Valera-Alberni Miriam, Yao Pallas, Romero-Sanz Silvia, Lanjuin Anne, Mair William B
bioRxiv. 2024 Jul 16:2024.07.16.603730. doi: 10.1101/2024.07.16.603730.
Mitochondria exhibit a close interplay between their structure and function. Understanding this intricate relationship requires advanced imaging techniques that can capture the dynamic nature of mitochondria and their impact on cellular processes. However, much of the work on mitochondrial dynamics has been done in single celled organisms or in vitro cell culture. Here, we introduce novel genetic tools for live imaging of mitochondrial networks in the nematode , addressing a pressing need for advanced techniques in studying organelle dynamics within live intact multicellular organisms. Through a comprehensive analysis, we directly compare our tools with existing methods, demonstrating their advantages for visualizing mitochondrial morphology and contrasting their impact on organismal physiology. We reveal limitations of conventional techniques, while showcasing the utility and versatility of our approaches, including endogenous CRISPR tags and ectopic labeling. By providing a guide for selecting the most suitable tools based on experimental goals, our work advances mitochondrial research in and enhances the strategic integration of diverse imaging modalities for a holistic understanding of organelle dynamics in living organisms.
线粒体的结构与功能之间存在着密切的相互作用。理解这种复杂的关系需要先进的成像技术,这些技术能够捕捉线粒体的动态特性及其对细胞过程的影响。然而,关于线粒体动态变化的许多研究工作是在单细胞生物或体外细胞培养中进行的。在此,我们介绍用于对线虫中线粒体网络进行实时成像的新型遗传工具,满足了在完整的活多细胞生物体内研究细胞器动态变化的先进技术的迫切需求。通过全面分析,我们将我们的工具与现有方法进行了直接比较,展示了它们在可视化线粒体形态方面的优势,并对比了它们对生物体生理学的影响。我们揭示了传统技术的局限性,同时展示了我们方法的实用性和多功能性,包括内源性CRISPR标签和异位标记。通过根据实验目标提供选择最合适工具的指南,我们的工作推动了线虫中线粒体的研究,并加强了多种成像方式的战略整合,以全面了解活生物体中的细胞器动态变化。