Evidence map›Paper›PMID 32967665›Full record

ArticleBMC biology2020

Deep learning-enabled analysis reveals distinct neuronal phenotypes induced by aging and cold-shock.

Sahand Saberi-Bosari, Kevin B Flores, Adriana San-Miguel

Abstract read
In one paragraph

Article in BMC biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
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

11 citing papers in PubMed.

  1. Functional Analysis of Late-Onset Alzheimer's Disease Risk Genes inbioRxiv : the preprint server for biology · 2026
    Article
  2. Article
  3. HarnessingSensors (Basel, Switzerland) · 2025
    Review
  4. Article
  5. Article
  6. The Primary Cilia are Associated with the Axon Initial Segment in Neurons.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
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

3 authors.

Sahand Saberi-BosariDepartment of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, NC, 27695, USA.
Kevin B FloresDepartment of Mathematics, North Carolina State University, Raleigh, NC, 27695, USA.
Adriana San-MiguelDepartment of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, NC, 27695, USA. asanmiguel@ncsu.edu.ORCID 0000-0003-0172-2163

Funding

Elucidating Synaptic Regulators via High-Throughput Morphology CharacterizationR00AG046911 · NIA · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI SAN MIGUEL, ADRIANA · 2016 to 2018
$984k
A platform for in vivo lifelong tracking of aging genes and lifespan prediction under precise environments in C. elegans.R21AG059099 · NIA · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI FLORES, KEVIN, SAN MIGUEL, ADRIANA · 2019 to 2020
$401k
Division of Integrative Organismal Systems 1838314NIA NIH HHS R00 AG046911NIA NIH HHS R21 AG059099
6 · The paper itself

Abstract

backgroundAccess to quantitative information is crucial to obtain a deeper understanding of biological systems. In addition to being low-throughput, traditional image-based analysis is mostly limited to error-prone qualitative or semi-quantitative assessment of phenotypes, particularly for complex subcellular morphologies. The PVD neuron in Caenorhabditis elegans, which is responsible for harsh touch and thermosensation, undergoes structural degeneration as nematodes age characterized by the appearance of dendritic protrusions. Analysis of these neurodegenerative patterns is labor-intensive and limited to qualitative assessment.

resultsIn this work, we apply deep learning to perform quantitative image-based analysis of complex neurodegeneration patterns exhibited by the PVD neuron in C. elegans. We apply a convolutional neural network algorithm (Mask R-CNN) to identify neurodegenerative subcellular protrusions that appear after cold-shock or as a result of aging. A multiparametric phenotypic profile captures the unique morphological changes induced by each perturbation. We identify that acute cold-shock-induced neurodegeneration is reversible and depends on rearing temperature and, importantly, that aging and cold-shock induce distinct neuronal beading patterns.

conclusionThe results of this work indicate that implementing deep learning for challenging image segmentation of PVD neurodegeneration enables quantitatively tracking subtle morphological changes in an unbiased manner. This analysis revealed that distinct patterns of morphological alteration are induced by aging and cold-shock, suggesting different mechanisms at play. This approach can be used to identify the molecular components involved in orchestrating neurodegeneration and to characterize the effect of other stressors on PVD degeneration.

Indexed as

Deep LearningPhenotypeAgingAnimalsCaenorhabditis elegansCold-Shock ResponseNeuronsAgingC. elegansConvolutional neural networksDeep learningMachine learningNeurodegenerationNeuronal beadingPhenotyping

Identifiers

PMID32967665
PMCPMC7510121

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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.