Evidence map›Paper›PMID 24969773›Full record

ArticleArteriosclerosis, thrombosis, and vascular biology2014

Monocytes are recruited from venules during arteriogenesis in the murine spinotrapezius ligation model.

Anthony C Bruce, Molly R Kelly-Goss, Joshua L Heuslein, Joshua K Meisner, Richard J Price, Shayn M Peirce

Abstract read
In one paragraph

Article in Arteriosclerosis, thrombosis, and vascular biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
–field-weighted citation impact
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

21 citing papers in PubMed.

  1. Review
  2. Target and Cell Therapy for Atherosclerosis and CVD.International journal of molecular sciences · 2023
    Review
  3. Role of Vascular Smooth Muscle Cell Phenotype Switching in Arteriogenesis.International journal of molecular sciences · 2021
    Review
  4. Article
  5. Article
  6. NFAT5 promotes arteriogenesis via MCP-1-dependent monocyte recruitment.Journal of cellular and molecular medicine · 2020
    Article
  7. 7-Biomolecules · 2019
    Article
  8. Article
  9. Article
  10. Tissue Engineering the Vascular Tree.Tissue engineering. Part B, Reviews · 2017
    Review
  11. Article
  12. Arteriogenesis in murine adipose tissue is contingent on CD68Microcirculation (New York, N.Y. : 1994) · 2017
    Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. 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

6 authors.

Anthony C BruceFrom the Department of Biomedical Engineering, University of Virginia, Charlottesville.
Molly R Kelly-GossFrom the Department of Biomedical Engineering, University of Virginia, Charlottesville.
Joshua L HeusleinFrom the Department of Biomedical Engineering, University of Virginia, Charlottesville.
Joshua K MeisnerFrom the Department of Biomedical Engineering, University of Virginia, Charlottesville.
Richard J PriceFrom the Department of Biomedical Engineering, University of Virginia, Charlottesville.
Shayn M PeirceFrom the Department of Biomedical Engineering, University of Virginia, Charlottesville. smp6p@virginia.edu.

Funding

BASIC CARDIOVASCULAR RESEARCH TRAINING GRANTT32HL007284 · NHLBI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI Brant E Isakson, Gary K Owens · 1985 to 2026
$19.6M
MEDICAL SCIENTIST TRAINING PROGRAMT32GM007267 · NIGMS · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI GARCIA-BLANCO, MARIANO A. · 1985 to 2024
$13.4M
Arteriole/Venule Polarity in Adult MicrovasculatureR01HL082838 · NHLBI · UNIVERSITY OF VIRGINIA · PI PEIRCE-COTTLER, SHAYN · 2007 to 2011
$1.9M
Phospholipid Growth Factors for Therapeutic Arteriogenesis and Tissue EngineeringR01AR056445 · NIAMS · UNIVERSITY OF VIRGINIA · PI BOTCHWEY, EDWARD A. · 2009 to 2014
$1.8M
Application of Laser Speckle Flowmetry to Vascular RemodelingR03EB017927 · NIBIB · UNIVERSITY OF VIRGINIA · PI PRICE, RICHARD J. · 2014 to 2015
$153k
NHLBI NIH HHS HL082838NHLBI NIH HHS R01 HL082838NHLBI NIH HHS T32 HL007284NIAMS NIH HHS R01 AR056445NIBIB NIH HHS R03 EB017927
6 · The paper itself

Abstract

objectiveChronic arterial occlusion results in arteriogenesis of collateral blood vessels. This process has been shown to be dependent on the recruitment of growth-promoting macrophages to remodeling collaterals. However, the potential role of venules in monocyte recruitment during microvascular arteriogenesis is not well demonstrated. First, we aim to document that arteriogenesis occurs in the mouse spinotrapezius ligation model. Then, we investigate the temporal and spatial distribution, as well as proliferation, of monocytes/macrophages recruited to collateral arterioles in response to elevated fluid shear stress. APPROACH AND

resultsLaser speckle flowmetry confirmed a postligation increase in blood velocity within collateral arterioles but not within venules. After 72 hours post ligation, collateral arteriole diameters were increased, proliferating cells were identified in vessel walls of shear-activated collaterals, and perivascular CD206(+) macrophages demonstrated proliferation. A 5-ethynyl-2'-deoxyuridine assay identified proliferation. CD68(+)CD206(+) cells around collaterals were increased 96%, whereas CX3CR1((+/GFP)) cells were increased 126% in ligated versus sham groups after 72 hours. CX3CR1((+/GFP)) cells were predominately venule associated at 6 hours after ligation; and CX3CR1((+/GFP hi)) cells shifted from venule to arteriole associated between 6 and 72 hours after surgery exclusively in ligated muscle. We report accumulation and extravasation of adhered CX3CR1((+/GFP)) cells in and from venules, but not from arterioles, after ligation.

conclusionsOur results demonstrate that arteriogenesis occurs in the murine spinotrapezius ligation model and implicate postcapillary venules as the site of tissue entry for circulating monocytes. Local proliferation of macrophages is also documented. These data open up questions about the role of arteriole-venule communication during monocyte recruitment.

Indexed as

AnimalsAntigens, CDAntigens, Differentiation, MyelomonocyticArteriolesCD68 MoleculeCell DivisionCX3C Chemokine Receptor 1Endothelium, VascularFemaleGenes, ReporterHemorheologyIschemiaLaser-Doppler FlowmetryLectins, C-TypeLigationMaleAntigens, CDAntigens, Differentiation, MyelomonocyticCD68 MoleculeCD68 protein, mouseCX3C Chemokine Receptor 1Cx3cr1 protein, mouseLectins, C-TypeMannose-Binding LectinsMannose ReceptorReceptors, Cell SurfaceReceptors, Chemokinearteriolesblood flow velocitymacrophagesmicrovasculaturemonocytes

Identifiers

PMID24969773
PMCPMC4373588

What OpenQuestion holds

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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.