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1
Tissue factor–dependent procoagulant activity of subtilase cytotoxin, a potent AB5 toxin produced by shiga toxigenic Escherichia coli.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。
J Infect Dis. 2010 Nov 1;202(9):1415-23. doi: 10.1086/656534.
2
Host response to the subtilase cytotoxin produced by locus of enterocyte effacement-negative Shiga-toxigenic Escherichia coli.肠侵袭性大肠杆菌不产志贺毒素的侵袭相关基因座编码的枯草溶菌素细胞毒素引起的宿主反应。
Microbiol Immunol. 2020 Oct;64(10):657-665. doi: 10.1111/1348-0421.12841. Epub 2020 Sep 29.
3
Uptake of Shiga-toxigenic Escherichia coli SubAB by HeLa cells requires an actin- and lipid raft-dependent pathway.志贺毒素大肠杆菌 SubAB被HeLa细胞摄取需要肌动蛋白和脂筏依赖性途径。
Cell Microbiol. 2014 Oct;16(10):1582-601. doi: 10.1111/cmi.12315. Epub 2014 Jun 17.
4
Differential effects of Escherichia coli subtilase cytotoxin and Shiga toxin 2 on chemokine and proinflammatory cytokine expression in human macrophage, colonic epithelial, and brain microvascular endothelial cell lines.大肠杆菌枯草溶菌素细胞毒素和志贺毒素 2 对人巨噬细胞、结肠上皮和脑微血管内皮细胞系趋化因子和促炎细胞因子表达的差异影响。
Infect Immun. 2014 Sep;82(9):3567-79. doi: 10.1128/IAI.02120-14. Epub 2014 Jun 9.
5
Clathrin-dependent trafficking of subtilase cytotoxin, a novel AB5 toxin that targets the endoplasmic reticulum chaperone BiP.网格蛋白依赖性转运枯草杆菌蛋白酶细胞毒素,一种靶向内质网伴侣BiP的新型AB5毒素。
Cell Microbiol. 2008 Mar;10(3):795-806. doi: 10.1111/j.1462-5822.2007.01085.x. Epub 2007 Nov 27.
6
Novel subtilase cytotoxin produced by Shiga-toxigenic Escherichia coli induces apoptosis in vero cells via mitochondrial membrane damage.产志贺毒素大肠杆菌产生的新型枯草杆菌蛋白酶细胞毒素通过线粒体膜损伤诱导 vero 细胞凋亡。
Infect Immun. 2009 Jul;77(7):2919-24. doi: 10.1128/IAI.01510-08. Epub 2009 Apr 20.
7
Subtilase cytotoxin produced by locus of enterocyte effacement-negative Shiga-toxigenic Escherichia coli induces stress granule formation.由肠细胞脱落阴性产志贺毒素大肠杆菌位点产生的枯草杆菌蛋白酶细胞毒素可诱导应激颗粒形成。
Cell Microbiol. 2016 Jul;18(7):1024-40. doi: 10.1111/cmi.12565. Epub 2016 Feb 21.
8
Escherichia coli subtilase cytotoxin induces apoptosis regulated by host Bcl-2 family proteins Bax/Bak.大肠杆菌枯草溶菌素细胞毒素诱导细胞凋亡受宿主 Bcl-2 家族蛋白 Bax/Bak 调节。
Infect Immun. 2010 Nov;78(11):4691-6. doi: 10.1128/IAI.00801-10. Epub 2010 Aug 16.
9
Systemic effects of Subtilase cytotoxin produced by Escherichia coli O113:H21.大肠杆菌O113:H21产生的枯草杆菌蛋白酶细胞毒素的全身效应。
Toxicon. 2017 Mar 1;127:49-55. doi: 10.1016/j.toxicon.2016.12.014. Epub 2017 Jan 3.
10
Involvement of protein disulfide isomerase in subtilase cytotoxin-induced cell death in HeLa cells.蛋白二硫键异构酶参与枯草溶菌素细胞毒素诱导的 HeLa 细胞死亡。
Biochem Biophys Res Commun. 2020 May 14;525(4):1068-1073. doi: 10.1016/j.bbrc.2020.03.008. Epub 2020 Mar 14.

