Evidence map›Paper›PMID 25082886›Full record

ArticleInvestigative ophthalmology & visual science2014

The Zeb proteins δEF1 and Sip1 may have distinct functions in lens cells following cataract surgery.

Abby L Manthey, Anne M Terrell, Yan Wang, Jennifer R Taube, Alisha R Yallowitz, Melinda K Duncan

Open access · bronzeAbstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.4field-weighted citation impact, top 35% 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

12 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Modeling Cataract Surgery in Mice.Journal of visualized experiments : JoVE · 2023
    Article
  6. Article
  7. Article
  8. The aging mouse lens transcriptome.Experimental eye research · 2021
    Article
  9. Article
  10. Article
  11. Article
  12. 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

6 authors at 1 institution in 1 country.

Abby L MantheyDepartment of Biological Sciences, University of Delaware, Newark, Delaware, United States.
Anne M TerrellDepartment of Biological Sciences, University of Delaware, Newark, Delaware, United States.
Yan WangDepartment of Biological Sciences, University of Delaware, Newark, Delaware, United States.
Jennifer R TaubeDepartment of Biological Sciences, University of Delaware, Newark, Delaware, United States.
Alisha R YallowitzDepartment of Biological Sciences, University of Delaware, Newark, Delaware, United States.
Melinda K DuncanDepartment of Biological Sciences, University of Delaware, Newark, Delaware, United States.
University of Delaware · US

Funding

Predictive Modeling & Optimal Control Framework for Model-Based Epidemic Response in DelawareP20GM103446 · NIGMS · UNIVERSITY OF DELAWARE · PI Anjana Narayan Bhat · 2012 to 2026
$67.2M
The Regulation of Lens Fiber Cell DifferentiationR01EY012221 · NEI · UNIVERSITY OF DELAWARE · PI DUNCAN, MELINDA K · 1998 to 2012
$3.7M
Howard Hughes Medical InstituteNEI NIH HHS EY12221NEI NIH HHS R01 EY012221NIGMS NIH HHS GM103446NIGMS NIH HHS P20 GM103446
6 · The paper itself

Abstract

purposePosterior capsular opacification (PCO), the most prevalent side effect of cataract surgery, occurs when residual lens epithelial cells (LECs) undergo fiber cell differentiation or epithelial-to-mesenchymal transition (EMT). Here, we used a murine cataract surgery model to investigate the role of the Zeb proteins, Smad interacting protein 1 (Sip1) and δ-crystallin enhancer-binding factor 1 (δEF1), during PCO.

methodsExtracapsular extraction of lens fiber cells was performed on wild-type and Sip1 knockout mice. Protein expression patterns were assessed at multiple time points after surgery using confocal immunofluorescence. βB1-Crystallin mRNA levels were measured using quantitative RT-PCR. We used Transfac searches to identify δEF1 binding sites in the βB1-crystallin promoter and transfection analysis to test the ability of δEF1 to regulate βB1-crystallin expression.

resultsδEF1, which, in other systems, can activate fibrotic genes (e.g., α-smooth muscle actin) and repress epithelial genes, upregulates by 48 hours after fiber cell removal. In culture, δEF1 repressed βB1-crystallin promoter activity, suggesting that it may also turn off lens gene expression following surgery, contributing to "fibrotic PCO" development. Sip1 also upregulates in LECs by 48 hours, but analysis of Sip1 knockout lenses demonstrated that Sip1 does not play a major role in EMT or fiber cell differentiation after surgery. However, Sip1 knockout LECs do express the ectodermal marker keratin 8, suggesting that Sip1 may limit the reprogramming of residual LECs to an embryonic state.

conclusionsZeb transcription factors likely play important, but distinct roles in PCO development after cataract surgery.

Indexed as

AnimalsCataractCataract ExtractionDisease Models, AnimalHomeodomain ProteinsLens, CrystallineMice, KnockoutNerve Tissue ProteinsPostoperative ComplicationsRNA, MessengerTranscription FactorsZinc Finger E-box-Binding Homeobox 1Homeodomain ProteinsNerve Tissue ProteinsRNA, MessengerSip1 protein, mouseTranscription FactorsZEB1 protein, mouseZinc Finger E-box-Binding Homeobox 1cataract surgeryepithelial-to-mesenchymal transitionlens regenerationmouse disease modelposterior capsular opacificationZeb

Identifiers

PMID25082886
PMCPMC4148927
OpenAlexW2323231913

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.