首页> 美国卫生研究院文献>Cell Death Disease >Gadd45α activity is the principal effector of Shigella mitochondria-dependent epithelial cell death in vitro and ex vivo
【2h】

Gadd45α activity is the principal effector of Shigella mitochondria-dependent epithelial cell death in vitro and ex vivo

机译:Gadd45α活性是体外和离体志贺氏菌线粒体依赖性上皮细胞死亡的主要效应器

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Modulation of death is a pathogen strategy to establish residence and promote survival in host cells and tissues. Shigella spp. are human pathogens that invade colonic mucosa, where they provoke lesions caused by their ability to manipulate the host cell responses. Shigella spp. induce various types of cell death in different cell populations. However, they are equally able to protect host cells from death. Here, we have investigated on the molecular mechanisms and cell effectors governing the balance between survival and death in epithelial cells infected with Shigella. To explore these aspects, we have exploited both, the HeLa cell invasion assay and a novel ex vivo human colon organ culture model of infection that mimics natural conditions of shigellosis. Our results definitely show that Shigella induces a rapid intrinsic apoptosis of infected cells, via mitochondrial depolarization and the ensuing caspase-9 activation. Moreover, for the first time we identify the eukaryotic stress-response factor growth arrest and DNA damage 45α as a key player in the induction of the apoptotic process elicited by Shigella in epithelial cells, revealing an unexplored role of this molecule in the course of infections sustained by invasive pathogens.
机译:死亡的调节是在宿主细胞和组织中建立驻留并促进存活的病原体策略。志贺氏菌属。是侵入结肠粘膜的人类病原体,它们在其中引起由操纵宿主细胞反应的能力引起的损害。志贺氏菌属。在不同的细胞群体中诱导各种类型的细胞死亡。但是,它们同样能够保护宿主细胞免于死亡。在这里,我们研究了控制志贺氏菌感染的上皮细胞生存与死亡之间平衡的分子机制和细胞效应子。为了探索这些方面,我们利用了HeLa细胞侵袭试验和一种新型的模拟结肠志贺菌病自然条件的体外人结肠器官感染模型。我们的研究结果明确表明,志贺氏菌通过线粒体去极化和随后的caspase-9激活,诱导了感染细胞的快速内在凋亡。此外,我们首次将真核生物应激反应因子的生长停滞和DNA损伤45α鉴定为志贺氏菌诱导的上皮细胞凋亡过程的关键参与者,这揭示了该分子在感染过程中的尚未探索的作用。由侵入性病原体维持。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号