Evidence map›Paper›PMID 21139686›Full record

ArticleMolecular vision2010

Gene expression analysis in SV-40 immortalized human corneal epithelial cells cultured with an air-liquid interface.

Dario Greco, Kati-Sisko Vellonen, Helen C Turner, Marika Häkli, Timo Tervo, Petri Auvinen, J Mario Wolosin, Arto Urtti

Open access · greenAbstract read
In one paragraph

Article in Molecular vision, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

19 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
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  5. The Biocompatibility Analysis of Artificial Mucin-Like Glycopolymers.International journal of molecular sciences · 2023
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  9. Review
  10. HCE-T cell line lacks cornea-specific differentiation markers compared to primary limbal epithelial cells and differentiated corneal epithelium.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2020
    Article
  11. Article
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  14. Human corneal cell culture models for drug toxicity studies.Drug delivery and translational research · 2016
    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

8 authors at 2 institutions in 2 countries.

Dario GrecoInstitute of Biotechnology, Centre for Drug Research, Department of Ophthalmology, University of Helsinki, Helsinki, Finland.
Kati-Sisko Vellonen
Helen C Turner
Marika Häkli
Timo Tervo
Petri Auvinen
J Mario Wolosin
Arto Urtti
Mount Sinai Hospital · USCzech Academy of Sciences, Institute of Biotechnology · CZ

Funding

OCULAR SURFACE EPITHELIAL PRECURSORSR01EY014878 · NEI · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI WOLOSIN, JOSE MARIO · 2005 to 2015
$4.1M
NEI NIH HHS EY 01478NEI NIH HHS R01 EY014878
6 · The paper itself

Abstract

purposeTo compare the global gene expression profile of stratified epithelia generated in vitro using simian virus 40 (SV40) immortalized human corneal epithelial cells with the previously reported gene expression of normal human corneal epithelia.

methodsImmortalized cells expanded in submerged culture were grown in an air-liquid interface of liquid permeable collagen-coated filters to foster stratification and differentiation. Stratified epithelia displaying resistances exceeding 300 Ω·cm2 were dissolved in an RNA purification lysis buffer. Purified RNA was used to globally determine gene expression levels using high-density single-channel oligonucleotide microarrays. Raw hybridization readings were converted into relative gene expression levels using Robust Multi-array Average (RMA) algorithm. Expression levels for selected genes were validated by real-time RT-qPCR. The biologic significance of the gene expression profiles was interpreted with the help of several microarray software analysis tools and ad hoc thematical analysis.

resultsThe stratified cell culture to native epithelial comparison identified over- and under-expression in 22% and 14% of the probed genes, respectively. The larger expression decreases occurred in genes intimately associated with both the stratified epithelial lineage at large such as keratin 14 and the corneal phenotype, such as keratin 12, connexin 43, aldehyde dehydrogenases (ALDHs), and paired box gene 6 (PAX6) and its whole downstream transcriptome. Overexpression related to genes associated with cell cycling stimulation.

conclusionsThe results indicate that the stratified corneal epithelial cell model generated using SV40 immortalized cells may be useful only in certain research applications. Extrapolations of studies with these cells to actual tissue cells should be done with a great deal of caution.

Indexed as

Gene Expression ProfilingCell Culture TechniquesCell LineageCell Line, TransformedEpithelial CellsEpithelium, CornealHumansOligonucleotide Array Sequence AnalysisOrgan SpecificityReproducibility of ResultsReverse Transcriptase Polymerase Chain ReactionRNARNA, MessengerSimian virus 40Up-RegulationRNARNA, Messenger

Identifiers

PMID21139686
PMCPMC2994346
OpenAlexW2155841673

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.