Evidence map›Paper›PMID 30296290›Full record

ArticlePloS one2018

Automated classification of synaptic vesicles in electron tomograms of C. elegans using machine learning.

Kristin Verena Kaltdorf, Maria Theiss, Sebastian Matthias Markert, Mei Zhen, Thomas Dandekar, Christian Stigloher, Philip Kollmannsberger

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 42% of its field
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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

Who cites it

5 citing papers in PubMed, 8 citations in OpenAlex.

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4 · The record

Corrections and comments

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 at 2 institutions in 2 countries.

Kristin Verena KaltdorfImaging Core Facility, Biocenter, University of Würzburg, Würzburg, Germany.
Maria TheissDepartment of Bioinformatics, Biocenter, University of Würzburg, Würzburg, Germany.
Sebastian Matthias MarkertImaging Core Facility, Biocenter, University of Würzburg, Würzburg, Germany.
Mei ZhenDepartment of Molecular Genetics, University of Toronto, Toronto, Canada.
Thomas DandekarDepartment of Bioinformatics, Biocenter, University of Würzburg, Würzburg, Germany.ORCID 0000-0003-1886-7625
Christian StigloherImaging Core Facility, Biocenter, University of Würzburg, Würzburg, Germany.ORCID 0000-0001-6941-2669
Philip KollmannsbergerCenter for Computational and Theoretical Biology, University of Würzburg, Würzburg, Germany.ORCID 0000-0002-8049-6186
University of Würzburg · DEUniversity of Toronto · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Synaptic vesicles (SVs) are a key component of neuronal signaling and fulfil different roles depending on their composition. In electron micrograms of neurites, two types of vesicles can be distinguished by morphological criteria, the classical "clear core" vesicles (CCV) and the typically larger "dense core" vesicles (DCV), with differences in electron density due to their diverse cargos. Compared to CCVs, the precise function of DCVs is less defined. DCVs are known to store neuropeptides, which function as neuronal messengers and modulators [1]. In C. elegans, they play a role in locomotion, dauer formation, egg-laying, and mechano- and chemosensation [2]. Another type of DCVs, also referred to as granulated vesicles, are known to transport Bassoon, Piccolo and further constituents of the presynaptic density in the center of the active zone (AZ), and therefore are important for synaptogenesis [3]. To better understand the role of different types of SVs, we present here a new automated approach to classify vesicles. We combine machine learning with an extension of our previously developed vesicle segmentation workflow, the ImageJ macro 3D ART VeSElecT. With that we reliably distinguish CCVs and DCVs in electron tomograms of C. elegans NMJs using image-based features. Analysis of the underlying ground truth data shows an increased fraction of DCVs as well as a higher mean distance between DCVs and AZs in dauer larvae compared to young adult hermaphrodites. Our machine learning based tools are adaptable and can be applied to study properties of different synaptic vesicle pools in electron tomograms of diverse model organisms.

Indexed as

AnimalsAxonsCaenorhabditis elegansMachine LearningNerve Tissue ProteinsNeuromuscular JunctionNeuronsNeuropeptidesProtein TransportSecretory VesiclesSynapsesSynaptic VesiclesNerve Tissue ProteinsNeuropeptides

Identifiers

PMID30296290
PMCPMC6175533
OpenAlexW2952140851

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Registered trials

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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.