Evidence map›Paper›PMID 25795217›Full record

ArticleAngiogenesis2015

Large-scale time series microscopy of neovessel growth during angiogenesis.

Urs Utzinger, Brenda Baggett, Jeffrey A Weiss, James B Hoying, Lowell T Edgar

Open access · greenAbstract read
In one paragraph

Article in Angiogenesis, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

47 citing papers in PubMed, 108 citations in OpenAlex.

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  19. Vascularized Tissue Organoids.Bioengineering (Basel, Switzerland) · 2023
    Review
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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

5 authors at 3 institutions in 1 country.

Urs UtzingerDepartment of Biomedical Engineering, University of Arizona, Tucson, AZ, USA, utzinger@email.arizona.edu.
Brenda Baggett
Jeffrey A Weiss
James B Hoying
Lowell T Edgar
University of Arizona · USUniversity of Utah · USUniversity of Louisville Hospital · US

Funding

Angiogenesis and the Extracellular MatrixR01HL077683 · NHLBI · UNIVERSITY OF UTAH · PI WEISS, JEFFREY A. · 2004 to 2011
$3.8M
Fluorender: An Imaging Tool for Visualization and Analysis of Confocal Data as ApR01GM098151 · NIGMS · UNIVERSITY OF UTAH · PI HANSEN, CHARLES · 2011 to 2014
$1.2M
Advanced Intravital MicroscopeS10RR023737 · NCRR · UNIVERSITY OF ARIZONA · PI UTZINGER, URS · 2007 to 2007
$458k
NCRR NIH HHS S10 RR023737NCRR NIH HHS S10RR023737NHLBI NIH HHS R01 HL077683NHLBI NIH HHS R01HL077683NIGMS NIH HHS R01 GM098151
6 · The paper itself

Abstract

During angiogenesis, growing neovessels must effectively navigate through the tissue space as they elongate and subsequently integrate into a microvascular network. While time series microscopy has provided insight into the cell activities within single growing neovessel sprouts, less is known concerning neovascular dynamics within a large angiogenic tissue bed. Here, we developed a time-lapse imaging technique that allowed visualization and quantification of sprouting neovessels as they form and grow away from adult parent microvessels in three dimensions over cubic millimeters of matrix volume during the course of up to 5 days on the microscope. Using a new image acquisition procedure and novel morphometric analysis tools, we quantified the elongation dynamics of growing neovessels and found an episodic growth pattern accompanied by fluctuations in neovessel diameter. Average elongation rate was 5 μm/h for individual vessels, but we also observed considerable dynamic variability in growth character including retraction and complete regression of entire neovessels. We observed neovessel-to-neovessel directed growth over tens to hundreds of microns preceding tip-to-tip inosculation. As we have previously described via static 3D imaging at discrete time points, we identified different collagen fibril structures associated with the growing neovessel tip and stalk, and observed the coordinated alignment of growing neovessels in a deforming matrix. Overall analysis of the entire image volumes demonstrated that although individual neovessels exhibited episodic growth and regression, there was a monotonic increase in parameters associated with the entire vascular bed such as total network length and number of branch points. This new time-lapse imaging approach corroborated morphometric changes in individual neovessels described by us and others, as well as captured dynamic neovessel behaviors unique to days-long angiogenesis within the forming neovascular network.

Indexed as

Neovascularization, PhysiologicAnimalsAnisotropyCell Culture TechniquesCollagenEpididymisExtracellular MatrixGreen Fluorescent ProteinsHumansImage Processing, Computer-AssistedImaging, Three-DimensionalMaleMicroscopyMicrovesselsMorphogenesisRatsCollagenGreen Fluorescent ProteinsVascular Endothelial Growth Factor A

Identifiers

PMID25795217
PMCPMC4782613
OpenAlexW2016701600

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.