CryoVesNet: A dedicated framework for synaptic vesicle segmentation in cryo-electron tomograms

Cryo-electron tomography (cryo-ET) has the potential to reveal cell structure down to atomic resolution. Nevertheless, cellular cryo-ET data is highly complex, requiring image segmentation for visualization and quantification of subcellular structures. Due to noise and anisotropic resolution in cryo-ET data, automatic segmentation based on classical computer vision approaches usually does not perform satisfactorily. Communication between neurons relies on neurotransmitter-filled synaptic vesicle (SV) exocytosis. Cryo-ET study of the spatial organization of SVs and their interconnections allows a better understanding of the mechanisms of exocytosis regulation. Accurate SV segmentation is a prerequisite to obtaining a faithful connectivity representation. Hundreds of SVs are present in a synapse, and their manual segmentation is a bottleneck. We addressed this by designing a workflow consisting of a convolutional network followed by post-processing steps. Alongside, we provide an interactive tool for accurately segmenting spherical vesicles. Our pipeline can in principle segment spherical vesicles in any cell type as well as extracellular and in vitro spherical vesicles.

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Publication Details

Journal
The Journal of Cell Biology
Published
2024-09-21
DOI
https://doi.org/10.1083/jcb.202402169
Citations
6
Primary Topic
Advanced Electron Microscopy Techniques and Applications
Type
article
Field-Weighted Citation Impact
3.13

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article

CryoVesNet: A dedicated framework for synaptic vesicle segmentation in cryo-electron tomograms

Julika Radecke, Benoît Zuber, Raphaela Seeger, Jakob B. Sørensen et al.
6 citations
The Journal of Cell Biology
Advanced Electron Microscopy Techniques and Applications
3.13
article

CryoVesNet: A dedicated framework for synaptic vesicle segmentation in cryo-electron tomograms

Julika Radecke, Benoît Zuber, Raphaela Seeger, Jakob B. Sørensen, Guillaume Witz, Amin Khosrozadeh
article en
6 citations

Abstract

Cryo-electron tomography (cryo-ET) has the potential to reveal cell structure down to atomic resolution. Nevertheless, cellular cryo-ET data is highly complex, requiring image segmentation for visualization and quantification of subcellular structures. Due to noise and anisotropic resolution in cryo-ET data, automatic segmentation based on classical computer vision approaches usually does not perform satisfactorily. Communication between neurons relies on neurotransmitter-filled synaptic vesicle (SV) exocytosis. Cryo-ET study of the spatial organization of SVs and their interconnections allows a better understanding of the mechanisms of exocytosis regulation. Accurate SV segmentation is a prerequisite to obtaining a faithful connectivity representation. Hundreds of SVs are present in a synapse, and their manual segmentation is a bottleneck. We addressed this by designing a workflow consisting of a convolutional network followed by post-processing steps. Alongside, we provide an interactive tool for accurately segmenting spherical vesicles. Our pipeline can in principle segment spherical vesicles in any cell type as well as extracellular and in vitro spherical vesicles.

The Journal of Cell BiologyVol. 224(1)
University of Bern (CH), University of Copenhagen (DK), Diamond Light Source (GB)
National Science Foundation, University of Bern, Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
Openalex Percentile: Top 7%
Advanced Electron Microscopy Techniques and Applications
3.13
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CryoVesNet: A dedicated framework for synaptic vesicle segmentation in cryo-electron tomograms — Julika Radecke, Benoît Zuber, et al. · The Journal of Cell Biology (2024) | TGRS Research Map | TGRS