Evidence map›Paper›PMID 24626190›Full record

ArticlePloS one2014

Design and construction of an equibiaxial cell stretching system that is improved for biochemical analysis.

Chaitanya Prashant Ursekar, Soo-Kng Teo, Hiroaki Hirata, Ichiro Harada, Keng-Hwee Chiam, Yasuhiro Sawada

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 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Frontiers in bioengineering and biotechnology · 2019
    Review
  10. Article
  11. Article
  12. Article
  13. Biophysical Tools to Study Cellular Mechanotransduction.Bioengineering (Basel, Switzerland) · 2017
    Review
  14. 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

6 authors.

Chaitanya Prashant UrsekarMechanobiology Institute of Singapore, National University of Singapore, Singapore.
Soo-Kng TeoInstitute of High Performance Computing, Agency for Science, Technology and Research, Singapore.
Hiroaki HirataMechanobiology Institute of Singapore, National University of Singapore, Singapore.
Ichiro HaradaLaboratory for Mechanical Medicine, Locomotive Syndrome Research Institute, Nadogaya Hospital, Kashiwa, Chiba, Japan; Graduate School of Bioscience and Biotechnology, Tokyo Institute of Technology, Yokohama, Kanagawa, Japan.
Keng-Hwee ChiamMechanobiology Institute of Singapore, National University of Singapore, Singapore; Bioinformatics Institute, Agency for Science, Technology and Research, Singapore.
Yasuhiro SawadaMechanobiology Institute of Singapore, National University of Singapore, Singapore; Laboratory for Mechanical Medicine, Locomotive Syndrome Research Institute, Nadogaya Hospital, Kashiwa, Chiba, Japan; Department of Biological Sciences, National University of Singapore, Singapore.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We describe the design and validation of an equibiaxial stretching device in which cells are confined to regions of homogeneous strain. Using this device, we seek to overcome a significant limitation of existing equibiaxial stretching devices, in which strains are not homogeneous over the entire region of cell culture. We cast PDMS in a mold to produce a membrane with a cylindrical wall incorporated in the center, which was used to confine cell monolayers to the central membrane region subjected to homogeneous equibiaxial strain. We demonstrated that the presence of the wall to hold the culture medium did not affect strain homogeneity over the majority of the culture surface and also showed that cells adhered well onto the PDMS membranes. We used our device in cyclic strain experiments and demonstrated strain-dependent changes in extracellular signal-regulated kinase (ERK) and tyrosine phosphorylation upon cell stretching. Furthermore, we examined cell responses to very small magnitudes of strain ranging from 1% to 6% and were able to observe a graduated increase in ERK phosphorylation in response to these strains. Collectively, we were able to study cellular biochemical response with a high degree of accuracy and sensitivity to fine changes in substrate strain. Because we have designed our device along the lines of existing equibiaxial stretching technologies, we believe that our innovations can be incorporated into existing systems. This device would provide a useful addition to the set of tools applied for in vitro studies of cell mechanobiology.

Indexed as

Stress, MechanicalAlgorithmsAluminumAnimalsAnisotropyBiocompatible MaterialsCells, CulturedCollagenCytological TechniquesDimethylpolysiloxanesExtracellular Signal-Regulated MAP KinasesFinite Element AnalysisHEK293 CellsHumansMaterials TestingMembranes, ArtificialAluminumbaysilonBiocompatible MaterialsCollagenDimethylpolysiloxanesExtracellular Signal-Regulated MAP KinasesMembranes, ArtificialTyrosine

Identifiers

PMID24626190
PMCPMC3953117

What OpenQuestion holds

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LicenceCC BY
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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.