首页> 美国卫生研究院文献>Infection and Immunity >Novel Subtilase Cytotoxin Produced by Shiga-Toxigenic Escherichia coli Induces Apoptosis in Vero Cells via Mitochondrial Membrane Damage
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Novel Subtilase Cytotoxin Produced by Shiga-Toxigenic Escherichia coli Induces Apoptosis in Vero Cells via Mitochondrial Membrane Damage

机译:志贺毒素大肠杆菌产生的新型枯草蛋白酶细胞毒素通过线粒体膜损伤诱导Vero细胞凋亡。

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摘要

Subtilase cytotoxin (SubAB) is an AB5 cytotoxin produced by some strains of Shiga-toxigenic Escherichia coli. The A subunit is a subtilase-like serine protease and cleaves an endoplasmic reticulum chaperone, BiP, leading to transient inhibition of protein synthesis and cell cycle arrest at G1 phase. Here we show that SubAB, but not the catalytically inactive mutant SubAB(S272A), induced apoptosis in Vero cells, as detected by DNA fragmentation and annexin V binding. SubAB induced activation of caspase-3, -7, and -8. Caspase-3 appeared earlier than caspase-8, and by use of specific caspase inhibitors, it was determined that caspase-3 may be upstream of caspase-8. A general caspase inhibitor blocked SubAB-induced apoptosis, detected by annexin V binding. SubAB also stimulated cytochrome c release from mitochondria, which was not suppressed by caspase inhibitors. In HeLa cells, Apaf-1 small interfering RNA inhibited caspase-3 activation, suggesting that cytochrome c might form an apoptosome, leading to activation of caspase-3. These data suggested that SubAB induced caspase-dependent apoptosis in Vero cells through mitochondrial membrane damage.
机译:枯草杆菌蛋白酶细胞毒素(SubAB)是由某些产志贺毒素的大肠杆菌产生的AB5细胞毒素。 A亚基是一种枯草蛋白酶样丝氨酸蛋白酶,可切割内质网伴侣蛋白BiP,从而导致蛋白质合成的短暂抑制和细胞周期阻滞在G1期。在这里,我们显示SubAB,而不是催化失活的突变体SubAB(S272A),可诱导Vero细胞凋亡,如DNA片段化和膜联蛋白V结合所检测。 SubAB诱导caspase-3,-7和-8的激活。 Caspase-3的出现要早于caspase-8,并且通过使用特定的caspase抑制剂,可以确定caspase-3可能在caspase-8的上游。普通的半胱天冬酶抑制剂阻断了膜联蛋白V结合检测到的SubAB诱导的凋亡。 SubAB还刺激线粒体释放细胞色素c,而caspase抑制剂并未抑制这种释放。在HeLa细胞中,Apaf-1小干扰RNA抑制了caspase-3的激活,这表明细胞色素c可能形成凋亡小体,导致caspase-3的激活。这些数据表明,SubAB通过线粒体膜损伤在Vero细胞中诱导caspase依赖性凋亡。

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