Evidence map›Paper›PMID 17591888›Full record

ArticleInvestigative ophthalmology & visual science2007

Presence of an established calcification marker in trabecular meshwork tissue of glaucoma donors.

Wei Xue, Núria Comes, Teresa Borrás

Open access · greenAbstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

40 citing papers in PubMed, 64 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. 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
  13. Article
  14. Review
  15. Human Trabecular Meshwork Progenitors.International journal of medical sciences · 2019
    Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. Review
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 1 institution in 1 country.

Wei XueDepartment of Ophthalmology, University of North Carolina School of Medicine, Chapel Hill, North Carolina 27599-7041, USA.
Núria Comes
Teresa Borrás
University of North Carolina at Chapel Hill · US

Funding

REGULATION OF OUTFLOW FACILITY BY GENE TRANSFERR01EY011906 · NEI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BORRAS, TERESA · 1997 to 2016
$5.6M
PRESSURE REGULATION OF HUMAN TRABECULAR MESHWORK GENESR01EY013126 · NEI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BORRAS, TERESA · 2000 to 2012
$4.1M
NEI NIH HHS EY11906NEI NIH HHS EY13126NEI NIH HHS R01 EY011906NEI NIH HHS R01 EY013126
6 · The paper itself

Abstract

purposeTo determine the presence of calcification markers in the trabecular meshwork tissue from glaucoma donors and in trabecular meshwork cells insulted by dexamethasone (DEX) and transforming growth factor beta2 (TGFbeta2), factors associated with glaucoma. To investigate as well the effect of silencing the inhibitor of calcification matrix Gla (MGP) in the trabecular meshwork cells.

methodsTrabecular meshwork tissue was obtained from perfused postmortem anterior segments of glaucomatous and normal eyes. Primary trabecular meshwork cells were obtained from residual corneal rims after surgical corneal transplantation. Calcification marker alkaline phosphatase (ALP) enzyme activity was assayed by fluorescence produced after substrate cleavage. DNA quantification was evaluated by fluorescence produced after binding to the Hoechst dye. Transfection of siRNA to primary cells was accomplished by nucleofector electroporation with trabecular meshwork-optimized conditions. cDNA quantification was performed with the use of TaqMan real-time PCR.

resultsHuman trabecular meshworks from glaucoma donors exhibited significantly higher levels of ALP activity than their matched counterparts with normal eyes. The normalized ALP of the control specimens was 7.3 +/- 1.6 ng ALP/microg DNA (n = 4), whereas that of the glaucomatous tissue was 37.0 +/- 10.7 ng ALP/microg genomic DNA (n = 5; P </= 0.04). DEX and TGFbeta2 significantly induced the upregulation of ALP activity in two trabecular meshwork primary cell lines. Expression of the gene encoding MGP was reduced in the glaucomatous tissue by -4.4 +/- 1.7-fold (n = 9; P </= 0.006). Silencing MGP by siRNA resulted in ALP activity that was increased by 197% +/- 8.4% (P </= 0.0003).

conclusionsThe increased activity of the calcification marker, ALP, in glaucomatous trabecular meshworks might be indicative of an undergoing mineralization process during development of the disease. Inhibition of the calcification mechanism represented by the presence of active MGP appears to be compromised in glaucomatous tissue.

Indexed as

AdultAgedAged, 80 and overAlkaline PhosphataseBiomarkersCalcinosisCalcium-Binding ProteinsCells, CulturedDexamethasoneElectroporationExtracellular Matrix ProteinsFemaleGene SilencingGlaucomaHumansMaleAlkaline PhosphataseBiomarkersCalcium-Binding ProteinsDexamethasoneExtracellular Matrix ProteinsMatrix Gla ProteinRNA, Small InterferingTransforming Growth Factor beta2

Identifiers

PMID17591888
PMCPMC1994153
OpenAlexW2087070388

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.