Evidence map›Paper›PMID 28807010›Full record

ArticleStem cell research & therapy2017

Angiogenic potency evaluation of cell therapy candidates by a novel application of the in vitro aortic ring assay.

Farwah Iqbal, Peter Szaraz, Matthew Librach, Andrée Gauthier-Fisher, Clifford L Librach

Abstract read
In one paragraph

Article in Stem cell research & therapy, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Potency Assay Development: A Keystone for Clinical Use.Advances in experimental medicine and biology · 2023
    Article
  6. Advanced Technologies for Potency Assay Measurement.Advances in experimental medicine and biology · 2023
    Article
  7. Ex Vivo Mouse Aortic Ring Angiogenesis Assay.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. 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

5 authors.

Farwah IqbalThe Create Fertility Centre, 790 Bay Street, Suite 412, Toronto, Ontario, M5G 1N8, Canada. farwah.iqbal@mail.utoronto.ca.
Peter SzarazThe Create Fertility Centre, 790 Bay Street, Suite 412, Toronto, Ontario, M5G 1N8, Canada. peter@createivf.com.
Matthew LibrachThe Create Fertility Centre, 790 Bay Street, Suite 412, Toronto, Ontario, M5G 1N8, Canada.
Andrée Gauthier-FisherThe Create Fertility Centre, 790 Bay Street, Suite 412, Toronto, Ontario, M5G 1N8, Canada.
Clifford L LibrachThe Create Fertility Centre, 790 Bay Street, Suite 412, Toronto, Ontario, M5G 1N8, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDue to limitations of current angiogenesis assays, we aimed to develop a novel application of the rat aortic ring assay to assess the angiogenic potential of mesenchymal stromal cells (MSCs). First-trimester human umbilical cord-derived perivascular cells (FTM HUCPVCs) have multipotent characteristics and previously demonstrated angiogenic potential. We compared the effect of this young source of MSCs and adult bone marrow stromal cells (BMSCs) on ex vivo aortic endothelial network formation.

methodsThoracic segments of adult rat aortas were isolated, sectioned and embedded into Matrigel™. Fluorophore-labeled FTM HUCPVC lines and BMSCs (N = 3) were cocultured with developing endothelial networks (day 0). MSC integration, tube formation and endothelial network growth were monitored daily using phase-contrast and fluorescence microscopy. Quantification of endothelial networks was performed using ImageJ network analysis software on day 5 of coculture.

resultsFTM HUCPVCs from two umbilical cord samples migrated toward and integrated with developing aortic ring tubular networks while displaying elongated morphologies (day 1). In contrast, BMSCs did not show targeted migration and maintained spherical morphologies with limited physical interactions. Within 1 week of coculture, FTM HUCPVC lines contributed to significantly greater radial network growth and network loop formation when compared to BMSCs and untreated networks.

conclusionsWe have developed a novel potency assay to assess the angiogenic potential of cell therapy candidates. Favorable properties of FTM HUCPVCs over BMSCs that we observed with this assay and which merit further study include chemotaxis, affinity for developing vasculature, and physical supportive interactions contributing to the development of endothelial networks.

Indexed as

Cell- and Tissue-Based TherapyNeovascularization, PhysiologicAnimalsAortaBiological AssayCell MovementCell ShapeCoculture TechniquesEndothelial CellsFemaleHumansIn Vitro TechniquesMesenchymal Stem CellsMicroscopy, FluorescencePericytesRats, Sprague-DawleyAngiogenesisAortic ring assayCell migrationCellular regenerative therapyEndothelial networksMesenchymal stromal cellsPerivascular cellsUmbilical cord

Identifiers

PMID28807010
PMCPMC5557530

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Registered trials

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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.