引用本文的文献

1
Combined Action of Shiga Toxin Type 2 and Subtilase Cytotoxin in the Pathogenesis of Hemolytic Uremic Syndrome.志贺毒素 2 型与枯草溶菌素细胞毒素在溶血性尿毒综合征发病机制中的共同作用。
Toxins (Basel). 2021 Jul 29;13(8):536. doi: 10.3390/toxins13080536.
2
Subtilase cytotoxin produced by locus of enterocyte effacement-negative Shiga-toxigenic Escherichia coli induces stress granule formation.由肠细胞脱落阴性产志贺毒素大肠杆菌位点产生的枯草杆菌蛋白酶细胞毒素可诱导应激颗粒形成。
Cell Microbiol. 2016 Jul;18(7):1024-40. doi: 10.1111/cmi.12565. Epub 2016 Feb 21.
3
Differential effects of Escherichia coli subtilase cytotoxin and Shiga toxin 2 on chemokine and proinflammatory cytokine expression in human macrophage, colonic epithelial, and brain microvascular endothelial cell lines.大肠杆菌枯草溶菌素细胞毒素和志贺毒素 2 对人巨噬细胞、结肠上皮和脑微血管内皮细胞系趋化因子和促炎细胞因子表达的差异影响。
Infect Immun. 2014 Sep;82(9):3567-79. doi: 10.1128/IAI.02120-14. Epub 2014 Jun 9.
4
Action of shiga toxin type-2 and subtilase cytotoxin on human microvascular endothelial cells.志贺毒素 2 型和枯草溶菌素细胞毒素对人微血管内皮细胞的作用。
PLoS One. 2013 Jul 30;8(7):e70431. doi: 10.1371/journal.pone.0070431. Print 2013.
5
Facing glycosphingolipid-Shiga toxin interaction: dire straits for endothelial cells of the human vasculature.面对糖鞘脂类与志贺毒素的相互作用:人血管内皮细胞的困境。
Cell Mol Life Sci. 2013 Feb;70(3):425-57. doi: 10.1007/s00018-012-1060-z. Epub 2012 Jul 6.
6
In Vivo leukocyte changes induced by Escherichia coli subtilase cytotoxin.大肠杆菌枯草溶菌素细胞毒素诱导的体内白细胞变化。
Infect Immun. 2011 Apr;79(4):1671-9. doi: 10.1128/IAI.01204-10. Epub 2011 Jan 31.

本文引用的文献

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The coagulant response in sepsis and inflammation.脓毒症和炎症中的凝血反应。
Hamostaseologie. 2010 Jan;30(1):10-2, 14-6.
2
Upregulation of monocyte tissue factor activity is significantly associated with low-grade chronic inflammation and insulin resistance in patients with metabolic syndrome.单核细胞组织因子活性的上调与代谢综合征患者的低水平慢性炎症和胰岛素抵抗显著相关。
Circ J. 2010 Mar;74(3):572-7. doi: 10.1253/circj.cj-09-0835. Epub 2010 Jan 26.
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Role of tissue factor in cancer.组织因子在癌症中的作用。
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4
Activation of the Akt-NF-kappaB pathway by subtilase cytotoxin through the ATF6 branch of the unfolded protein response.枯草杆菌蛋白酶细胞毒素通过未折叠蛋白反应的ATF6分支激活Akt-NF-κB信号通路。
J Immunol. 2009 Jul 15;183(2):1480-7. doi: 10.4049/jimmunol.0900017. Epub 2009 Jun 26.
5
Subtilase cytotoxin activates PERK, IRE1 and ATF6 endoplasmic reticulum stress-signalling pathways.枯草杆菌蛋白酶细胞毒素激活PERK、IRE1和ATF6内质网应激信号通路。
Cell Microbiol. 2008 Sep;10(9):1775-86. doi: 10.1111/j.1462-5822.2008.01164.x. Epub 2008 Apr 21.
6
Clathrin-dependent trafficking of subtilase cytotoxin, a novel AB5 toxin that targets the endoplasmic reticulum chaperone BiP.网格蛋白依赖性转运枯草杆菌蛋白酶细胞毒素,一种靶向内质网伴侣BiP的新型AB5毒素。
Cell Microbiol. 2008 Mar;10(3):795-806. doi: 10.1111/j.1462-5822.2007.01085.x. Epub 2007 Nov 27.
7
Pathologic changes in mice induced by subtilase cytotoxin, a potent new Escherichia coli AB5 toxin that targets the endoplasmic reticulum.枯草杆菌蛋白酶细胞毒素(一种靶向内质网的强效新型大肠杆菌AB5毒素)诱导的小鼠病理变化。
J Infect Dis. 2007 Oct 1;196(7):1093-101. doi: 10.1086/521364. Epub 2007 Aug 22.
8
AB5 subtilase cytotoxin inactivates the endoplasmic reticulum chaperone BiP.AB5 枯草杆菌蛋白酶细胞毒素可使内质网伴侣蛋白 BiP 失活。
Nature. 2006 Oct 5;443(7111):548-52. doi: 10.1038/nature05124.
9
Getting a GRP on tissue factor activation.获取关于组织因子激活的总体反应潜能(GRP)。
Arterioscler Thromb Vasc Biol. 2005 Aug;25(8):1529-31. doi: 10.1161/01.ATV.0000177041.47444.e2.
10
Protective immunization of mice with an active-site mutant of subtilase cytotoxin of Shiga toxin-producing Escherichia coli.用产志贺毒素大肠杆菌枯草杆菌蛋白酶细胞毒素的活性位点突变体对小鼠进行保护性免疫接种。
Infect Immun. 2005 Jul;73(7):4432-6. doi: 10.1128/IAI.73.7.4432-4436.2005.

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.

DOI:10.1086/656534
PMID:20874089
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2949535/
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。