Actin in mitochondrial regulation and mechanometabolic crosstalk

IF 6 2区 生物学 Q1 CELL BIOLOGY
Peng Shi , Yuhan Zhang , Congying Wu
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引用次数: 0

Abstract

Mitochondria undergo dynamic adaptations to cellular energy demands, changing morphology and function, through active interactions with other cellular organelles and the cytoskeletons. With advances in light and electron microscopy, actin probes for live-cell imaging, as well as proximity labeling, subtle and transient actin structures associated with mitochondria have been resolved and examined, which opened a new era for the understanding of architectural and mechanical regulation of organelles and metabolism. Here, we first review the recent findings that elucidate the actin–mitochondrion interactions in regulating mitochondrial dynamics (including fission, fusion and trafficking), and cristae architecture. Further, we discuss the functional consequences accompanying these morphological changes, which link cellular metabolism to the cytoskeleton and mechanotransduction through direct or indirect organelle control. Moreover, we summarize the avant-garde techniques for probing mitochondrion-associated actin, including new ways to visualize mitochondria–actin interaction in the cytosol and within the mitochondria, methods to identify the molecular components mediating actin–mitochondria crosstalk, and techniques for reconstructing the 3D ultrastructure of actin–mitochondrion interaction. Finally, we conclude pressing issues in this exciting field, calling for interdisciplinary efforts in examine actin–mitochondrion interactions at micro and macro levels. The dynamics and structural integrity of mitochondria are essential for energy metabolism and signal transduction, while their abnormalities lead to mitochondrial dysfunction and severe disease. This review aims to provide a comprehensive perspective on the emerging roles of the actin cytoskeleton in shaping mitochondrial morphology, structure, and functions, providing new angles to understand mitochondria-related diseases.
肌动蛋白在线粒体调控和机械代谢串扰中的作用
线粒体通过与其他细胞器和细胞骨架的积极相互作用,动态适应细胞的能量需求,改变形态和功能。随着光镜和电镜技术的进步,用于活细胞成像的肌动蛋白探针,以及接近标记,与线粒体相关的细微和瞬态肌动蛋白结构已经被解决和研究,这为理解细胞器和代谢的结构和机械调节开辟了一个新的时代。在这里,我们首先回顾了最近的研究结果,阐明了肌动蛋白-线粒体相互作用在调节线粒体动力学(包括裂变、融合和运输)和嵴结构中的作用。此外,我们还讨论了伴随这些形态学变化的功能后果,这些形态学变化通过直接或间接的细胞器控制将细胞代谢与细胞骨架和机械转导联系起来。此外,我们总结了探测线粒体相关肌动蛋白的前沿技术,包括在细胞质和线粒体内可视化线粒体-肌动蛋白相互作用的新方法,鉴定介导肌动蛋白-线粒体串扰的分子成分的方法,以及重建肌动蛋白-线粒体相互作用的3D超微结构的技术。最后,我们总结了这个令人兴奋的领域的紧迫问题,呼吁在微观和宏观水平上研究肌动蛋白-线粒体相互作用的跨学科努力。线粒体的动力学和结构完整性对于能量代谢和信号转导至关重要,而它们的异常会导致线粒体功能障碍和严重的疾病。本文旨在全面介绍肌动蛋白细胞骨架在线粒体形态、结构和功能形成中的新作用,为了解线粒体相关疾病提供新的视角。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Current Opinion in Cell Biology
Current Opinion in Cell Biology 生物-细胞生物学
CiteScore
14.60
自引率
1.30%
发文量
79
审稿时长
93 days
期刊介绍: Current Opinion in Cell Biology (COCEBI) is a highly respected journal that specializes in publishing authoritative, comprehensive, and systematic reviews in the field of cell biology. The journal's primary aim is to provide a clear and readable synthesis of the latest advances in cell biology, helping specialists stay current with the rapidly evolving field. Expert authors contribute to the journal by annotating and highlighting the most significant papers from the extensive body of research published annually, offering valuable insights and saving time for readers by distilling key findings. COCEBI is part of the Current Opinion and Research (CO+RE) suite of journals, which leverages the legacy of editorial excellence, high impact, and global reach to ensure that the journal is a widely read resource integral to scientists' workflow. It is published by Elsevier, a publisher known for its commitment to excellence in scientific publishing and the communication of reproducible biomedical research aimed at improving human health. The journal's content is designed to be an invaluable resource for a diverse audience, including researchers, lecturers, teachers, professionals, policymakers, and students.
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