Evidence map›Paper›PMID 24281642›Full record

ArticlePlastic and reconstructive surgery2013

Vascular smooth muscle cell optimization of vasculogenesis within naturally derived, biodegradable, hybrid hydrogel scaffolds.

Alyssa Reiffel Golas, Justin L Perez, Natalia Fullerton, Nikola Lekic, Rachel Campbell Hooper, Jason A Spector

Abstract read
In one paragraph

Article in Plastic and reconstructive surgery, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.5field-weighted citation impact, top 32% 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

0 citing papers in PubMed, 7 citations in OpenAlex.

No citing paper in PubMed yet.

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 1 institution in 2 countries.

Alyssa Reiffel GolasNew York, N.Y. From the Laboratory of Bioregenerative Medicine and Surgery, Division of Plastic Surgery, Weill Cornell Medical College.
Justin L Perez
Natalia Fullerton
Nikola Lekic
Rachel Campbell Hooper
Jason A Spector
Cornell University · US

Funding

Multidisciplinary Vascular Surgery Research Training ProgramT32HL083824 · NHLBI · WEILL MEDICAL COLL OF CORNELL UNIV · PI EVANS, TODD R · 2006 to 2010
$791k
Clinical and Translational Science Center (TL1)TL1RR024998 · NCRR · WEILL MEDICAL COLL OF CORNELL UNIV · PI IMPERATO-MCGINLEY, JULIANNE L · 2007 to 2011
$695k
Clinical and Translational Science CenterTL1TR000459 · NCATS · WEILL MEDICAL COLL OF CORNELL UNIV · PI IMPERATO-MCGINLEY, JULIANNE L · 2012 to 2016
$451k
NCATS NIH HHS TL1 TR000459NCRR NIH HHS TL1 RR024998NHLBI NIH HHS T32 HL083824NHLBI NIH HHS T32 HL083824-05
6 · The paper itself

Abstract

backgroundAs vascularization represents the rate-limiting step in permanent incorporation of hydrogel-based tissue-regeneration templates, the authors sought to identify the material chemistry that would optimize endothelial cell adhesion and invasion into custom hydrogel constructs. The authors further investigated induction of endothelial tubule formation by growth factor supplementation and paracrine stimulation.

methodsHydrogel scaffolds consisting of combinations of alginate, collagen type I, and chitosan were seeded with human umbilical vein endothelial cells and maintained under standard conditions for 14 days. Cell density and invasion were then evaluated. Tubule formation was evaluated following basic fibroblast growth factor addition or co-culture with human aortic smooth muscle cells.

resultsHuman umbilical vein endothelial cells demonstrated greatest cell-surface density and invasion volumes with alginate and collagen (10:1 weight/weight) scaffolds (p < 0.05). Supplementation with basic fibroblast growth factor increased surface density but neither invasion nor tubule formation. A significant increase in tubule content/organization was observed with increasing human aortic smooth muscle cell-to-human umbilical vein endothelial cell ratio co-culture.

conclusionsAlginate and collagen 10:1 scaffolds allow for maximal cellularization compared with other combinations studied. Growth factor supplementation did not affect human umbilical vein endothelial cell invasion or morphology. Paracrine signaling by means of co-culture with human umbilical vein endothelial cells stimulated endothelial tubule formation and vascular protonetwork organization. These findings serve to guide future endeavors toward fabrication of prevascularized tissue constructs.

Indexed as

Neovascularization, PhysiologicTissue ScaffoldsAlginatesBiocompatible MaterialsCell AdhesionChitosanCoculture TechniquesCollagen Type IEndothelial CellsFibroblast Growth Factor 2HumansHuman Umbilical Vein Endothelial CellsHydrogel, Polyethylene Glycol DimethacrylateImmunoglobulin GMelphalanMuscle, Smooth, VascularAlginatesantineoplastic agent K 18arginyl-glycyl-aspartic acidBiocompatible MaterialsChitosanCollagen Type IFibroblast Growth Factor 2Hydrogel, Polyethylene Glycol DimethacrylateImmunoglobulin GMelphalanOligopeptides

Identifiers

PMID24281642
PMCPMC3843154
OpenAlexW2087986630

What OpenQuestion holds

Textmetadata
LicenceTDM
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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.