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线粒体-细胞核相互作用:协调线粒体DNA的维持

Mitochondria-Nuclear Crosstalk: Orchestrating mtDNA Maintenance.

作者信息

Darfarin Ghazal, Pluth Janice

机构信息

Department of Health Physics and Diagnostic Sciences, University of Nevada, Las Vegas, Nevada, USA.

出版信息

Environ Mol Mutagen. 2025 Jun;66(5):222-242. doi: 10.1002/em.70013. Epub 2025 May 26.

Abstract

The mitochondria (mt) and nucleus engage in a dynamic bidirectional communication to maintain cellular homeostasis, regulating energy production, stress response, and cell fate. Anterograde signaling directs mt function, while retrograde signaling conveys metabolic and stress-related changes from mt to the nucleus. Central to this crosstalk is mitochondrial DNA (mtDNA), which encodes key oxidative phosphorylation components. MtDNA integrity is preserved through quality control mechanisms, including fusion and fission dynamics, mitophagy, and nuclear-encoded DNA repair. Disruption in these pathways contributes to mt dysfunction, oxidative stress, and genetic instability-hallmarks of aging and diseases. Additionally, redox signaling and NAD+ homeostasis integrate mt and nuclear responses, modulating transcriptional programs that support mt biogenesis and stress adaptation. This review explores the molecular mechanisms coordinating mito-nuclear interactions, emphasizing their role in maintaining mtDNA integrity and cellular equilibrium. Understanding these processes provides insights into how mt dysfunction drives aging and disease, paving the way for targeted therapeutic strategies.

摘要

线粒体(mt)与细胞核进行动态双向通讯以维持细胞内稳态,调节能量产生、应激反应和细胞命运。正向信号传导指导线粒体功能,而逆向信号传导则将与代谢和应激相关的变化从线粒体传递至细胞核。这种相互作用的核心是线粒体DNA(mtDNA),它编码关键的氧化磷酸化成分。线粒体DNA的完整性通过质量控制机制得以维持,包括融合与裂变动态、线粒体自噬以及核编码的DNA修复。这些途径的破坏会导致线粒体功能障碍、氧化应激和基因不稳定,这些都是衰老和疾病的特征。此外,氧化还原信号传导和NAD + 稳态整合了线粒体和细胞核的反应,调节支持线粒体生物合成和应激适应的转录程序。本综述探讨了协调线粒体 - 细胞核相互作用的分子机制,强调了它们在维持线粒体DNA完整性和细胞平衡中的作用。了解这些过程有助于深入了解线粒体功能障碍如何驱动衰老和疾病,为靶向治疗策略铺平道路。

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