Evidence map›Paper›PMID 10824670›Full record

ArticleVisual neuroscience

Differential induction of gene expression by basic fibroblast growth factor and neuroD in cultured retinal pigment epithelial cells.

R T Yan, S Z Wang

Open access · greenAbstract read
In one paragraph

Article in Visual neuroscience. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

18 citing papers in PubMed, 31 citations in OpenAlex.

  1. Augmented Expression ofIranian journal of public health · 2022
    Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Enhanced retinal ganglion cell differentiation by ath5 and NSCL1 coexpression.Investigative ophthalmology & visual science · 2004
    Article
  13. A role of ath5 in inducing neuroD and the photoreceptor pathway.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2004
    Article
  14. Requirement of neuroD for photoreceptor formation in the chick retina.Investigative ophthalmology & visual science · 2004
    Article
  15. BETA2/NeuroD1 null mice: a new model for transcription factor-dependent photoreceptor degeneration.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2003
    Article
  16. neurogenin2 elicits the genesis of retinal neurons from cultures of nonneural cells.Proceedings of the National Academy of Sciences of the United States of America · 2001
    Article
  17. Article
  18. 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

2 authors at 1 institution in 1 country.

R T YanDepartment of Ophthalmology, University of Alabama at Birmingham School of Medicine, USA.
S Z Wang
University of Alabama at Birmingham · US

Funding

MOLECULAR BIOLOGY OF RETINAL DEVELOPMENTR01EY011640 · NEI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI WANG, SHU-ZHEN · 1997 to 2016
$4.1M
NEI NIH HHS EY11640NEI NIH HHS R01 EY011640
6 · The paper itself

Abstract

Embryonic chick retinal pigment epithelial (RPE) cells can undergo transdifferentiation upon appropriate stimulation. For example, basic fibroblast growth factor (bFGF) induces intact RPE tissue younger than embryonic day 4.5 (E4.5) to transdifferentiate into a neural retina. NeuroD, a gene encoding a basic helix-loop-helix transcription factor, triggers de novo production of cells that resemble young photoreceptor cells morphologically and express general neuron markers (HNK-1/N-CAM and MAP2) and a photoreceptor-specific marker (visinin) from cell cultures of dissociated E6 RPE (Yan & Wang, 1998). The present study examined whether bFGF will lead to the same transdifferentiation phenomenon as neuroD when applied to dissociated, cultured E6 RPE cells, and whether interplay exists between the two factors under the culture conditions. Dissociated E6 RPE cells were cultured in the presence or absence of bFGF, and with or without the addition of retrovirus expressing neuroD. Gene expression was analyzed with immunocytochemistry and in situ hybridization. Unlike neuroD, bFGF did not induce the expression of visinin, or HNK-1/N-CAM and MAP2. However, bFGF elicited the expression of RA4 immunogenicity; yet, many of these RA4-positive cells lacked a neuronal morphology. Addition of bFGF to neuroD-expressing cultures did not alter the number of visinin-expressing cells; misexpression of neuroD in bFGF-treated cultures did not change the number of RA4-positive cells, suggesting the absence of interference or synergistic interaction between the two factors. Our data indicated that bFGF and neuroD induced the expression of different genes in cultured RPE cells.

Indexed as

AnimalsBasic Helix-Loop-Helix ProteinsCells, CulturedChick EmbryoEye ProteinsFibroblast Growth Factor 2Gene Expression RegulationHelix-Loop-Helix MotifsImmunohistochemistryIn Situ HybridizationMicrotubule-Associated ProteinsNerve Tissue ProteinsNeural Cell Adhesion MoleculesPigment Epithelium of EyeBasic Helix-Loop-Helix ProteinsEye ProteinsFibroblast Growth Factor 2Microtubule-Associated ProteinsNerve Tissue ProteinsNeural Cell Adhesion MoleculesNeurogenic differentiation factor 1visinin

Identifiers

PMID10824670
PMCPMC1986837
OpenAlexW2140604260

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.