Evidence map›Paper›PMID 25329487›Full record

ArticlePloS one2014

Guidance of mesenchymal stem cells on fibronectin structured hydrogel films.

Annika Kasten, Tamara Naser, Kristina Brüllhoff, Jörg Fiedler, Petra Müller, Martin Möller, Joachim Rychly, Jürgen Groll, Rolf E Brenner

Abstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. 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

9 authors.

Annika KastenLaboratory of Cell Biology, Rostock University Medical Center, Rostock, Germany.
Tamara NaserDivision for Biochemistry of Joint and Connective Tissue Diseases of the Orthopedic Department, University of Ulm, Ulm, Germany.
Kristina BrüllhoffDWI Leibniz Institute for Interactive Materials and Institute of Technical and Macromolecular Chemistry, RWTH Aachen University, Aachen, Germany.
Jörg FiedlerDivision for Biochemistry of Joint and Connective Tissue Diseases of the Orthopedic Department, University of Ulm, Ulm, Germany.
Petra MüllerLaboratory of Cell Biology, Rostock University Medical Center, Rostock, Germany.
Martin MöllerDWI Leibniz Institute for Interactive Materials and Institute of Technical and Macromolecular Chemistry, RWTH Aachen University, Aachen, Germany.
Joachim RychlyLaboratory of Cell Biology, Rostock University Medical Center, Rostock, Germany.
Jürgen GrollDWI Leibniz Institute for Interactive Materials and Institute of Technical and Macromolecular Chemistry, RWTH Aachen University, Aachen, Germany; Department and Chair of Functional Materials in Medicine and Dentistry, University of Würzburg, Würzburg, Germany.
Rolf E BrennerDivision for Biochemistry of Joint and Connective Tissue Diseases of the Orthopedic Department, University of Ulm, Ulm, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Designing of implant surfaces using a suitable ligand for cell adhesion to stimulate specific biological responses of stem cells will boost the application of regenerative implants. For example, materials that facilitate rapid and guided migration of stem cells would promote tissue regeneration. When seeded on fibronectin (FN) that was homogeneously immmobilized to NCO-sP(EO-stat-PO), which otherwise prevents protein binding and cell adhesion, human mesenchymal stem cells (MSC) revealed a faster migration, increased spreading and a more rapid organization of different cellular components for cell adhesion on fibronectin than on a glass surface. To further explore, how a structural organization of FN controls the behavior of MSC, adhesive lines of FN with varying width between 10 µm and 80 µm and spacings between 5 µm and 20 µm that did not allow cell adhesion were generated. In dependance on both line width and gaps, cells formed adjacent cell contacts, were individually organized in lines, or bridged the lines. With decreasing sizes of FN lines, speed and directionality of cell migration increased, which correlated with organization of the actin cytoskeleton, size and shape of the nuclei as well as of focal adhesions. Together, defined FN lines and gaps enabled a fine tuning of the structural organization of cellular components and migration. Microstructured adhesive substrates can mimic the extracellular matrix in vivo and stimulate cellular mechanisms which play a role in tissue regeneration.

Indexed as

RegenerationActinsCell AdhesionCell LineCell MovementCytoskeletonExtracellular MatrixFibronectinsHumansLigandsMesenchymal Stem CellsActinsFibronectinsLigands

Identifiers

PMID25329487
PMCPMC4198140

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.