Evidence map›Paper›PMID 25687334›Full record

ArticleExperimental biology and medicine (Maywood, N.J.)2015

Temporal responses of human endothelial and smooth muscle cells exposed to uniaxial cyclic tensile strain.

Alexandra M Greiner, Sarah A Biela, Hao Chen, Joachim P Spatz, Ralf Kemkemer

Open access · greenAbstract read
In one paragraph

Article in Experimental biology and medicine (Maywood, N.J.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

11 citing papers in PubMed, 22 citations in OpenAlex.

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  9. Tissue engineering. Part C, Methods · 2019
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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

5 authors at 2 institutions in 1 country.

Alexandra M GreinerDepartment of Cell- and Neurobiology, Karlsruhe Institute of Technology (KIT), 76131 Karlsruhe, Germany.
Sarah A BielaDepartment of New Materials and Biosystems, Max Planck Institute for Intelligent Systems, 70569 Stuttgart, Germany.
Hao ChenDepartment of Cell- and Neurobiology, Karlsruhe Institute of Technology (KIT), 76131 Karlsruhe, Germany.
Joachim P SpatzDepartment of New Materials and Biosystems, Max Planck Institute for Intelligent Systems, 70569 Stuttgart, Germany Department of Biophysical Chemistry, University of Heidelberg, 69120 Heidelberg, Germany.
Ralf KemkemerDepartment of New Materials and Biosystems, Max Planck Institute for Intelligent Systems, 70569 Stuttgart, Germany Department of Applied Chemistry, Reutlingen University, 72762 Reutlingen, Germany ralf.kemkemer@reutlingen-university.de.
Max Planck Institute for Intelligent Systems · DEKarlsruhe Institute of Technology · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The physiology of vascular cells depends on stimulating mechanical forces caused by pulsatile flow. Thus, mechano-transduction processes and responses of primary human endothelial cells (ECs) and smooth muscle cells (SMCs) have been studied to reveal cell-type specific differences which may contribute to vascular tissue integrity. Here, we investigate the dynamic reorientation response of ECs and SMCs cultured on elastic membranes over a range of stretch frequencies from 0.01 to 1 Hz. ECs and SMCs show different cell shape adaptation responses (reorientation) dependent on the frequency. ECs reveal a specific threshold frequency (0.01 Hz) below which no responses is detectable while the threshold frequency for SMCs could not be determined and is speculated to be above 1 Hz. Interestingly, the reorganization of the actin cytoskeleton and focal adhesions system, as well as changes in the focal adhesion area, can be observed for both cell types and is dependent on the frequency. RhoA and Rac1 activities are increased for ECs but not for SMCs upon application of a uniaxial cyclic tensile strain. Analysis of membrane protrusions revealed that the spatial protrusion activity of ECs and SMCs is independent of the application of a uniaxial cyclic tensile strain of 1 Hz while the total number of protrusions is increased for ECs only. Our study indicates differences in the reorientation response and the reaction times of the two cell types in dependence of the stretching frequency, with matching data for actin cytoskeleton, focal adhesion realignment, RhoA/Rac1 activities, and membrane protrusion activity. These are promising results which may allow cell-type specific activation of vascular cells by frequency-selective mechanical stretching. This specific activation of different vascular cell types might be helpful in improving strategies in regenerative medicine.

Indexed as

Tensile StrengthActin CytoskeletonCell ShapeEndothelial CellsFocal AdhesionsHumansMechanotransduction, CellularMyocytes, Smooth MusclePulsatile Flowrac1 GTP-Binding ProteinrhoA GTP-Binding Proteinrac1 GTP-Binding ProteinrhoA GTP-Binding Proteinactinendothelial cellfocal adhesionRho GTPasesSmooth muscle celluniaxial cyclic tensile strain

Identifiers

PMID25687334
PMCPMC4935260
OpenAlexW2012664310

What OpenQuestion holds

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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.