Evidence map›Paper›PMID 22490806›Full record

ArticleBMC research notes2012

Enhanced generation of retinal progenitor cells from human retinal pigment epithelial cells induced by amniotic fluid.

Fatemeh Sanie-Jahromi, Hamid Ahmadieh, Zahra-Soheila Soheili, Maliheh Davari, Shima Ghaderi, Mozhgan Rezaei Kanavi, Shahram Samiei, Abdolkhalegh Deezagi, Jalil Pakravesh, Abouzar Bagheri

Open access · goldAbstract read
In one paragraph

Article in BMC research notes, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

11 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Amniotic fluid characteristics and its application in stem cell therapy: A review.International journal of reproductive biomedicine · 2022
    Review
  6. Augmented Expression ofIranian journal of public health · 2022
    Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. 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

10 authors at 4 institutions in 1 country.

Fatemeh Sanie-JahromiNational Institute of Genetic Engineering and Biotechnology, Tehran, Iran. fsanie@yahoo.com
Hamid Ahmadieh
Zahra-Soheila Soheili
Maliheh Davari
Shima Ghaderi
Mozhgan Rezaei Kanavi
Shahram Samiei
Abdolkhalegh Deezagi
Jalil Pakravesh
Abouzar Bagheri
National Institute of Genetic Engineering and Biotechnology · IRShahid Beheshti University of Medical Sciences · IRDay General Hospital · IRIranian Legal Medicine Organization · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRetinal progenitor cells are a convenient source of cell replacement therapy in retinal degenerative disorders. The purpose of this study was to evaluate the expression patterns of the homeobox genes PAX6 and CHX10 (retinal progenitor markers) during treatment of human retinal pigment epithelium (RPE) cells with amniotic fluid (AF), RPE cells harvested from neonatal cadaver globes were cultured in a mixture of DMEM and Ham's F12 supplemented with 10% FBS. At different passages, cells were trypsinized and co-cultured with 30% AF obtained from normal fetuses of 1416 weeks gestational age.

resultsCompared to FBS-treated controls, AF-treated cultures exhibited special morphological changes in culture, including appearance of spheroid colonies, improved initial cell adhesion and ordered cell alignment. Cell proliferation assays indicated a remarkable increase in the proliferation rate of RPE cells cultivated in 30% AF-supplemented medium, compared with those grown in the absence of AF. Immunocytochemical analyses exhibited nuclear localization of retinal progenitor markers at a ratio of 33% and 27% for CHX10 and PAX6, respectively. This indicated a 3-fold increase in retinal progenitor markers in AF-treated cultures compared to FBS-treated controls. Real-time PCR data of retinal progenitor genes (PAX6, CHX10 and VSX-1) confirmed these results and demonstrated AF's capacity for promoting retinal progenitor cell generation.

conclusionTaken together, the results suggest that AF significantly promotes the rate of retinal progenitor cell generation, indicating that AF can be used as an enriched supplement for serum-free media used for the in vitro propagation of human progenitor cells.

Indexed as

Amniotic FluidBiomarkersCell AdhesionCell ProliferationCells, CulturedCell ShapeCulture Media, Serum-FreeEpithelial CellsEye ProteinsGene Expression RegulationGestational AgeHomeodomain ProteinsHumansPaired Box Transcription FactorsPAX6 Transcription FactorReal-Time Polymerase Chain ReactionBiomarkersCulture Media, Serum-FreeEye ProteinsHomeodomain ProteinsPaired Box Transcription FactorsPAX6 protein, humanPAX6 Transcription FactorRepressor ProteinsTranscription FactorsVSX1 protein, humanVSX2 protein, human

Identifiers

PMID22490806
PMCPMC3428660
OpenAlexW2094746054

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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.