Evidence map›Paper›PMID 28943757›Full record

ArticleCell health and cytoskeleton2014

Classification of axonal subtypes based on cytoskeletal components.

Ye Z Spector, Qi Zhao, Xiaopeng Zhao, William J Feuer, Portia Lynn Maravich, Xiang-Run Huang

Open access · diamondAbstract read
In one paragraph

Article in Cell health and cytoskeleton, 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
0.1field-weighted citation impact, top 47% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

6 authors at 2 institutions in 2 countries.

Ye Z SpectorDepartment of Biomedical Engineering, College of Engineering, University of Miami, Miami, FL, USA.
Qi ZhaoDepartment of Ophthalmology, The Second Affiliated Hospital of Dalian Medical University, Dalian, Liaoning, People's Republic of China.
Xiaopeng ZhaoDepartment of Ophthalmology, Bascom Palmer Eye Institute, University of Miami, Leonard M Miller School of Medicine, Miami, FL, USA.
William J FeuerDepartment of Ophthalmology, Bascom Palmer Eye Institute, University of Miami, Leonard M Miller School of Medicine, Miami, FL, USA.
Portia Lynn MaravichDepartment of Ophthalmology, Bascom Palmer Eye Institute, University of Miami, Leonard M Miller School of Medicine, Miami, FL, USA.
Xiang-Run HuangDepartment of Biomedical Engineering, College of Engineering, University of Miami, Miami, FL, USA.
University of Miami · USSecond Affiliated Hospital of Dalian Medical University · CN

Funding

Shared Equipment ModuleP30EY014801 · NEI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI Dmitry V Ivanov · 2004 to 2026
$12.2M
Retinal Nerve Fiber Layer in Glaucoma: Optical Properties and Damage MechanismsR01EY019084 · NEI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI HUANG, XIANGRUN · 2008 to 2017
$2.5M
NEI NIH HHS P30 EY014801NEI NIH HHS R01 EY019084
6 · The paper itself

Abstract

backgroundRetinal ganglion cells are often classified into different subtypes according to their morphology or physiological functions. The axons of RGCs contain three major cytoskeletal components: actin filaments (F-actin); microtubules; and neurofilaments (NFs). The contents of these components vary among axons. Our objective was to classify axons into subtypes based on the contents of cytoskeletal components and study their distributions across the retina in normal rodent retinas.

methodsWhole-mounted retinas of female Wistar rats were stained with phalloidin to label F-actin, anti-β-tubulin monoclonal antibody to mark microtubules, and antineurofilament antibody to label NFs. A confocal laser scanning microscope was used to provide en face images of retinal nerve fiber bundles with a resolution of 0.24 μm/pixel. Staining intensity profiles across axons were obtained for each cytoskeletal component. Axonal subtypes were then determined from the relative contents, indicated by the staining intensity, of these components. Linear density was used to investigate topographical distribution of each subtype across the retina.

resultsNormal axons could be classified into seven subtypes - FMN, FM, FN, and MN subtypes, (in which at least two or three cytoskeletal components were intensely stained), and F, M, and N subtypes, (in which only one cytoskeletal component was intensely stained within an axon). The FMN subtype was the most abundant subtype. There was no preferential distribution of subtypes around the optic nerve head. However, the densities of the axonal subtypes that contained NFs were found significantly different in the central and peripheral retinal regions. Axonal sizes were subtype-dependent.

conclusionAxons of retinal ganglion cells can be classified into different subtypes, based on the contents of axonal cytoskeletal components. The classified subtypes will provide a new means to study selective damage of axonal ultrastructures in ocular neuropathic diseases.

Indexed as

cytoskeletal componentsF-actinmicrotubulesneurofilamentsretina

Identifiers

PMID28943757
PMCPMC5609711
OpenAlexW1979786844

What OpenQuestion holds

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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.