Evidence map›Paper›PMID 24135023›Full record

ArticleArteriosclerosis, thrombosis, and vascular biology2013

Pericyte regulation of vascular remodeling through the CXC receptor 3.

Richard J Bodnar, Margaret E Rodgers, William C W Chen, Alan Wells

Open access · bronzeAbstract read
In one paragraph

Article in Arteriosclerosis, thrombosis, and vascular biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

38 citing papers in PubMed, 69 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Physiological and Pathological Remodeling of Cerebral Microvessels.International journal of molecular sciences · 2022
    Review
  10. CD146International journal of molecular sciences · 2022
    Article
  11. Is Long COVID a State of Systemic Pericyte Disarray?Journal of clinical medicine · 2022
    Article
  12. Review
  13. Review
  14. Review
  15. Article
  16. Pericytes in Vascular Development.Current tissue microenvironment reports · 2020
    Article
  17. Review
  18. Characterization of Burn Eschar Pericytes.Journal of clinical medicine · 2020
    Article
  19. Article
  20. Oxygen and nutrient delivery in tissue engineering: Approaches to graft vascularization.Journal of tissue engineering and regenerative medicine · 2019
    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

4 authors at 1 institution in 1 country.

Richard J BodnarFrom the Department of Pathology (R.J.B., M.E.B., A.W.) and Department of Bioengineering (W.C.W.C.), University of Pittsburgh, PA; and Pittsburgh Veterans Affairs Medical Center, Pittsburgh, PA (R.J.B., M.E.B., A.W.).
Margaret E Rodgers
William C W Chen
Alan Wells
University of Pittsburgh Medical Center · US

Funding

Spatial Segregation of Cell Functioning During MotilityR01GM069668 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WELLS, ALAN · 2004 to 2019
$4.7M
Dermal-Epidermal Communication during Wound HealingR01GM063569 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WELLS, ALAN · 2003 to 2018
$3.7M
NIGMS NIH HHS R01 GM063569NIGMS NIH HHS R01 GM069668
6 · The paper itself

Abstract

objectiveTo understand the role, if any, played by pericytes in the regulation of newly formed vessels during angiogenesis. In this study, we investigate whether pericytes regulate the number of nascent endothelial tubes. APPROACH AND

resultsUsing an in vitro angiogenesis assay (Matrigel assay), we demonstrate that pericytes can inhibit vessel formation and induce vessel dissociation via CXCR3-induced involution of the endothelial cells. In a coculture Matrigel assay for cord formation, pericytes prevented endothelial cord formation of human dermal microvascular endothelial cells but not umbilical vein endothelial cells. Blockade of endothelial CXCR3 function or expression inhibited the repressing effect of the pericytes. We further show that pericytes are also able to induce regression of newly formed microvascular cords through CXCR3 activation of calpain. When CXCR3 function was inhibited by a neutralizing antibody or downregulated by siRNA, cord regression mediated by pericytes was abolished.

conclusionsWe show for the first time that pericytes regulate angiogenic vessel formation, and that this is mediated through CXCR3 expressed on endothelial cells. This suggests a role for pericytes in the pruning of immature vessels overproduced during wound repair.

Indexed as

Cell CommunicationNeovascularization, PhysiologicCalpainCells, CulturedCoculture TechniquesEndothelial CellsEnzyme ActivationHumansHuman Umbilical Vein Endothelial CellsInterferon-gammaLigandsPericytesReceptors, CXCR3RNA InterferenceSignal TransductionTime FactorsCalpainCXCR3 protein, humanInterferon-gammaLigandsReceptors, CXCR3angiogenesisCXC chemokine receptor 3endothelial cellspericyteswound healing

Identifiers

PMID24135023
PMCPMC4591000
OpenAlexW2005177372

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.