Evidence map›Paper›PMID 19474402›Full record

ArticleInvestigative ophthalmology & visual science2009

Retinal endothelial cell apoptosis stimulates recruitment of endothelial progenitor cells.

Ashay D Bhatwadekar, Josephine V Glenn, Tim M Curtis, Maria B Grant, Alan W Stitt, Tom A Gardiner

Abstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 2009. 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
0.7field-weighted citation impact, top 31% 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, 25 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Association of Extracellular Membrane Vesicles with Cutaneous Wound Healing.International journal of molecular sciences · 2017
    Review
  7. Review
  8. Review
  9. Molecular imaging of retinal disease.Journal of ocular pharmacology and therapeutics : the official journal of the Association for Ocular Pharmacology and Therapeutics · 2013
    Review
  10. Article
  11. Cell-based therapies for diabetic retinopathy.Current diabetes reports · 2011
    Review
  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 4 institutions in 2 countries.

Ashay D BhatwadekarCentre for Vision Science, Queen's University Belfast, Royal Victoria Hospital, Belfast, Northern Ireland, United Kingdom.
Josephine V Glenn
Tim M Curtis
Maria B Grant
Alan W Stitt
Tom A Gardiner
University of Florida · USUniversity of Ulster · GBQueen's University Belfast · GBRoyal Victoria Hospital · GB

Funding

NITRIC OXIDE IN THE PATHOGENESIS OF DIABETIC RETINOPATHYR01EY012601 · NEI · UNIVERSITY OF FLORIDA · PI Julia V Busik, Maria Bartolomeo Grant · 1998 to 2026
$9.6M
Targeting the IGF-1 System in Retinal AngiogenesisR01EY007739 · NEI · UNIVERSITY OF FLORIDA · PI ABCOUWER, STEVEN F, GRANT, MARIA BARTOLOMEO · 1995 to 2015
$5.4M
NO Dysregulation of the Peripheral Clock in Diabetic ComplicationsR01DK090730 · NIDDK · UNIVERSITY OF FLORIDA · PI GRANT, MARIA BARTOLOMEO · 2010 to 2013
$1.3M
CXCR4/SDF-1 Axis in Proliferation Diabetic RetinopathyR21EY014818 · NEI · UNIVERSITY OF FLORIDA · PI GRANT, MARIA BARTOLOMEO · 2002 to 2003
$725k
Medical Research CouncilNEI NIH HHS R01 EY007739NEI NIH HHS R01 EY012601NEI NIH HHS R21 EY014818NIDDK NIH HHS R01 DK090730
6 · The paper itself

Abstract

purposeBone marrow-derived endothelial progenitor cells (EPCs) contribute to vascular repair although it is uncertain how local endothelial cell apoptosis influences their reparative function. This study was conducted to determine how the presence of apoptotic bodies at sites of endothelial damage may influence participation of EPCs in retinal microvascular repair.

methodsMicrolesions of apoptotic cell death were created in monolayers of retinal microvascular endothelial cells (RMECs) by using the photodynamic drug verteporfin. The adhesion of early-EPCs to these lesions was studied before detachment of the apoptotic cells or after their removal from the wound site. Apoptotic bodies were fed to normal RMECs and mRNA levels for adhesion molecules were analyzed.

resultsEndothelial lesions where apoptotic bodies were left attached at the wound site showed a fivefold enhancement in EPC recruitment (P < 0.05) compared with lesions where the apoptotic cells had been removed. In intact RMEC monolayers exposed to apoptotic bodies, expression of ICAM, VCAM, and E-selectin was upregulated by 5- to 15-fold (P < 0.05-0.001). EPCs showed a characteristic chemotactic response (P < 0.05) to conditioned medium obtained from apoptotic bodies, whereas analysis of the medium showed significantly increased levels of VEGF, IL-8, IL-6, and TNF-alpha when compared to control medium; SDF-1 remained unchanged.

conclusionsThe data indicate that apoptotic bodies derived from retinal capillary endothelium mediate release of proangiogenic cytokines and chemokines and induce adhesion molecule expression in a manner that facilitates EPC recruitment.

Indexed as

ApoptosisAnimalsCapillariesCattleCell AdhesionCell MovementCells, CulturedChemotaxisCytokinesEndothelium, VascularEnzyme-Linked Immunosorbent AssayE-SelectinFlow CytometryFluorescent Antibody Technique, IndirectIntercellular Adhesion Molecule-1Photosensitizing AgentsCytokinesE-SelectinIntercellular Adhesion Molecule-1Photosensitizing AgentsPorphyrinsRNA, MessengerVascular Cell Adhesion Molecule-1Vascular Endothelial Growth Factor AVerteporfin

Identifiers

PMID19474402
PMCPMC3766363
OpenAlexW2053786238

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.