Evidence map›Paper›PMID 27242509›Full record

ArticleFrontiers in aging neuroscience2016

Isolation and Molecular Profiling of Primary Mouse Retinal Ganglion Cells: Comparison of Phenotypes from Healthy and Glaucomatous Retinas.

Sumana R Chintalapudi, Levon Djenderedjian, Andrew B Stiemke, Jena J Steinle, Monica M Jablonski, Vanessa M Morales-Tirado

Abstract read
In one paragraph

Article in Frontiers in aging neuroscience, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

  1. Article
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  6. Comprehensive single-cell atlas of the mouse retina.bioRxiv : the preprint server for biology · 2024
    Article
  7. Article
  8. Article
  9. Article
  10. Review
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  12. Article
  13. Review
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  16. Article
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  19. Article
  20. [Clinical, morphological and molecular biological characteristics of the aging eye].Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft · 2017
    Review
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.

Sumana R ChintalapudiDepartment of Ophthalmology, The University of Tennessee Health Science Center Memphis, TN, USA.
Levon DjenderedjianDepartment of Ophthalmology, The University of Tennessee Health Science Center Memphis, TN, USA.
Andrew B StiemkeDepartment of Ophthalmology, The University of Tennessee Health Science Center Memphis, TN, USA.
Jena J SteinleDepartment of Anatomy and Cell Biology, Wayne State UniversityDetroit, MI, USA; Department of Ophthalmology, Wayne State UniversityDetroit, MI, USA.
Monica M JablonskiDepartment of Ophthalmology, The University of Tennessee Health Science CenterMemphis, TN, USA; Department of Anatomy and Neurobiology, The University of Tennessee Health Science CenterMemphis, TN, USA; Department of Pharmaceutical Sciences, The University of Tennessee Health Science CenterMemphis, TN, USA.
Vanessa M Morales-TiradoDepartment of Ophthalmology, The University of Tennessee Health Science CenterMemphis, TN, USA; Department of Microbiology, Immunology and Biochemistry, The University of Tennessee Health Science CenterMemphis, TN, USA.

Funding

Genetic Modulators of GlaucomaR01EY021200 · NEI · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI JABLONSKI, MONICA M · 2011 to 2022
$3.2M
Mechanisms of TNFalpha-Induced Insulin Resistance in Retinal CellsR01EY022330 · NEI · WAYNE STATE UNIVERSITY · PI STEINLE, JENA J · 2013 to 2017
$1.5M
NEI NIH HHS R01 EY021200
6 · The paper itself

Abstract

Loss of functional retinal ganglion cells (RGC) is an element of retinal degeneration that is poorly understood. This is in part due to the lack of a reliable and validated protocol for the isolation of primary RGCs. Here we optimize a feasible, reproducible, standardized flow cytometry-based protocol for the isolation and enrichment of homogeneous RGC with the Thy1.2(hi)CD48(neg)CD15(neg)CD57(neg) surface phenotype. A three-step validation process was performed by: (1) genomic profiling of 25-genes associated with retinal cells; (2) intracellular labeling of homogeneous sorted cells for the intracellular RGC-markers SNCG, brain-specific homeobox/POU domain protein 3A (BRN3A), TUJ1, and RNA-binding protein with multiple splicing (RBPMS); and (3) by applying the methodology on RGC from a mouse model with elevated intraocular pressure (IOP) and optic nerve damage. Use of primary RGC cultures will allow for future careful assessment of important cell specific pathways in RGC to provide mechanistic insights into the declining of visual acuity in aged populations and those suffering from retinal neurodegenerative diseases.

Indexed as

flow cytometryglaucomaneurodegenerationretinal cellsretinal ganglion cell

Identifiers

PMID27242509
PMCPMC4870266

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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.