Evidence map›Paper›PMID 27939447›Full record

ArticleExperimental eye research2017

Differential response and withdrawal profile of glucocorticoid-treated human trabecular meshwork cells.

Guorong Li, Gang Cui, W Michael Dismuke, Iris Navarro, Kristin Perkumas, David F Woodward, W Daniel Stamer

Open access · greenAbstract read
In one paragraph

Article in Experimental eye research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.9field-weighted citation impact, top 23% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Identification of Gene Changes Induced by Dexamethasone in the Anterior Segment of the Human Eye Using Bioinformatics Analysis.Medical science monitor : international medical journal of experimental and clinical research · 2019
    Article
  8. Review
  9. 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

7 authors at 3 institutions in 2 countries.

Guorong LiDepartment of Ophthalmology, Duke University, Durham, NC, United States.
Gang CuiUniversity of North Carolina at Chapel Hill, Collaborative Studies Coordinating Center, United States.
W Michael DismukeDepartment of Ophthalmology, Duke University, Durham, NC, United States.
Iris NavarroDepartment of Ophthalmology, Duke University, Durham, NC, United States.
Kristin PerkumasDepartment of Ophthalmology, Duke University, Durham, NC, United States.
David F WoodwardDepartment of Bioengineering, Imperial College London, UK.
W Daniel StamerDepartment of Ophthalmology, Duke University, Durham, NC, United States. Electronic address: dan.stamer@duke.edu.
Duke University · USImperial College London · GBUniversity of North Carolina at Chapel Hill · US

Funding

VISION RESEARCHP30EY005722 · NEI · DUKE UNIVERSITY · PI Vadim Y Arshavsky · 1985 to 2026
$19.3M
The Mechanical Basis of Primary Open Angle GlaucomaR01EY019696 · NEI · NORTHWESTERN UNIVERSITY · PI FREDBERG, JEFFREY J, JOHNSON, MARK · 2009 to 2019
$7.6M
NEI NIH HHS P30 EY005722NEI NIH HHS R01 EY019696
6 · The paper itself

Abstract

The goal of the study was to examine secreted protein response and withdrawal profiles from cultured human trabecular meshwork (HTM) cells following short- and long-term glucocorticoid treatment. Primary cultures of five human HTM cell strains isolated from 5 different individual donor eyes were tested. Confluent HTM cells were differentiated in culture media containing 1% FBS for at least one week, and then treated with Dexamethasone (Dex, 100 nM) 3 times/week for 1 or 4 weeks. Cell culture supernatants were collected 3 times per week for 8 weeks. Secretion profiles of myocilin (MYOC), matrix metalloproteinase-2 (MMP2) and fibronectin (FN) were determined by Western blot analysis and MMP2 activity by zymography. Dex treatment reduced MMP2 expression and activity, returning to normal levels shortly after Dex withdrawal in 5 HTM cell strains. All five cell strains significantly upregulated MYOC in response to Dex treatment by an average of 17-fold, but recovery to basal levels after Dex withdrawal took vastly different periods of time depending on cell strain and treatment duration. Dex treatment significantly increased FN secretion in all strains but one, which decreased FN secretion in the presence of Dex. Interestingly, secretion of FN and MYOC negatively correlated during a 4 week recovery period following 4 weeks of Dex treatment. Taken together, the time course and magnitude of response and recovery for three different secreted, extracellular matrix-associated proteins varied greatly between HTM cell strains, which may underlie susceptibility to glucocorticoid-induced ocular hypertension.

Indexed as

AdultAgedAged, 80 and overBlotting, WesternCells, CulturedCytoskeletal ProteinsDexamethasoneExtracellular Matrix ProteinsEye ProteinsGlucocorticoidsGlycoproteinsHumansInfantMyocilinOcular HypertensionTissue DonorsCytoskeletal ProteinsDexamethasoneExtracellular Matrix ProteinsEye ProteinsGlucocorticoidsGlycoproteinsMyocilinConventional outflowDexamethasoneExtracellular matrixGlaucomaOcular hypertension

Identifiers

PMID27939447
PMCPMC5359060
OpenAlexW2559804003

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.