Evidence map›Paper›PMID 42287515›Full record

ArticleNeuroscience bulletin2026

Vesicle3D: An Integrative Platform for 3D Segmentation and Analysis of Vesicles in Cryo-electron Tomograms.

Zheng-Yu Lv, Zhen-Hang Lu, Shuo Liu, Pengcheng Zhou, Pak-Ming Lau, Guo-Qiang Bi, Chang-Lu Tao

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Article in Neuroscience bulletin, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Zheng-Yu Lv *School of Artificial Intelligence and Data Science, University of Science and Technology of China, Hefei, 230027, China.ORCID http://orcid.org/0009-0001-7420-4319
Zhen-Hang Lu *Center for Integrative Imaging, Hefei National Research Center for Physical Sciences at the Microscale, MOE Key Laboratory for Membraneless Organelles and Cellular Dynamics, School of Life Sciences, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, 230027, China.ORCID http://orcid.org/0009-0004-8376-4360
Shuo Liu *Interdisciplinary Center for Brain Information, the Brain Cognition and Brain Disease Institute, Shenzhen-Hong Kong Institute of Brain Science, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, 518055, China.ORCID http://orcid.org/0009-0006-4406-9773
Pengcheng ZhouInterdisciplinary Center for Brain Information, the Brain Cognition and Brain Disease Institute, Shenzhen-Hong Kong Institute of Brain Science, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, 518055, China.ORCID http://orcid.org/0000-0003-1237-3931
Pak-Ming LauCenter for Integrative Imaging, Hefei National Research Center for Physical Sciences at the Microscale, MOE Key Laboratory for Membraneless Organelles and Cellular Dynamics, School of Life Sciences, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, 230027, China.ORCID http://orcid.org/0000-0001-9026-5501
Guo-Qiang BiSchool of Artificial Intelligence and Data Science, University of Science and Technology of China, Hefei, 230027, China. gqbi@ustc.edu.cn.ORCID http://orcid.org/0000-0001-8735-3818
Chang-Lu TaoCenter for Integrative Imaging, Hefei National Research Center for Physical Sciences at the Microscale, MOE Key Laboratory for Membraneless Organelles and Cellular Dynamics, School of Life Sciences, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, 230027, China. taocl@ustc.edu.cn.ORCID http://orcid.org/0000-0003-0236-7239

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Synaptic vesicles (SVs) are essential components of neurotransmission, and their structure and organization are critical determinants of synaptic function. Cryo-electron tomography (cryo-ET) enables the in situ visualization of SVs in a near-native state. However, their accurate segmentation remains challenging owing to the low signal-to-noise ratio, missing-wedge artifacts in synaptic tomograms, and the inherent morphological heterogeneity of SVs. Herein, we present Vesicle3D, an integrated platform that combines: (1) a vesicle-specific denoising and missing-wedge restoration model; (2) a dual-pathway 3D Res-UNet with prediction fusion; (3) ellipsoid-aware post-processing to preserve authentic vesicle morphology; and (4) an interactive, Napari-based graphical user interface for correction and fine-tuning. This method outperformed existing methods, particularly in the detection of ellipsoidal SVs, and demonstrated robust generalization across diverse datasets, including chemically fixed neurons, isolated synaptosomes, and cryo-FIB lamellae. Furthermore, fine-tuning with approximately 200 annotations enabled rapid adaptation to new datasets. Vesicle3D provides a scalable and versatile framework for the large-scale quantitative analysis of vesicles in cryo-tomograms.

Indexed as

3D segmentationCryo-electron tomographyDeep learningSynaptic vesicle

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.