Evidence map›Paper›PMID 27391047›Full record

ArticleACS nano2016

Protein Adsorption as a Key Mediator in the Nanotopographical Control of Cell Behavior.

Elie Ngandu Mpoyi, Marco Cantini, Paul M Reynolds, Nikolaj Gadegaard, Matthew J Dalby, Manuel Salmerón-Sánchez

Abstract read
In one paragraph

Article in ACS nano, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing 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

33 citing papers in PubMed.

  1. Review
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  13. TiOACS applied materials & interfaces · 2022
    Article
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  19. Stem Cell Niche Microenvironment: Review.Bioengineering (Basel, Switzerland) · 2021
    Review
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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

6 authors.

Elie Ngandu MpoyiDivision of Biomedical Engineering, School of Engineering, University of Glasgow , Glasgow G12 8LT, United Kingdom.
Marco CantiniDivision of Biomedical Engineering, School of Engineering, University of Glasgow , Glasgow G12 8LT, United Kingdom.
Paul M ReynoldsDivision of Biomedical Engineering, School of Engineering, University of Glasgow , Glasgow G12 8LT, United Kingdom.
Nikolaj GadegaardDivision of Biomedical Engineering, School of Engineering, University of Glasgow , Glasgow G12 8LT, United Kingdom.
Matthew J DalbyCenter for Cell Engineering, Institute of Molecular Cell and Systems Biology, University of Glasgow , Joseph Black Building, University Avenue, Glasgow G12 8QQ, United Kingdom.
Manuel Salmerón-SánchezDivision of Biomedical Engineering, School of Engineering, University of Glasgow , Glasgow G12 8LT, United Kingdom.

Funding

Biotechnology and Biological Sciences Research Council BB/G008868/1Biotechnology and Biological Sciences Research Council JF20604Medical Research Council MR/L022710/1
6 · The paper itself

Abstract

Surface nanotopography is widely employed to control cell behavior and in particular controlled disorder has been shown to be important in cell differentiation/maturation. However, extracellular matrix proteins, such as fibronectin (FN), initially adsorbed on a biomaterial surface are known to mediate the interaction of synthetic materials with cells. In this work, we examine the effect of nanotopography on cell behavior through this adsorbed layer of adhesive proteins using a nanostructured polycarbonate surface comprising 150 nm-diameter pits originally defined using electron beam lithography. We address the effect of this nanopitted surface on FN adsorption and subsequently on cell morphology and behavior using C2C12 myoblasts. Wettability measurements and atomic force microscopy imaging showed that protein is adsorbed both within the interpits spaces and inside the nanopits. Cells responded to this coated nanotopography with the formation of fewer but larger focal adhesions and by mimicking the pit patterns within their cytoskeleton, nanoimprinting, ultimately achieving higher levels of myogenic differentiation compared to a flat control. Both focal adhesion assembly and nanoimprinting were found to be dependent on cell contractility and are adversely affected by the use of blebbistatin. Our results demonstrate the central role of the nanoscale protein interface in mediating cell-nanotopographical interactions and implicate this interface as helping control the mechanotransductive cascade.

Indexed as

Cell AdhesionFibronectinsNanostructuresAdsorptionFocal AdhesionsMicroscopy, Atomic ForceProteinsSurface PropertiesFibronectinsProteinsbiomaterialscellular responsefibronectinnanotopographyprotein adsorption

Identifiers

PMID27391047
PMCPMC4980054

What OpenQuestion holds

Textmetadata
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.