Evidence map›Paper›PMID 21460262›Full record

ArticleInvestigative ophthalmology & visual science2011

Comparison of FRPE and human embryonic stem cell-derived RPE behavior on aged human Bruch's membrane.

Ilene K Sugino, Qian Sun, Jianqiu Wang, Celia F Nunes, Noounanong Cheewatrakoolpong, Aprille Rapista, Adam C Johnson, Christopher Malcuit, Irina Klimanskaya, Robert Lanza and 1 more

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Investigative ophthalmology & visual science, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
7.6field-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

28 citing papers in PubMed, 76 citations in OpenAlex.

  1. Review
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  9. Nanofiber Scaffold-Based Tissue-Engineered Retinal Pigment Epithelium to Treat Degenerative Eye Diseases.Journal of ocular pharmacology and therapeutics : the official journal of the Association for Ocular Pharmacology and Therapeutics · 2016
    Review
  10. Article
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  12. Progressing a human embryonic stem-cell-based regenerative medicine therapy towards the clinic.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2015
    Review
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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

11 authors at 2 institutions in 1 country.

Ilene K SuginoThe Institute of Ophthalmology and Visual Science, New Jersey Medical School, University of Medicine and Dentistry of New Jersey, 90 Bergen Street, Newark, NJ 07101, USA.
Qian Sun
Jianqiu Wang
Celia F Nunes
Noounanong Cheewatrakoolpong
Aprille Rapista
Adam C Johnson
Christopher Malcuit
Irina Klimanskaya
Robert Lanza
Marco A Zarbin
Rutgers New Jersey Medical SchoolAdvanced Cell Technology (United States) · US

Funding

LABORATORY OF DEVELOPMENTAL BIOLOGYR24HD000836 · NICHD · UNIVERSITY OF WASHINGTON · PI Ian Amos Glass · 1995 to 2026
$16.9M
NICHD NIH HHS R24 HD000836NICHD NIH HHS R24HD000836
6 · The paper itself

Abstract

purposeTo compare RPE derived from human embryonic stem cells (hES-RPE) and fetal RPE (fRPE) behavior on human Bruch's membrane (BM) from aged and AMD donors.

methodshES-RPE of 3 degrees of pigmentation and fRPE were cultured on BM explants. Explants were assessed by light, confocal, and scanning electron microscopy. Integrin mRNA levels were determined by real-time polymerase chain reaction studies. Secreted proteins in media were analyzed by multiplex protein analysis after 48-hour exposure at culture day 21.

resultshES-RPE showed impaired initial attachment compared to fRPE; pigmented hES-RPE showed nuclear densities similar to fRPE at day 21. At days 3 and 7, hES-RPE resurfaced BM to a limited degree, showed little proliferation (Ki-67), and partial retention of RPE markers (MITF, cytokeratin, and CRALBP). TUNEL-positive nuclei were abundant at day 3. fRPE exhibited substantial BM resurfacing at day 3 with decreased resurfacing at later times. Most fRPE retained RPE markers. Ki-67-positive nuclei decreased with time in culture. TUNEL staining was variable. Increased integrin mRNA expression did not appear to affect cell survival at day 21. hES-RPE and fRPE protein secretion was similar on equatorial BM except for higher levels of nerve growth factor and thrombospondin-2 (TSP2) by hES-RPE. On submacular BM, fRPE secreted more vascular endothelial growth factor (VEGF), brain-derived neurotrophic factor, and platelet-derived growth factor; hES-RPE secreted more TSP2.

conclusionsAlthough pigmented hES-RPE and fRPE resurfaced aged and AMD BM to a similar, limited degree at day 21, cell behavior at earlier times was markedly dissimilar. Differences in protein secretion may indicate that hES-RPE may not function identically to native RPE after seeding on aged or AMD BM.

Indexed as

AgedAged, 80 and overAgingBruch MembraneCarrier ProteinsCells, CulturedEmbryonic Stem CellsFemaleFetal Stem CellsFluorescent Antibody Technique, IndirectHumansIn Situ Nick-End LabelingIntegrinsKeratinsKi-67 AntigenMacular Degeneration11-cis-retinal-binding proteinCarrier ProteinsIntegrinsKeratinsKi-67 AntigenMicrophthalmia-Associated Transcription FactorMITF protein, humanRNA, Messenger

Identifiers

PMID21460262
PMCPMC3176062
OpenAlexW1992915966

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.