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Shiga Toxins as Multi-Functional Proteins: Induction of Host Cellular Stress Responses Role in Pathogenesis and Therapeutic Applications

机译:志贺毒素作为多功能蛋白:诱导宿主细胞应激反应在发病机理和治疗应用中的作用

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摘要

Shiga toxins (Stxs) produced by Shiga toxin-producing bacteria Shigella dysenteriae serotype 1 and select serotypes of Escherichia coli are primary virulence factors in the pathogenesis of hemorrhagic colitis progressing to potentially fatal systemic complications, such as hemolytic uremic syndrome and central nervous system abnormalities. Current therapeutic options to treat patients infected with toxin-producing bacteria are limited. The structures of Stxs, toxin-receptor binding, intracellular transport and the mode of action of the toxins have been well defined. However, in the last decade, numerous studies have demonstrated that in addition to being potent protein synthesis inhibitors, Stxs are also multifunctional proteins capable of activating multiple cell stress signaling pathways, which may result in apoptosis, autophagy or activation of the innate immune response. Here, we briefly present the current understanding of Stx-activated signaling pathways and provide a concise review of therapeutic applications to target tumors by engineering the toxins.
机译:产志贺毒素的细菌痢疾志贺氏菌血清型1和选择的血清型大肠杆菌产生的志贺毒素(Stxs)是出血性结肠炎病情发展为可能致命的系统性并发症(如溶血性尿毒症和中枢神经系统异常)的主要致病因素。目前用于治疗被产毒素细菌感染的患者的治疗选择是有限的。 Stxs的结构,毒素受体结合,细胞内转运和毒素的作用方式已得到很好的定义。然而,在过去的十年中,大量研究表明,Stxs除了是有效的蛋白质合成抑制剂外,还是能够激活多种细胞应激信号通路的多功能蛋白,可能导致细胞凋亡,自噬或激活先天性免疫应答。在这里,我们简要介绍了Stx激活信号通路的当前理解,并提供了通过工程化毒素靶向肿瘤的治疗应用的简明综述。

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