细胞泰坦:病毒力量与线粒体力量的冲突。

IF 8.3 1区 医学 Q1 VIROLOGY
Théo Defresne, Rodolphe Suspène, Jean-Pierre Vartanian
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引用次数: 0

摘要

线粒体在细胞代谢、能量产生和免疫信号传导中起着至关重要的作用,使其成为病毒操纵的关键靶点。病毒利用线粒体功能增强复制和逃避免疫反应。它们还通过改变裂变/融合平衡和调节线粒体自噬来破坏线粒体动力学,这对线粒体质量控制至关重要。此外,它们重编程线粒体代谢,影响氧化磷酸化和糖酵解等途径,以支持复制。病毒通过抑制或激活线粒体介导的细胞凋亡来调节细胞凋亡,从而延长宿主细胞的存活时间或促进病毒的传播。病毒感染还通过活性氧的产生诱导氧化应激,影响细胞完整性。此外,病毒通过降解线粒体抗病毒信号蛋白并触发线粒体DNA的释放来调节免疫反应,从而操纵线粒体抗病毒免疫。了解这些相互作用为了解病毒发病机制提供了有价值的见解,并提供了治疗机会。靶向线粒体功能障碍和增强抗病毒免疫可以为减轻病毒损伤和增强细胞恢复力提供新的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cellular Titanomachy: Viral Forces Clash with Mitochondrial Power.

Mitochondria play a vital role in cellular metabolism, energy production, and immune signaling, making them key targets for viral manipulation. Viruses exploit mitochondrial functions to enhance replication and evade immune responses. They also disrupt mitochondrial dynamics by altering fission/fusion balance and modulating mitophagy, which is essential for mitochondrial quality control. Additionally, they reprogram mitochondrial metabolism, affecting pathways such as oxidative phosphorylation and glycolysis to support replication. Viruses regulate apoptosis, either inhibiting or activating mitochondria-mediated apoptosis to prolong host cell survival or facilitate viral spread. Viral infections also induce oxidative stress through reactive oxygen species generation, affecting cellular integrity. Furthermore, viruses manipulate mitochondrial antiviral immunity by degrading mitochondrial antiviral signaling protein and triggering the release of mitochondrial DNA, modulating immune responses. Understanding these interactions offers valuable insights into viral pathogenesis and presents therapeutic opportunities. Targeting mitochondrial dysfunction and enhancing antiviral immunity could provide new strategies to mitigate viral damage and enhance cellular resilience.

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来源期刊
CiteScore
19.40
自引率
0.90%
发文量
28
期刊介绍: The Annual Review of Virology serves as a conduit for disseminating thrilling advancements in our comprehension of viruses spanning animals, plants, bacteria, archaea, fungi, and protozoa. Its reviews illuminate novel concepts and trajectories in basic virology, elucidating viral disease mechanisms, exploring virus-host interactions, and scrutinizing cellular and immune responses to virus infection. These reviews underscore the exceptional capacity of viruses as potent probes for investigating cellular function.
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