Evidence map›Paper›PMID 27042236›Full record

ArticleCellular and molecular bioengineering2016

Poly(ethylene glycol) Hydrogel Scaffolds Containing Cell-Adhesive and Protease-Sensitive Peptides Support Microvessel Formation by Endothelial Progenitor Cells.

Erica B Peters, Nicolas Christoforou, Kam W Leong, George A Truskey, Jennifer L West

Open access · greenAbstract read
In one paragraph

Article in Cellular and molecular bioengineering, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

37 citing papers in PubMed, 71 citations in OpenAlex.

  1. Biofabrication and Characterization of Vascularizing PEG-Norbornene Microgels.Journal of biomedical materials research. Part A · 2025
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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 1 institution in 1 country.

Erica B PetersFitzpatrick CIEMAS Building, Room 1427, Box 90281, Duke University, Department of Biomedical Engineering, Durham, NC 27708.
Nicolas ChristoforouP.O. Box 127788, Khalifa University, Department of Biomedical Engineering, Abu Dhabi, UAE.
Kam W Leong1210 Amsterdam Avenue, Mail Code 8904, Columbia University, Department of Biomedical Engineering, New York, NY 10027.
George A TruskeyFitzpatrick CIEMAS Building, Room 1427, Box 90281, Duke University, Department of Biomedical Engineering, Durham, NC 27708.
Jennifer L WestFitzpatrick CIEMAS Building, Room 1427, Box 90281, Duke University, Department of Biomedical Engineering, Durham, NC 27708.
Duke University · US

Funding

Fabrication, perfusion and imaging of pre-vascularized tissue scaffoldsR01HL097520 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI DICKINSON, MARY E, WEST, JENNIFER L · 2010 to 2013
$1.9M
NHLBI NIH HHS R01 HL097520
6 · The paper itself

Abstract

The development of stable, functional microvessels remains an important obstacle to overcome for tissue engineered organs and treatment of ischemia. Endothelial progenitor cells (EPCs) are a promising cell source for vascular tissue engineering as they are readily obtainable and carry the potential to differentiate towards all endothelial phenotypes. The aim of this study was to investigate the ability of human umbilical cord blood-derived EPCs to form vessel-like structures within a tissue engineering scaffold material, a cell-adhesive and proteolytically degradable poly(ethylene glycol) (PEG) hydrogel. EPCs in co-culture with angiogenic mural cells were encapsulated in hydrogel scaffolds by mixing with polymeric precursors and using a mild photocrosslinking process to form hydrogels with homogeneously dispersed cells. EPCs formed 3D microvessels networks that were stable for at least 30 days in culture, without the need for supplemental angiogenic growth factors. These 3D EPC microvessels displayed aspects of physiological microvasculature with lumen formation, expression of endothelial cell proteins (connexin 32, VE-cadherin, eNOS), basement membrane formation with collagen IV and laminin, perivascular investment of PDGFR-β and α-SMA positive cells, and EPC quiescence (<1% proliferating cells) by 2 weeks of co-culture. Our findings demonstrate the development of a novel, reductionist system that is well-defined and reproducible for studying progenitor cell-driven microvessel formation.

Identifiers

PMID27042236
PMCPMC4812433
OpenAlexW1760250980

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.