Evidence map›Paper›PMID 18757513›Full record

ArticleInvestigative ophthalmology & visual science2009

Role of cell and matrix-bound VEGF isoforms in lens development.

Magali Saint-Geniez, Tomoki Kurihara, Patricia A D'Amore

Open access · greenAbstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 12% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Pooled it
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  4. Review
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  10. Expression and role of VEGF--a in the ciliary body.Investigative ophthalmology & visual science · 2012
    Article
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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

3 authors at 2 institutions in 2 countries.

Magali Saint-GeniezSchepens Eye Research Institute, Boston, MA 02114, USA.
Tomoki Kurihara
Patricia A D'Amore
Singapore Eye Research Institute · SGHarvard University · US

Funding

P30 Core Grant for Vision ResearchP30EY014104 · NEI · MASSACHUSETTS EYE AND EAR INFIRMARY · PI Eric A Pierce · 2002 to 2026
$15.1M
THE ROLE OF MICROVASCULAR CELLS IN NEOVASCULARIZATIONR01EY005318 · NEI · SCHEPENS EYE RESEARCH INSTITUTE · PI D'AMORE, PATRICIA ANN · 1985 to 2015
$6.4M
Role of RPE-derived VEGF in Choroid Development and StabilityR01EY015435 · NEI · SCHEPENS EYE RESEARCH INSTITUTE · PI D'AMORE, PATRICIA ANN · 2004 to 2013
$4.3M
NEI NIH HHS EY005318NEI NIH HHS EY015435NEI NIH HHS P30 EY014104NEI NIH HHS P30EY14104NEI NIH HHS R01 EY005318NEI NIH HHS R01 EY015435
6 · The paper itself

Abstract

purposeTo determine the role of vascular endothelial growth factor (VEGF) in embryonic eye development and lens differentiation.

methodsExpression of components of the VEGF signaling pathway during lens development and in adults was characterized by beta-galactosidase staining of VEGF-LacZ mice, immunohistochemistry, and real-time (q) PCR. Embryonic eyes from wild-type mice and VEGF120/120 mice were analyzed by light microscopy and immunohistochemistry. VEGF function during lens development was analyzed using eye explants treated with VEGF-neutralizing antibody. Direct function of VEGF was demonstrated on the human lens epithelial cell line, HLE-B3.

resultsEmbryonic lens epithelium and posterior lens fibers expressed VEGF and VEGFR2. qPCR revealed VEGF164 as the major isoform in embryonic lens. Transgenic mice expressing only VEGF120 (VEGF120/120 mice) showed major defects in eye development, including microphthalmia, failed lens differentiation, and hyperplastic hyaloid vessels. The lens displayed abnormal cell patterning and differentiation associated with altered c-Maf, Prox1, and p57 expression pattern in the anterior epithelium. The number of proliferating epithelial cells was drastically reduced in VEGF120/120 lenses. Altered MIP26 cellular localization and reduced E-cadherin expression in the lens epithelium were observed. VEGF-neutralization led to reduced fiber elongation of eye explants. Exogenous VEGF increased survival and proliferation of HLE-B3 cell in a dose-dependent manner.

conclusionsAbnormalities in ocular development in VEGF120/120 mice suggest a role for VEGF not only in the formation of ocular vascular beds but also in the differentiation of the lens itself.

Indexed as

AnimalsAquaporinsCadherinsCell DifferentiationCell LineCyclin-Dependent Kinase Inhibitor p57Epithelial CellsEye ProteinsFemaleFluorescent Antibody Technique, IndirectGene Expression Regulation, DevelopmentalHomeodomain ProteinsHumansImmunoenzyme TechniquesLens, CrystallineMiceaquaporin 0AquaporinsCadherinsCdkn1c protein, mouseCyclin-Dependent Kinase Inhibitor p57Eye ProteinsHomeodomain ProteinsMaf protein, mouseProspero-Related Homeobox 1 ProteinProtein IsoformsProto-Oncogene Proteins c-mafTumor Suppressor ProteinsVascular Endothelial Growth Factor Avascular endothelial growth factor A, mouseVascular Endothelial Growth Factor Receptor-2

Identifiers

PMID18757513
PMCPMC8259621
OpenAlexW2041749948

What OpenQuestion holds

Textmetadata
LicenceTDM
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.