Evidence map›Paper›PMID 8623913›Full record

ArticleThe American journal of pathology1996

Transient functional expression of alphaVbeta 3 on vascular cells during wound repair.

R A Clark, M G Tonnesen, J Gailit, D A Cheresh

Abstract read
In one paragraph

Article in The American journal of pathology, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

53 citing papers in PubMed, 198 citations in OpenAlex.

  1. Review
  2. Endothelial αvβ3 integrin induction during hypoxia protects blood-brain barrier integrity.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. BioMed research international · 2020
    Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. In situ observation and enhancement of leaflet tissue formation in bioprosthetic "biovalve".Journal of artificial organs : the official journal of the Japanese Society for Artificial Organs · 2015
    Article
  16. Review
  17. Article
  18. Article
  19. Antagonizing the αv β3 integrin inhibits angiogenesis and impairs woven but not lamellar bone formation induced by mechanical loading.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2014
    Article
  20. 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

4 authors at 1 institution in 1 country.

R A ClarkDepartment of Dermatology, State University of New York at Stony Brook, 11794-8165, USA.
M G Tonnesen
J Gailit
D A Cheresh
Stony Brook University · US

Funding

REGULATION OF TUMOR CELL ATTACHMENT BY SURFACE ANTIGENSR01CA045726 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CHERESH, DAVID A · 1988 to 2017
$7.4M
VEGF and PDGF in angiogenesis and tumor progressionR37CA050286 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CHERESH, DAVID A · 1999 to 2013
$6.3M
FIBRONECTIN AND CELL RECRUITMENTR37AG010143 · NIA · STATE UNIVERSITY NEW YORK STONY BROOK · PI CLARK, RICHARD AUGUST · 1996 to 2005
$2.4M
STRUCTURAL AND FUNCTIONAL STUDIES--INTEGERIN-DEPENDENTR01CA050286 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CHERESH, DAVID A · 1989 to 2018
$1.9M
FIBRONECTIN AND CELL RECRUITMENTR01AG010143 · NIA · STATE UNIVERSITY NEW YORK STONY BROOK · PI CLARK, RICHARD AUGUST · 1991 to 1996
–
NCI NIH HHS CA45726NCI NIH HHS CA50286NIA NIH HHS AG10143
6 · The paper itself

Abstract

During early granulation tissue formation of wound repair, new capillaries invade the fibrin clot, a process that undoubtedly requires an interaction of vascular cells with the wound provisional matrix composed mainly of fibrin, fibronectin, and vitronectin. Integrin alphaVbeta3 is the vascular cell receptor for these wound-associated adhesive proteins. Therefore, we investigated the expression of this receptor on new capillaries of healing full-thickness cutaneous porcine wounds. During granulation tissue formation, alphaVbeta3 was expressed specifically on capillary sprouts invading the central fibrin clot whereas the closely related integrin alphaVbeta5 failed to localize to these cells. Cyclic peptides or antibody antagonists of alphaVbeta3 specifically inhibited granulation tissue formation in a transient manner during the period of invasive angiogenesis. Immunolocalization studies revealed that alphaVbeta3 became aggregated and lost from sprouting vessels after treatment with a peptide antagonist. In contrast, beta 1 integrins were not modulated by this treatment. Once granulation tissue filled the wound and invasive angiogenesis terminated, the alphaVbeta3 showed little or no expression in the granulation tissue microvasculature. These data demonstrate that integrin alphaVbeta3 plays a fundamental, but transient, role during invasive angiogenesis and granulation tissue formation in a healing wound.

Indexed as

Analysis of VarianceAnimalsCapillariesEndothelium, VascularFibrinFibrinogenGranulation TissueNeovascularization, PhysiologicReceptors, VitronectinSwineSwine, MiniatureVitronectinWound HealingFibrinFibrinogenReceptors, VitronectinVitronectin

Identifiers

PMID8623913
PMCPMC1861547
OpenAlexW274201170

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.