Unverified paper record
Root Expansion Microscopy (ROOT-ExM): A streamlined super resolution method for plants
bioRxiv · 21 Feb 2024 · 10.1101/2024.02.21.581184
Abstract
Expansion microscopy (ExM) has revolutionized biological imaging by physically enlarging samples, surpassing the light diffraction limit and enabling nanoscale visualization using standard microscopes. While extensively employed across a wide range of biological samples, its application to plant tissues is sparse. In this work, we present ROOT-ExM, an expansion method suited for stiff and intricate multicellular plant tissues, focusing on the primary root of Arabidopsis thaliana. ROOT-ExM achieves isotropic expansion with a fourfold increase in resolution, enabling super-resolution microscopy comparable to STimulated Emission Depletion (STED) microscopy. Labelling is achieved through immunolocalization, compartment-specific dyes, and native fluorescence preservation, while N-Hydroxysuccinimide (NHS) ester-dye conjugates reveal the ultrastructural context of cells alongside specific labelling. We successfully applied ROOT-ExM to image various cellular structures, including the Golgi apparatus, the endoplasmic reticulum, the cytoskeleton, and wall-embedded structures such as plasmodesmata. When combined with lattice light sheet microscopy (LLSM), ROOT-ExM achieves 3D quantitative analysis of nanoscale cellular process, revealing increased vesicular fusion in close proximity of the cell plate during cell division. Achieving super-resolution fluorescence imaging in plant biology remains a formidable challenge. Our findings underscore that ROOT-ExM provides a remarkable, cost-effective solution to this challenge, paving the way for unprecedented insights into plant cellular subcellular architecture. One sentence summaryROOT-ExM achieves super-resolution expansion microscopy in plants
Plant phenotyping relevance
植物組織向けの超解像イメージング手法そのものを開発し、細胞構造の3D定量解析に応用しており、画像取得法が研究の中心である。
abstractIn this work, we present ROOT-ExM, an expansion method suited for stiff and intricate multicellular plant tissues, focusing on the primary root of Arabidopsis thaliana.
abstractWhen combined with lattice light sheet microscopy (LLSM), ROOT-ExM achieves 3D quantitative analysis of nanoscale cellular process
abstractROOT-ExM provides a remarkable, cost-effective solution to this challenge
Code and data availability
The paper's own distortion-analysis pipeline (Jupyter notebooks using SimpleElastix) is the only paper-specific computational asset, but it is available only upon request. LLSpy and SimpleElastix are generic third-party libraries, not authors' assets, and no public phenotype datasets or images are deposited.
No evidence-backed public reproduction asset is currently recorded.
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