Evidence map›Paper›PMID 22374788›Full record

ArticleJournal of biomedical materials research. Part A2012

Differential effects of substrate modulus on human vascular endothelial, smooth muscle, and fibroblastic cells.

Karyn G Robinson, Ting Nie, Aaron D Baldwin, Elaine C Yang, Kristi L Kiick, Robert E Akins

Open access · greenAbstract read
In one paragraph

Article in Journal of biomedical materials research. Part A, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.9field-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

25 citing papers in PubMed, 48 citations in OpenAlex.

  1. Article
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  5. Review
  6. Quantification of uncertainty in a new network model of pulmonary arterial adventitial fibroblast pro-fibrotic signalling.Philosophical transactions. Series A, Mathematical, physical, and engineering sciences · 2020
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  19. Review
  20. Nylon-3 polymers that enable selective culture of endothelial cells.Journal of the American Chemical Society · 2013
    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 at 4 institutions in 1 country.

Karyn G RobinsonTissue Engineering and Regenerative Medicine Laboratory, Nemours Biomedical Research, Alfred I. duPont Hospital for Children, Wilmington, Delaware 19803, USA.
Ting Nie
Aaron D Baldwin
Elaine C Yang
Kristi L Kiick
Robert E Akins
Alfred I. duPont Hospital for Children · USDuPont (United States) · USBiotechnology Institute · USUniversity of Delaware · US

Funding

Predictive Modeling & Optimal Control Framework for Model-Based Epidemic Response in DelawareP20GM103446 · NIGMS · UNIVERSITY OF DELAWARE · PI Anjana Narayan Bhat · 2012 to 2026
$67.2M
VOLUMETRIC BREAST DENSITY ESTIMATION USING BREAST SURFACE RECONSTRUCTEDP20RR016472 · NCRR · UNIVERSITY OF DELAWARE · PI STEINER, KARL V. · 2001 to 2011
$37.6M
UDE COBRE: STRAINED MOLECULES FOR SYNTHESIS OF UNNATURAL AMINO ACIDSP20RR017716 · NCRR · UNIVERSITY OF DELAWARE · PI BEEBE, THOMAS PAUL · 2002 to 2011
$16.9M
TRAJECTORIES OF CHANGE IN BMI STATUS IN EARLY CHILDHOODP20RR020173 · NCRR · NEMOURS CHILDREN'S HOSPITAL, DELAWARE · PI MASON, ROBERT · 2004 to 2011
$14.9M
Center for Pediatric ResearchP20GM103464 · NIGMS · NEMOURS CHILDREN'S HOSPITAL, DELAWARE · PI SHAFFER, THOMAS H · 2012 to 2014
$5.6M
Nanoscale engineering of novel erodible drug delivery matricesR01EB003172 · NIBIB · UNIVERSITY OF DELAWARE · PI FURST, ERIC M · 2003 to 2006
$1.2M
NCRR NIH HHS P20 RR016472NCRR NIH HHS P20-RR016472NCRR NIH HHS P20 RR017716NCRR NIH HHS P20-RR017716NCRR NIH HHS P20-RR020173NIBIB NIH HHS R01 EB003172NIGMS NIH HHS P20 GM103446NIGMS NIH HHS P20 GM103464
6 · The paper itself

Abstract

Regenerative medicine approaches offer attractive alternatives to standard vascular reconstruction; however, the biomaterials to be used must have optimal biochemical and mechanical properties. To evaluate the effects of biomaterial properties on vascular cells, heparinized poly(ethylene glycol) (PEG)-based hydrogels of three different moduli, 13.7, 5.2, and 0.3 kPa, containing fibronectin and growth factor were utilized to support the growth of three human vascular cell types. The cell types exhibited differences in attachment, proliferation, and gene expression profiles associated with the hydrogel modulus. Human vascular smooth muscle cells demonstrated preferential attachment on the highest-modulus hydrogel, adventitial fibroblasts demonstrated preferential growth on the highest-modulus hydrogel, and human umbilical vein endothelial cells demonstrated preferential growth on the lowest-modulus hydrogel investigated. Our studies suggest that the growth of multiple vascular cell types can be supported by PEG hydrogels and that different populations can be controlled by altering the mechanical properties of biomaterials.

Indexed as

AnimalsCell AdhesionCell ProliferationCell ShapeCluster AnalysisElastic ModulusFibroblastsGene Expression RegulationHumansHuman Umbilical Vein Endothelial CellsHydrogel, Polyethylene Glycol DimethacrylateMiceMuscle, Smooth, VascularMyocytes, Smooth MuscleNIH 3T3 CellsOscillometryHydrogel, Polyethylene Glycol Dimethacrylate

Identifiers

PMID22374788
PMCPMC3351091
OpenAlexW1989740708

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.