要启动因子。我们推测,SubAB在体内明显的促血栓形成作用可能涉及刺激TF依赖性促凝活性。因此,我们检测了暴露于SubAB的人巨噬细胞和原代人脐静脉内皮细胞中的TF依赖性促凝活性、TF信使核糖核酸(mRNA)水平以及BiP切割情况。在这两种类型的细胞中,SubAB均显著增加了TF依赖性促凝活性,诱导了TF mRNA表达,并介导了BiP切割。用非蛋白水解突变毒素SubAA272B处理细胞时未观察到任何影响。我们的结果表明,SubAB的促凝作用可能既依赖于TF表达的上调,也依赖于通过BiP切割对TF的激活。

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