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无乳链球菌诱导人呼吸道上皮(A549)细胞凋亡过程中涉及的活性氧物质

Reactive oxygen species involved in apoptosis induction of human respiratory epithelial (A549) cells by Streptococcus agalactiae.

作者信息

Ferreira Eduardo da Costa Andréia, Alfredo Moraes João, Silva Santos de Oliveira Jessica, Hanthequeste Bittencourt Dos Santos Michelle, da Silva Santos Gabriela, Barja-Fidalgo Christina, Luiza Mattos-Guaraldi Ana, Emy Nagao Prescilla

机构信息

Laboratory of Molecular Biology and Physiology of Streptococci, Instituto de Biologia Roberto Alcantara Gomes, Rio de Janeiro State University, Rio de Janeiro, Brazil.

Laboratory of Biochemical and Cellular Pharmacology, Instituto de Biologia Roberto Alcantara Gomes, Rio de Janeiro State University, Rio de Janeiro, Brazil.

出版信息

Microbiology (Reading). 2016 Jan;162(1):94-99. doi: 10.1099/mic.0.000202. Epub 2015 Oct 21.

Abstract

Streptococcus agalactiae (Group B Streptococcus; GBS) is an important pathogen and is associated with pneumonia, sepsis and meningitis in neonates and adults. GBS infections induce cytotoxicity of respiratory epithelial cells (A549) with generation of reactive oxygen species (ROS) and loss of mitochondrial membrane potential (ψm). The apoptosis of A549 cells by GBS was dependent on the activation of caspase-3 and caspase-9 with increased pro-apoptotic Bim and Bax molecules and decreased Bcl-2 pro-survival protein. Treatment of infected A549 cells with ROS inhibitors (diphenyleniodonium chloride or apocynin) prevented intracellular ROS production and apoptosis. Consequently, oxidative stress is included among the cellular events leading to apoptosis during GBS human invasive infections.

摘要

无乳链球菌(B族链球菌;GBS)是一种重要的病原体,与新生儿和成人的肺炎、败血症及脑膜炎相关。GBS感染可诱导呼吸道上皮细胞(A549)产生细胞毒性,生成活性氧(ROS)并导致线粒体膜电位(ψm)丧失。GBS诱导A549细胞凋亡依赖于半胱天冬酶-3和半胱天冬酶-9的激活,同时促凋亡分子Bim和Bax增加,抗凋亡蛋白Bcl-2减少。用ROS抑制剂(氯化二苯基碘鎓或夹竹桃麻素)处理受感染的A549细胞可防止细胞内ROS产生及凋亡。因此,氧化应激是GBS侵袭性人类感染过程中导致细胞凋亡的细胞事件之一。

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