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过氧化氢对于支气管上皮细胞肺炎球菌感染中NLRP3炎性小体介导的IL-1β产生和细胞死亡至关重要。

Hydrogen Peroxide Is Crucial for NLRP3 Inflammasome-Mediated IL-1β Production and Cell Death in Pneumococcal Infections of Bronchial Epithelial Cells.

作者信息

Surabhi Surabhi, Jachmann Lana H, Shumba Patience, Burchhardt Gerhard, Hammerschmidt Sven, Siemens Nikolai

机构信息

Department of Molecular Genetics and Infection Biology, Interfaculty Institute for Genetics and Functional Genomics, Center for Functional Genomics of Microbes, University of Greifswald, Greifswald, Germany.

出版信息

J Innate Immun. 2022;14(3):192-206. doi: 10.1159/000517855. Epub 2021 Aug 6.

Abstract

Epithelial cells play a crucial role in detection of the pathogens as well as in initiation of the host immune response. Streptococcus pneumoniae (pneumococcus) is a typical colonizer of the human nasopharynx, which can disseminate to the lower respiratory tract and subsequently cause severe invasive diseases such as pneumonia, sepsis, and meningitis. Hydrogen peroxide (H2O2) is produced by pneumococci as a product of the pyruvate oxidase SpxB. However, its role as a virulence determinant in pneumococcal infections of the lower respiratory tract is not well understood. In this study, we investigated the role of pneumococcal-derived H2O2 in initiating epithelial cell death by analyzing the interplay between 2 key cell death pathways, namely, apoptosis and pyroptosis. We demonstrate that H2O2 primes as well as activates the NLRP3 inflammasome and thereby mediates IL-1β production and release. Furthermore, we show that pneumococcal H2O2 causes cell death via the activation of both apoptotic as well as pyroptotic pathways which are mediated by the activation of caspase-3/7 and caspase-1, respectively. However, H2O2-mediated IL-1β release itself occurs mainly via apoptosis.

摘要

上皮细胞在病原体检测以及宿主免疫反应的启动中发挥着关键作用。肺炎链球菌(肺炎球菌)是人类鼻咽部的典型定植菌,可扩散至下呼吸道,随后引发严重的侵袭性疾病,如肺炎、败血症和脑膜炎。过氧化氢(H2O2)由肺炎球菌作为丙酮酸氧化酶SpxB的产物产生。然而,其在下呼吸道肺炎球菌感染中作为毒力决定因素的作用尚未得到充分了解。在本研究中,我们通过分析两种关键细胞死亡途径(即凋亡和焦亡)之间的相互作用,研究了肺炎球菌衍生的H2O2在引发上皮细胞死亡中的作用。我们证明H2O2引发并激活NLRP3炎性小体,从而介导IL-1β的产生和释放。此外,我们表明肺炎球菌H2O2通过分别由caspase-3/7和caspase-1激活介导的凋亡和焦亡途径的激活导致细胞死亡。然而,H2O2介导的IL-1β释放本身主要通过凋亡发生。

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