Evidence map›Paper›PMID 11165366›Full record

ArticleBrain research. Molecular brain research2001

Characterization of a transformed rat retinal ganglion cell line.

R R Krishnamoorthy, P Agarwal, G Prasanna, K Vopat, W Lambert, H J Sheedlo, I H Pang, D Shade, R J Wordinger, T Yorio and 2 more

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PubMed Publisher
In one paragraph

Article in Brain research. Molecular brain research, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 133 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
133citing papers in PubMed, 1 pooled it
7.0field-weighted citation impact, top 3% 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

133 citing papers in PubMed, 1 synthesis or guideline pooled it, 318 citations in OpenAlex.

  1. Pooled it
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73 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 2 institutions in 1 country.

R R KrishnamoorthyDepartment of Pathology and Anatomy, UNT Health Science Center, 3500 Camp Bowie Blvd., Fort Worth, TX 76107, USA.
P Agarwal
G Prasanna
K Vopat
W Lambert
H J Sheedlo
I H Pang
D Shade
R J Wordinger
T Yorio
A F Clark
N Agarwal
University of North Texas Health Science Center · USUniversity of North Texas · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The purpose of the present study was to establish a rat retinal ganglion cell line by transformation of rat retinal cells. For this investigation, retinal cells were isolated from postnatal day 1 (PN1) rats and transformed with the psi2 E1A virus. In order to isolate retinal ganglion cells (RGC), single cell clones were chosen at random from the transformed cells. Expression of Thy-1 (a marker for RGC), glial fibrillary acidic protein (GFAP, a positive marker for Muller cells), HPC-1/syntaxin (a marker for amacrine cells), 8A1 (a marker for horizontal and ganglion cells) and neurotrophins was studied using reverse transcriptase-polymerase chain reaction (RT-PCR), immunoblotting and immunocytochemistry. One of the retinal cell clones, designated RGC-5, was positive for Thy-1, Brn-3C, Neuritin, NMDA receptor, GABA-B receptor, and synaptophysin expression and negative for GFAP, HPC-1, and 8A1, suggesting that it represented a putative RGC clone. The results of RT-PCR analysis were confirmed by immunocytochemistry for Thy-1 and GFAP. Upon further characterization by immunoblotting, the RGC-5 clone was positive for Thy-1, negative for GFAP, 8A1 and syntaxin. RGC 5 cells were also positive for the expression of neurotrophins and their cognate receptors. To establish the physiological relevance of RGC-5, the effects of serum/trophic factor deprivation and glutamate toxicity were analyzed to determine if these cells would undergo apoptosis. The protective effects of neurotrophins on RGC-5 after serum deprivation was also investigated. Apoptosis was studied by terminal deoxynucleotidyl transferase-mediated fluoresceinated dUTP nick end labeling (TUNEL). Serum deprivation resulted in apoptosis and supplementation with both BDNF and NT-4 in the growth media, protected the RGC-5 cells from undergoing apoptosis. On differentiation with succinyl concanavalin A (sConA), RGC-5 cells became sensitive to glutamate toxicity, which could be reversed by inclusion of ciplizone (MK801). In conclusion, a transformed rat retinal cell line, RGC-5, has certain characteristics of retinal ganglion cells based on Thy-1 and Brn-3C expression and its sensitivity to glutamate excitotoxicity and neurotrophin withdrawal. These cells may be valuable in understanding of retinal ganglion cell biology and physiology including in vitro manipulations in experimental models of glaucoma.

Indexed as

AnimalsAnimals, NewbornAntibodies, MonoclonalAntigens, SurfaceApoptosisBiomarkersBrain-Derived Neurotrophic FactorCell Culture TechniquesCell DifferentiationCell Line, TransformedCulture Media, Serum-FreeDNA-Binding ProteinsGlaucomaGlial Fibrillary Acidic ProteinGlutamic AcidGPI-Linked ProteinsAntibodies, MonoclonalAntigens, SurfaceBiomarkersBrain-Derived Neurotrophic FactorCulture Media, Serum-FreeDNA-Binding ProteinsGlial Fibrillary Acidic ProteinGlutamic AcidGPI-Linked ProteinsNerve Growth FactorsNerve Tissue ProteinsNeuropeptidesNeuroprotective Agentsneurotrophin 4Nrn1 protein, ratReceptors, GABA-BStx1a protein, ratSynaptophysinSyntaxin 1Thy-1 AntigensTranscription Factor Brn-3Transcription Factor Brn-3CTranscription Factors

Identifiers

PMID11165366
OpenAlexW1604048158

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.