Evidence map›Paper›PMID 23792108›Full record

ArticleExperimental eye research2013

Role of phospholipase A₂ (PLA₂) inhibitors in attenuating apoptosis of the corneal epithelial cells and mitigation of Acanthamoeba keratitis.

Trivendra Tripathi, Mahshid Abdi, Hassan Alizadeh

Open access · greenAbstract read
In one paragraph

Article in Experimental eye research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

11 citing papers in PubMed, 25 citations in OpenAlex.

  1. Oxidative Stress and Redox Imbalance inInternational journal of molecular sciences · 2026
    Review
  2. Article
  3. Cytosolic phospholipase AScientific reports · 2020
    Article
  4. Pathobiology and Immunobiology ofThe Yale journal of biology and medicine · 2017
    Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. 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 1 country.

Trivendra TripathiDepartment of Cell Biology and Anatomy, University of North Texas Health Science Center, North Texas Eye Research Institute, 3500 Camp Bowie Blvd., Fort Worth, TX 76107, USA.
Mahshid Abdi
Hassan Alizadeh
University of North Texas · USUniversity of North Texas Health Science Center · US

Funding

BIOLOGY, IMMUNOLOGY &THERAPY OF ACANTHAMOEBA KERATITISR01EY009756 · NEI · UT SOUTHWESTERN MEDICAL CENTER · PI ALIZADEH, HASSAN · 1995 to 2013
$3.9M
NEI NIH HHS EY09756NEI NIH HHS R01 EY009756
6 · The paper itself

Abstract

The aim of this study is to determine if the mannose-induced protein (MIP-133) from Acanthamoeba castellanii trophozoites induces apoptosis of corneal epithelial cells through a cytosolic phospholipase A2α (cPLA2α)-mediated pathway. The efficacy of cPLA2α inhibitors to provide protection against Acanthamoeba keratitis was examined in vivo. Chinese hamster corneal epithelial (HCORN) cells were incubated with or without MIP-133. MIP-133 induces significant increase in cPLA2α and macrophage inflammatory protein-2 (MIP-2/CXCL2) levels from corneal cells. Moreover, cPLA2α inhibitors, MAFP (Methyl-arachidonyl fluorophosphonate) and AACOCF3 (Arachidonyl trifluoromethyl ketone), significantly reduce cPLA2α and CXCL2 from these cells (P < 0.05). Additionally, cPLA2α inhibitors significantly inhibit MIP-133-induced apoptosis in HCORN cells (P < 0.05). Subconjunctival injection of purified MIP-133 in Chinese hamster eyes induced cytopathic effects resulting in corneal ulceration. Animals infected with A. castellanii-laden contact lenses and treated with AACOCF3 and CAY10650, showed significantly less severe keratitis as compared with control animals. Collectively, the results indicate that cPLA2α is involved in MIP-133 induced apoptosis of corneal epithelial cells, polymorphonuclear neutrophil infiltration, and production of CXCL2. Moreover, cPLA2α inhibitors can be used as a therapeutic target in Acanthamoeba keratitis.

Indexed as

Acanthamoeba castellaniiAcanthamoeba KeratitisAnimalsApoptosisArachidonic AcidsBlotting, WesternCells, CulturedChemokine CXCL2Chromatography, High Pressure LiquidConjunctivaCricetinaeCricetulusDisease Models, AnimalEnzyme InhibitorsEnzyme-Linked Immunosorbent AssayEpithelium, CornealArachidonic AcidsarachidonyltrifluoromethaneChemokine CXCL2Enzyme InhibitorsMannosemannose-induced cytopathic protein 133, Acanthamoebamethyl arachidonylfluorophosphonateOrganophosphonatesPhospholipases A2, CytosolicProtozoan ProteinsRNA, MessengerAcanthamoebaChinese hamstercorneal epithelial cellscytosolic phospholipase A(2α)keratitismacrophage inflammatory protein-2mannose-induced protein

Identifiers

PMID23792108
PMCPMC3742089
OpenAlexW2025254130

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.