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Distribution of CD147 During Enteropathogenic Escherichia coli Escherichia coli and Salmonella enterica Salmonella enterica Serovar Typhimurium Infections

机译:CD147在肠致原肠道大肠杆菌大肠杆菌和沙门氏菌肠道沙门氏菌肠道肠道毒蕈中的分布

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ABSTRACT Enteropathogenic Escherichia coli (EPEC) and Salmonella enterica serovar Typhimurium ( S . Typhimurium) are highly infectious gastrointestinal human pathogens. These microbes inject bacterial‐derived effector proteins directly into the host cell cytosol as part of their disease processes. A common host subcellular target of these pathogens is the actin cytoskeleton, which is commandeered by the bacteria and is used during their attachment onto (EPEC) or invasion into ( S . Typhimurium) the host cells. We previously demonstrated that the host enzyme cyclophilin A (CypA) is recruited to the actin‐rich regions of EPEC pedestals and S . Typhimurium membrane ruffles. To further expand the growing catalogue of host proteins usurped by actin‐hijacking bacteria, we examined the host plasma membrane protein and cognate receptor of CypA, CD147, during EPEC and S . Typhimurium infections. Here, we show that CD147 is enriched at the basolateral regions of pedestals but, unlike CypA, it is absent from their actin‐rich core. We show that the CD147 recruitment to these areas requires EPEC pedestal formation and not solely bacteria‐host cell contact. Additionally, we demonstrate that the depletion of CD147 by siRNA does not alter the formation of pedestals. Finally, we show that CD147 is also a component of actin‐rich membrane ruffles generated during S . Typhimurium invasion of host cells. Collectively, our findings establish CD147 as another host component present at dynamic actin‐rich structures formed during bacterial infections. Anat Rec, 302:2224–2232, 2019. ? 2019 American Association for Anatomy
机译:摘要肠疗法大肠杆菌(EPEC)和沙门氏菌肠道血吸虫伤寒伤寒毒蕈这些微生物将细菌衍生的效应蛋白直接注入宿主细胞胞嘧啶,作为其疾病方法的一部分。这些病原体的常见宿主亚细胞靶标是肌动蛋白的细胞骨架,其被细菌征服,并且在其附着在(EPEC)或侵入到(s.Typhimurium)宿主细胞期间使用。我们以前证明宿主酶环旋蛋白A(CYPA)被募集到EPEC基座的致动蛋白的地区。刺血管膜褶边。为了进一步扩大由肌动蛋白劫持细菌篡夺的宿主蛋白的不断增长目录,我们在EPEC和S期间检查了Cypa,CD147的宿主血浆膜蛋白和同源受体。伤寒蕈下感染。在这里,我们表明CD147在基座的基石区域富集,但与CYPA不同,它不存在于富有的富含CYPA的核心。我们表明CD147对这些领域的招募需要EPEC基座形成,并不仅仅是细菌 - 宿主细胞接触。另外,我们证明siRNA的CD147的耗尽不会改变基座的形成。最后,我们表明CD147也是在S中产生的富含富含蛋白的膜荷丝的组成部分。刺鼠宿主细胞的侵袭。集体,我们的研究结果将CD147建立为在细菌感染中形成的动态肌动蛋白的结构中存在的另一个宿主成分。 ANAT REC,302:2224-2232,2019。? 2019年美国解剖学协会

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