Evidence map›Paper›PMID 26496644›Full record

ArticlePloS one2015

An Automated Strategy for Unbiased Morphometric Analyses and Classifications of Growth Cones In Vitro.

Daryan Chitsaz, Daniel Morales, Chris Law, Artur Kania

Abstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

4 authors.

Daryan ChitsazInstitut de recherches cliniques de Montréal, Montréal, Canada.
Daniel MoralesInstitut de recherches cliniques de Montréal, Montréal, Canada; Integrated Program in Neuroscience, McGill University, Montréal, Canada.
Chris LawInstitut de recherches cliniques de Montréal, Montréal, Canada.
Artur KaniaInstitut de recherches cliniques de Montréal, Montréal, Canada; Integrated Program in Neuroscience, McGill University, Montréal, Canada; Division of Experimental Medicine, Department of Anatomy and Cell Biology and Department of Biology, McGill University, Montréal, Canada; Faculté de Médecine, Université de Montréal, Montréal, Canada.

Funding

Canadian Institutes of Health Research MOP-77556Canadian Institutes of Health Research MOP-97758
6 · The paper itself

Abstract

During neural circuit development, attractive or repulsive guidance cue molecules direct growth cones (GCs) to their targets by eliciting cytoskeletal remodeling, which is reflected in their morphology. The experimental power of in vitro neuronal cultures to assay this process and its molecular mechanisms is well established, however, a method to rapidly find and quantify multiple morphological aspects of GCs is lacking. To this end, we have developed a free, easy to use, and fully automated Fiji macro, Conographer, which accurately identifies and measures many morphological parameters of GCs in 2D explant culture images. These measurements are then subjected to principle component analysis and k-means clustering to mathematically classify the GCs as "collapsed" or "extended". The morphological parameters measured for each GC are found to be significantly different between collapsed and extended GCs, and are sufficient to classify GCs as such with the same level of accuracy as human observers. Application of a known collapse-inducing ligand results in significant changes in all parameters, resulting in an increase in 'collapsed' GCs determined by k-means clustering, as expected. Our strategy provides a powerful tool for exploring the relationship between GC morphology and guidance cue signaling, which in particular will greatly facilitate high-throughput studies of the effects of drugs, gene silencing or overexpression, or any other experimental manipulation in the context of an in vitro axon guidance assay.

Indexed as

AlgorithmsAnimalsChick EmbryoGrowth ConesModels, TheoreticalNeurogenesisSignal TransductionSoftware

Identifiers

PMID26496644
PMCPMC4619750

What OpenQuestion holds

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LicenceCC BY
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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.