Department of Microbial & Molecular Pathogenesis, College of Medicine, Texas A&M University System Health Science Center, 407 Reynolds Medical Building, College Station, TX 77843-1114, USA.
Future Microbiol. 2010 Mar;5(3):431-53. doi: 10.2217/fmb.10.4.
Shiga toxins comprise a family of structurally and functionally related protein toxins expressed by Shigella dysenteriae serotype 1 and multiple serotypes of Escherichia coli. While the capacity of Shiga toxins to inhibit protein synthesis by catalytic inactivation of eukaryotic ribosomes has been well described, it is also apparent that Shiga toxins trigger apoptosis in many cell types. This review presents evidence that Shiga toxins induce apoptosis of epithelial, endothelial, leukocytic, lymphoid and neuronal cells. Apoptotic signaling pathways activated by the toxins are reviewed with an emphasis on signaling mechanisms that are shared among different cell types. Data suggesting that Shiga toxins induce apoptosis through the endoplasmic reticulum stress response and clinical evidence demonstrating apoptosis in humans infected with Shiga toxin-producing bacteria are briefly discussed. The potential for use of Shiga toxins to induce apoptosis in cancer cells is briefly reviewed.
志贺毒素由志贺氏痢疾杆菌血清型 1 和多种大肠杆菌血清型表达的一组结构和功能相关的蛋白毒素组成。虽然志贺毒素通过催化失活真核核糖体来抑制蛋白质合成的能力已得到充分描述,但显然志贺毒素也能引发许多细胞类型的细胞凋亡。这篇综述提供了证据表明志贺毒素诱导上皮细胞、内皮细胞、白细胞、淋巴样细胞和神经元细胞凋亡。本文综述了毒素激活的凋亡信号通路,并重点讨论了不同细胞类型共有的信号机制。简要讨论了提示志贺毒素通过内质网应激反应诱导细胞凋亡的证据以及临床证据证明感染产志贺毒素细菌的人类发生细胞凋亡。简要回顾了使用志贺毒素诱导癌细胞凋亡的可能性。