Evidence map›Paper›PMID 27449385›Full record

ArticleJournal of biomedical materials research. Part A2016

Nanofibrillar hydrogel scaffolds from recombinant protein-based polymers with integrin- and proteoglycan-binding domains.

Małgorzata K Włodarczyk-Biegun, Marc W T Werten, Urszula Posadowska, Ingeborg M Storm, Frits A de Wolf, Jeroen J J P van den Beucken, Sander C G Leeuwenburgh, Martien A Cohen Stuart, Marleen Kamperman

Abstract read
In one paragraph

Article in Journal of biomedical materials research. Part A, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

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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

9 authors.

Małgorzata K Włodarczyk-BiegunPhysical Chemistry and Soft Matter, Wageningen University, Stippeneng 4, NL-6708 WE Wageningen, The Netherlands.
Marc W T WertenWageningen UR Food & Biobased Research, Bornse Weilanden 9, NL-6708 WG Wageningen, The Netherlands. marc.werten@wur.nl.
Urszula PosadowskaPhysical Chemistry and Soft Matter, Wageningen University, Stippeneng 4, NL-6708 WE Wageningen, The Netherlands.
Ingeborg M StormPhysical Chemistry and Soft Matter, Wageningen University, Stippeneng 4, NL-6708 WE Wageningen, The Netherlands.
Frits A de WolfWageningen UR Food & Biobased Research, Bornse Weilanden 9, NL-6708 WG Wageningen, The Netherlands.
Jeroen J J P van den BeuckenDepartment of Biomaterials, Radboudumc, Philips Van Leydenlaan 25, NL-6525 EX Nijmegen, The Netherlands.
Sander C G LeeuwenburghDepartment of Biomaterials, Radboudumc, Philips Van Leydenlaan 25, NL-6525 EX Nijmegen, The Netherlands.
Martien A Cohen StuartPhysical Chemistry and Soft Matter, Wageningen University, Stippeneng 4, NL-6708 WE Wageningen, The Netherlands.
Marleen KampermanPhysical Chemistry and Soft Matter, Wageningen University, Stippeneng 4, NL-6708 WE Wageningen, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study describes the design, production, and testing of functionalized variants of a recombinant protein-based polymer that forms nanofibrillar hydrogels with self-healing properties. With a view to bone tissue engineering applications, we equipped these variants with N-terminal extensions containing either (1) integrin-binding (RGD) or (2) less commonly studied proteoglycan-binding (KRSR) cell-adhesive motifs. The polymers were efficiently produced as secreted proteins using the yeast Pichia pastoris and were essentially monodisperse. The pH-responsive protein-based polymers are soluble at low pH and self-assemble into supramolecular fibrils and hydrogels at physiological pH. By mixing functionalized and nonfunctionalized proteins in different ratios, and adjusting pH, hydrogel scaffolds with the same protein concentration but varying content of the two types of cell-adhesive motifs were readily obtained. The scaffolds were used for the two-dimensional culture of MG-63 osteoblastic cells. RGD domains had a slightly stronger effect than KRSR domains on adhesion, activity, and spreading. However, scaffolds featuring both functional domains revealed a clear synergistic effect on cell metabolic activity and spreading, and provided the highest final degree of cell confluency. The mixed functionalized hydrogels presented here thus allowed to tailor the osteoblastic cell response, offering prospects for their further development as scaffolds for bone regeneration. © 2016 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 104A: 3082-3092, 2016.

Indexed as

Binding SitesCell AdhesionCell LineCell SurvivalHumansHydrogel, Polyethylene Glycol DimethacrylateIntegrinsNanofibersOligopeptidesOsteoblastsPichiaProtein BindingProteoglycansRecombinant ProteinsTissue EngineeringTissue Scaffoldsarginyl-glycyl-aspartic acidHydrogel, Polyethylene Glycol DimethacrylateIntegrinslysyl-arginyl-seryl-arginineOligopeptidesProteoglycansRecombinant ProteinsKRSR cell-adhesive domainPichia pastorisprotein-based polymersself-assembled hydrogeltissue engineering

Identifiers

PMID27449385
PMCPMC5129582

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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.