Evidence map›Paper›PMID 29180787›Full record

ArticleScientific reports2017

Towards the cell-instructive bactericidal substrate: exploring the combination of nanotopographical features and integrin selective synthetic ligands.

Roberta Fraioli, Penelope M Tsimbouri, Leanne E Fisher, Angela H Nobbs, Bo Su, Stefanie Neubauer, Florian Rechenmacher, Horst Kessler, Maria-Pau Ginebra, Matthew J Dalby and 2 more

Abstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. High-Aspect-Ratio Nanostructured Surfaces as Biological Metamaterials.Advanced materials (Deerfield Beach, Fla.) · 2020
    Review
  9. Article
  10. 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

12 authors.

Roberta FraioliBiomaterials, Biomechanics and Tissue Engineering Group, Department of Materials Science and Metallurgical Engineering, Technical University of Catalonia (UPC), Barcelona, 08019, Spain.
Penelope M TsimbouriCentre for Cell Engineering, University of Glasgow, Glasgow, G12, Scotland, UK.
Leanne E FisherBristol Dental School, University of Bristol, Bristol, BS1 2LY, UK.
Angela H NobbsBristol Dental School, University of Bristol, Bristol, BS1 2LY, UK.ORCID 0000-0003-3813-4410
Bo SuBristol Dental School, University of Bristol, Bristol, BS1 2LY, UK.
Stefanie NeubauerInstitute for Advanced Study and Center for Integrated Protein Science, Department Chemie, Technische Universität München, 85748, Garching, Germany.
Florian RechenmacherInstitute for Advanced Study and Center for Integrated Protein Science, Department Chemie, Technische Universität München, 85748, Garching, Germany.
Horst KesslerInstitute for Advanced Study and Center for Integrated Protein Science, Department Chemie, Technische Universität München, 85748, Garching, Germany.ORCID 0000-0002-7292-9789
Maria-Pau GinebraBiomaterials, Biomechanics and Tissue Engineering Group, Department of Materials Science and Metallurgical Engineering, Technical University of Catalonia (UPC), Barcelona, 08019, Spain.
Matthew J DalbyCentre for Cell Engineering, University of Glasgow, Glasgow, G12, Scotland, UK.
José M ManeroBiomaterials, Biomechanics and Tissue Engineering Group, Department of Materials Science and Metallurgical Engineering, Technical University of Catalonia (UPC), Barcelona, 08019, Spain.
Carlos Mas-MorunoBiomaterials, Biomechanics and Tissue Engineering Group, Department of Materials Science and Metallurgical Engineering, Technical University of Catalonia (UPC), Barcelona, 08019, Spain. carles.mas.moruno@upc.edu.ORCID 0000-0001-8337-0872

Funding

Medical Research Council MR/N010345/1
6 · The paper itself

Abstract

Engineering the interface between biomaterials and tissues is important to increase implant lifetime and avoid failures and revision surgeries. Permanent devices should enhance attachment and differentiation of stem cells, responsible for injured tissue repair, and simultaneously discourage bacterial colonization; this represents a major challenge. To take first steps towards such a multifunctional surface we propose merging topographical and biochemical cues on the surface of a clinically relevant material such as titanium. In detail, our strategy combines antibacterial nanotopographical features with integrin selective synthetic ligands that can rescue the adhesive capacity of the surfaces and instruct mesenchymal stem cell (MSC) response. To this end, a smooth substrate and two different high aspect ratio topographies have been produced and coated either with an αvβ3-selective peptidomimetic, an α5β1-selective peptidomimetic, or an RGD/PHSRN peptidic molecule. Results showed that antibacterial effects of the substrates could be maintained when tested on pathogenic Pseudomonas aeruginosa. Further, functionalization increased MSC adhesion to the surfaces and the αvβ3-selective peptidomimetic-coated nanotopographies promoted osteogenesis. Such a dual physicochemical approach to achieve multifunctional surfaces represents a first step in the design of novel cell-instructive biomaterial surfaces.

Indexed as

Anti-Bacterial AgentsBacterial AdhesionBiocompatible MaterialsCell DifferentiationCells, CulturedCoated Materials, BiocompatibleHumansIntegrinsLigandsMesenchymal Stem CellsMicrobial ViabilityOsteogenesisSurface PropertiesTitaniumAnti-Bacterial AgentsBiocompatible MaterialsCoated Materials, BiocompatibleIntegrinsLigandsTitanium

Identifiers

PMID29180787
PMCPMC5703844

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.