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引用本文的文献

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Mitochondrial Dysfunction in Bacterial Infections.细菌感染中的线粒体功能障碍
Pathogens. 2023 Aug 1;12(8):1005. doi: 10.3390/pathogens12081005.
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Mitochondrial recovery by the UPR: Insights from C. elegans.线粒体通过 UPR 恢复:来自秀丽隐杆线虫的见解。
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Mitochondria as novel mediators linking gut microbiota to atherosclerosis that is ameliorated by herbal medicine: A review.线粒体作为肠道微生物群与动脉粥样硬化之间联系的新型介质,而草药可改善这种联系:综述。
Front Pharmacol. 2023 Jan 17;14:1082817. doi: 10.3389/fphar.2023.1082817. eCollection 2023.
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The mitochondrial UPR regulator ATF5 promotes intestinal barrier function via control of the satiety response.线粒体 UPR 调节剂 ATF5 通过控制饱腹感反应促进肠道屏障功能。
Cell Rep. 2022 Dec 13;41(11):111789. doi: 10.1016/j.celrep.2022.111789.
6
Enteropathogenic regulates host-cell mitochondrial morphology.肠致病性细菌调控宿主细胞线粒体形态。
Gut Microbes. 2022 Jan-Dec;14(1):2143224. doi: 10.1080/19490976.2022.2143224.

在进攻和防守中:靶向致病攻击中的线粒体恢复计划。

On the offense and defense: mitochondrial recovery programs amidst targeted pathogenic assault.

机构信息

Department of Biology, University of Texas Arlington, TX, USA.

出版信息

FEBS J. 2022 Nov;289(22):7014-7037. doi: 10.1111/febs.16126. Epub 2021 Jul 30.

DOI:10.1111/febs.16126
PMID:34270874
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9192128/
Abstract

Bacterial pathogens employ a variety of tactics to persist in their host and promote infection. Pathogens often target host organelles in order to benefit their survival, either through manipulation or subversion of their function. Mitochondria are regularly targeted by bacterial pathogens owing to their diverse cellular roles, including energy production and regulation of programmed cell death. However, disruption of normal mitochondrial function during infection can be detrimental to cell viability because of their essential nature. In response, cells use multiple quality control programs to mitigate mitochondrial dysfunction and promote recovery. In this review, we will provide an overview of mitochondrial recovery programs including mitochondrial dynamics, the mitochondrial unfolded protein response (UPR ), and mitophagy. We will then discuss the various approaches used by bacterial pathogens to target mitochondria, which result in mitochondrial dysfunction. Lastly, we will discuss how cells leverage mitochondrial recovery programs beyond their role in organelle repair, to promote host defense against pathogen infection.

摘要

细菌病原体采用多种策略在宿主体内存活并促进感染。病原体通常针对宿主细胞器,以通过操纵或颠覆其功能来获益其生存。由于线粒体具有多种细胞作用,包括能量产生和程序性细胞死亡的调节,因此经常成为细菌病原体的靶标。然而,由于其本质上的重要性,感染过程中正常线粒体功能的破坏可能对细胞活力有害。作为回应,细胞使用多种质量控制程序来减轻线粒体功能障碍并促进恢复。在这篇综述中,我们将概述线粒体恢复程序,包括线粒体动力学、线粒体未折叠蛋白反应 (UPR) 和线粒体自噬。然后,我们将讨论细菌病原体用于靶向线粒体的各种方法,这些方法导致线粒体功能障碍。最后,我们将讨论细胞如何利用线粒体恢复程序超越其在细胞器修复中的作用,以促进宿主防御病原体感染。