Super-resolution expansion microscopy in plant roots

Super-resolution methods provide far better spatial resolution than the optical diffraction limit of about half the wavelength of light (∼200-300 nm). Nevertheless, they have yet to attain widespread use in plants, largely due to plants' challenging optical properties. Expansion microscopy (ExM) improves effective resolution by isotropically increasing the physical distances between sample structures while preserving relative spatial arrangements and clearing the sample. However, its application to plants has been hindered by the rigid, mechanically cohesive structure of plant tissues. Here, we report on whole-mount ExM of thale cress (Arabidopsis thaliana) root tissues (PlantEx), achieving a 4-fold resolution increase over conventional microscopy. Our results highlight the microtubule cytoskeleton organization and interaction between molecularly defined cellular constituents. Combining PlantEx with stimulated emission depletion microscopy, we increase nanoscale resolution and visualize the complex organization of subcellular organelles from intact tissues by example of the densely packed COPI-coated vesicles associated with the Golgi apparatus and put these into a cellular structural context. Our results show that ExM can be applied to increase effective imaging resolution in Arabidopsis root specimens.

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Publication Details

Journal
The Plant Cell
Published
2025-01-10
DOI
https://doi.org/10.1093/plcell/koaf006
Citations
10
Primary Topic
Advanced Fluorescence Microscopy Techniques
Type
article
Field-Weighted Citation Impact
16.34
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article

Super-resolution expansion microscopy in plant roots

Caroline Kreuzinger, Johann G. Danzl, Sven Truckenbrodt, Jiřı́ Friml et al.
10 citations
The Plant Cell
Advanced Fluorescence Microscopy Techniques
16.34
article

Super-resolution expansion microscopy in plant roots

Caroline Kreuzinger, Johann G. Danzl, Sven Truckenbrodt, Jiřı́ Friml, Eva Benková, Wiebke Jahr, Marek Randuch, Alexander Johnson, Michelle Gallei, Nathalie Agudelo Dueñas, Mojtaba R. Tavakoli, Syamala Inumella, Vitali Vistunou, Jakob Vorlaufer, Christoph Sommer
article en
10 citations

Abstract

Super-resolution methods provide far better spatial resolution than the optical diffraction limit of about half the wavelength of light (∼200-300 nm). Nevertheless, they have yet to attain widespread use in plants, largely due to plants' challenging optical properties. Expansion microscopy (ExM) improves effective resolution by isotropically increasing the physical distances between sample structures while preserving relative spatial arrangements and clearing the sample. However, its application to plants has been hindered by the rigid, mechanically cohesive structure of plant tissues. Here, we report on whole-mount ExM of thale cress (Arabidopsis thaliana) root tissues (PlantEx), achieving a 4-fold resolution increase over conventional microscopy. Our results highlight the microtubule cytoskeleton organization and interaction between molecularly defined cellular constituents. Combining PlantEx with stimulated emission depletion microscopy, we increase nanoscale resolution and visualize the complex organization of subcellular organelles from intact tissues by example of the densely packed COPI-coated vesicles associated with the Golgi apparatus and put these into a cellular structural context. Our results show that ExM can be applied to increase effective imaging resolution in Arabidopsis root specimens.

The Plant CellVol. 37(4)
Institute of Science and Technology Austria (AT)
Openalex Percentile: Top 1%
Advanced Fluorescence Microscopy Techniques
16.34
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