Evidence map›Paper›PMID 24680908›Full record

ArticleJournal of neuroscience methods2014

Semi-automatic quantification of neurite fasciculation in high-density neurite images by the neurite directional distribution analysis (NDDA).

Amy M Hopkins, Brandon Wheeler, Cristian Staii, David L Kaplan, Timothy J Atherton

Abstract read
In one paragraph

Article in Journal of neuroscience methods, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Amy M HopkinsDepartment of Biomedical Engineering, Tufts University Science & Technology Center, 4 Colby Street, Medford, MA 02155, USA. Electronic address: Amy.Hopkins@Tufts.edu.
Brandon WheelerDepartment of Biomedical Engineering, Tufts University Science & Technology Center, 4 Colby Street, Medford, MA 02155, USA. Electronic address: Brandon.Wheeler@Tufts.edu.
Cristian StaiiDepartment of Physics and Astronomy, and Center for Nanoscopic Physics, Tufts University Science & Technology Center, 4 Colby Street, Medford, MA 02155, USA. Electronic address: Cristian.Staii@Tufts.edu.
David L KaplanDepartment of Biomedical Engineering, Tufts University Science & Technology Center, 4 Colby Street, Medford, MA 02155, USA. Electronic address: David.Kaplan@Tufts.edu.
Timothy J AthertonDepartment of Physics and Astronomy, and Center for Nanoscopic Physics, Tufts University Science & Technology Center, 4 Colby Street, Medford, MA 02155, USA. Electronic address: Timothy.Atherton@Tufts.edu.

Funding

Translational Bioreactors - Engineering Complex TissuesP41EB002520 · NIBIB · TUFTS UNIVERSITY MEDFORD · PI KAPLAN, DAVID L. · 2004 to 2018
$16.7M
Multifunctional Tropoelastin-Silk Biomaterial SystemsR01EB014283 · NIBIB · TUFTS UNIVERSITY MEDFORD · PI KAPLAN, DAVID L. · 2012 to 2015
$1.2M
NIBIB NIH HHS P41 EB002520NIBIB NIH HHS R01 EB014283
6 · The paper itself

Abstract

backgroundBundling of neurite extensions occur during nerve development and regeneration. Understanding the factors that drive neurite bundling is important for designing biomaterials for nerve regeneration toward the innervation target and preventing nociceptive collateral sprouting. High-density neuron cultures including dorsal root ganglia explants are employed for in vitro screening of biomaterials designed to control directional outgrowth. Although some semi-automated image processing methods exist for quantification of neurite outgrowth, methods to quantify axonal fasciculation in terms of direction of neurite outgrowth are lacking. NEW

methodThis work presents a semi-automated program to analyze micrographs of high-density neurites; the program aims to quantify axonal fasciculation by determining the orientational distribution function of the tangent vectors of the neurites and calculating its Fourier series coefficients ('c' values).

resultsWe found that neurite directional distribution analysis (NDDA) of fasciculated neurites yielded 'c' values of ≥∼0.25 whereas branched outgrowth led to statistically significant lesser values of <∼0.2. The 'c' values correlated directly to the width of neurite bundles and indirectly to the number of branching points. COMPARISON WITH EXISTING

methodsInformation about the directional distribution of outgrowth is lost in simple counting methods or achieved laboriously through manual analysis. The NDDA supplements previous quantitative analyses of axonal bundling using a vector-based approach that captures new information about the directionality of outgrowth.

conclusionThe NDDA is a valuable addition to open source image processing tools available to biomedical researchers offering a robust, precise approach to quantification of imaged features important in tissue development, disease, and repair.

Indexed as

Analysis of VarianceAnimalsCell PolarityCells, CulturedChick EmbryoGanglia, SpinalImage Processing, Computer-AssistedIn Vitro TechniquesNeuritesNeuronsOptical ImagingTubulinTubulinAxonal alignmentAxonal bundlingAxon branchingDorsal root gangliaFasciculationImage processingNeurite quantification methods

Identifiers

PMID24680908
PMCPMC4057284

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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.