Evidence map›Paper›PMID 24008408›Full record

ArticleInvestigative ophthalmology & visual science2013

CAP37 activation of PKC promotes human corneal epithelial cell chemotaxis.

Gina L Griffith, Robert A Russell, Anne Kasus-Jacobi, Elangovan Thavathiru, Melva L Gonzalez, Sreemathi Logan, H Anne Pereira

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Investigative ophthalmology & visual science, 2013. 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
1.9field-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

12 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Heparin-binding protein is important for vascular leak in sepsis.Intensive care medicine experimental · 2016
    Article
  8. Review
  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

7 authors at 1 institution in 1 country.

Gina L GriffithDepartment of Pathology, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma.
Robert A Russell
Anne Kasus-Jacobi
Elangovan Thavathiru
Melva L Gonzalez
Sreemathi Logan
H Anne Pereira
University of Oklahoma Health Sciences Center · US

Funding

Molecular Basis of Immunity - Kirschtein-NRSAT32AI007633 · NIAID · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI CUNNINGHAM, MADELEINE W. · 2001 to 2022
$4.0M
CAP37 and ocular inflammationR01EY015534 · NEI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI PEREIRA, HELOISE ANNE · 2007 to 2011
$1.8M
Wound healing mechanisms modulated by novel antimicrobial PeptidesR21EY026229 · NEI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI KASUS-JACOBI, ANNE · 2016 to 2017
$407k
NEI NIH HHS 5R01EY015534NEI NIH HHS R01 EY015534NEI NIH HHS R21 EY026229NIAID NIH HHS 5T32AI007633-08NIAID NIH HHS T32 AI007633
6 · The paper itself

Abstract

purposeThe objective of this study was to elucidate the signaling pathway through which cationic antimicrobial protein of 37 kDa (CAP37) mediates human corneal epithelial cell (HCEC) chemotaxis.

methodsImmortalized HCECs were treated with pertussis toxin (10 and 1000 ng/mL), protein kinase C (PKC) inhibitors (calphostin c, 50 nM and Ro-31-8220, 100 nM), phorbol esters (phorbol 12,13-dibutyrate, 200 nM and phorbol 12-myristate 13-acetate, 1 μM) known to deplete PKC isoforms, and siRNAs (400 nM) before a modified Boyden chamber assay was used to determine the effect of these inhibitors and siRNAs on CAP37-directed HCEC migration. PKCδ protein levels, PKCδ-Thr(505) phosphorylation, and PKCδ kinase activity was assessed in CAP37-treated HCECs using immunohistochemistry, Western blotting, and a kinase activity assay, respectively.

resultsChemotaxis studies revealed that treatment with pertussis toxin, PKC inhibitors, phorbol esters, and siRNAs significantly inhibited CAP37-mediated chemotaxis compared with untreated controls. CAP37 treatment increased PKCδ protein levels and led to PKCδ phosphorylation on residue Thr(505). Direct activation of PKCδ by CAP37 was demonstrated using a kinase activity assay.

conclusionsThese findings lead us to conclude that CAP37 is an important regulator of corneal epithelial cell migration and mediates its effects through PKCδ.

Indexed as

Enzyme ActivationAntimicrobial Cationic PeptidesBlood ProteinsBlotting, WesternCarrier ProteinsCells, CulturedChemotaxisEpithelium, CornealGlycoproteinsHumansImmunohistochemistryMicroscopy, ConfocalProtein Kinase CSignal TransductionAntimicrobial Cationic PeptidesAZU1 protein, humanBlood ProteinsCarrier ProteinsGlycoproteinsProtein Kinase Ccationic antimicrobial proteinsinflammationmigrationprotein kinase Csignaling

Identifiers

PMID24008408
PMCPMC3797592
OpenAlexW2086309021

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.