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Study on induction of apoptosis on HeLa and Vero cells by recombinant shiga toxin and its subunits

机译:重组志贺毒素及其亚基诱导HeLa和Vero细胞凋亡的研究

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摘要

Verotoxin (VT) or shiga toxin (Stx) produced by enterohemorrhagic Escherichia coli (EHEC) and Shigella dysenteriae is AB5 holotoxin with potent protein synthesis inhibitor. VT can induce both apoptosis and necrosis depending on the cell type, it has been shown that VT-induced apoptosis and cytotoxicity are distinct processes, and the A subunit can be necessary for apoptosis. In other words, the precise role of each subunit in apoptosis signaling has yet to be established. In this study, induction of apoptosis has been examined by using both recombinant A and B subunits, and recombinant Stx (rStx) with different doses in HeLa and Vero cells. For this purpose, the polymyxin B extract of constructs expressing A, B and AB5 recombinant proteins was used. Therefore, amounts greater than normally reported were used to induce desire effects on cell lines. The apoptotic effect of A and B subunits appear at higher doses than that of rStx. The highest apoptotic effect was observed for rStx at low concentration, compared to A and B subunits. A or B subunits separately cannot induce the signaling pathway stimulated by holotoxin though A subunit, does induce laddering pattern similar to holotoxin. We concluded that both subunits are important in complete death signaling pathway. Since different concentration of A and B subunits and rStx was required in different assay, therefore, it could be emphasized that cell death or even apoptosis caused by either of the subunits or holotoxin depends on sensitivity or specificity of the assay and cell types used.
机译:肠出血性大肠杆菌(EHEC)和痢疾志贺氏菌产生的Verotoxin(VT)或志贺毒素(Stx)是具有有效蛋白质合成抑制剂的AB5全毒素。 VT可以根据细胞类型诱导凋亡和坏死,已经表明VT诱导的凋亡和细胞毒性是不同的过程,并且A亚基可能是凋亡所必需的。换句话说,尚未确定每个亚基在凋亡信号传导中的确切作用。在这项研究中,已经通过在HeLa和Vero细胞中使用重组A和B亚基以及不同剂量的重组Stx(rStx)来检查凋亡的诱导。为此目的,使用表达A,B和AB5重组蛋白的构建体的多粘菌素B提取物。因此,使用比正常报道更大的量来诱导对细胞系的期望作用。 A和B亚单位的凋亡作用出现在比rStx更高的剂量下。与A和B亚单位相比,低浓度的rStx具有最高的凋亡效应。尽管A或B亚基确实会诱导类似于Holotoxin的阶梯模式,但A或B亚基不能分别诱导由全毒素刺激的信号通路。我们得出的结论是,两个亚基在完整的死亡信号传导途径中都很重要。由于在不同的测定中需要不同浓度的A和B亚基和rStx,因此,可以强调的是,由亚基或全毒素引起的细胞死亡甚至细胞凋亡取决于测定的灵敏度或特异性以及所用的细胞类型。

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