Evidence map›Paper›PMID 31524855›Full record

ArticleJournal of visualized experiments : JoVE2019

Single Cell Durotaxis Assay for Assessing Mechanical Control of Cellular Movement and Related Signaling Events.

Kathryn V Svec, Johnathan B Patterson, Nyla Naim, Alan K Howe

Open access · greenAbstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.3field-weighted citation impact, top 43% of its field
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

6 citing papers in PubMed, 6 citations in OpenAlex.

  1. 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

4 authors at 1 institution in 1 country.

Kathryn V SvecDepartment of Pharmacology, University of Vermont Larner College of Medicine; University of Vermont Cancer Center; Department of Molecular Physiology and Biophysics, University of Vermont Larner College of Medicine.
Johnathan B PattersonDepartment of Pharmacology, University of Vermont Larner College of Medicine; University of Vermont Cancer Center; Department of Molecular Physiology and Biophysics, University of Vermont Larner College of Medicine.
Nyla NaimDepartment of Pharmacology, University of Vermont Larner College of Medicine; University of Vermont Cancer Center; Department of Molecular Physiology and Biophysics, University of Vermont Larner College of Medicine.
Alan K HoweDepartment of Pharmacology, University of Vermont Larner College of Medicine; University of Vermont Cancer Center; Department of Molecular Physiology and Biophysics, University of Vermont Larner College of Medicine; alan.howe@med.uvm.edu.
University of Vermont · US

Funding

Mechano-Chemical Regulation of GPCR/PKA Signaling During Cell MigrationR01GM117490 · NIGMS · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI HOWE, ALAN K · 2016 to 2019
$1.6M
NIGMS NIH HHS R01 GM117490
6 · The paper itself

Abstract

Durotaxis is the process by which cells sense and respond to gradients of tension. In order to study this process in vitro, the stiffness of the substrate underlying a cell must be manipulated. While hydrogels with graded stiffness and long-term migration assays have proven useful in durotaxis studies, immediate, acute responses to local changes in substrate tension allow focused study of individual cell movements and subcellular signaling events. To repeatably test the ability of cells to sense and respond to the underlying substrate stiffness, a modified method for application of acute gradients of increased tension to individual cells cultured on deformable hydrogels is used which allows for real time manipulation of the strength and direction of stiffness gradients imparted upon cells in question. Additionally, by fine tuning the details and parameters of the assay, such as the shape and dimensions of the micropipette or the relative position, placement, and direction of the applied gradient, the assay can be optimized for the study of any mechanically sensitive cell type and system. These parameters can be altered to reliably change the applied stimulus and expand the functionality and versatility of the assay. This method allows examination of both long term durotactic movement as well as more immediate changes in cellular signaling and morphological dynamics in response to changing stiffness.

Indexed as

ChemotaxisSignal TransductionStress, PhysiologicalAnimalsBiosensing TechniquesCell Line, TumorFibroblastsFluorescenceHumansHydrogelsMicrospheresRatsSingle-Cell AnalysisHydrogels

Identifiers

PMID31524855
PMCPMC8162691
OpenAlexW2970521702

What OpenQuestion holds

Textmetadata
LicenceTDM
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.