Evidence map›Paper›PMID 36189808›Full record

ArticlePhilosophical transactions of the Royal Society of London. Series B, Biological sciences2022

Simultaneous assessment of radial and axial myocyte mechanics by combining atomic force microscopy and carbon fibre techniques.

Rémi Peyronnet, Aesha Desai, Jan-Christoph Edelmann, Breanne A Cameron, Ramona Emig, Peter Kohl, Delphine Dean

Open access · greenAbstract read
In one paragraph

Article in Philosophical transactions of the Royal Society of London. Series B, Biological sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.3field-weighted citation impact, top 23% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

  1. Cardiac myofibril networks induce shear stress.NPJ systems biology and applications · 2026
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  7. Simultaneous assessment of radial and axial myocyte mechanics by combining atomic force microscopy and carbon fibre techniques.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2022
    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

7 authors at 3 institutions in 3 countries.

Rémi PeyronnetInstitute for Experimental Cardiovascular Medicine, University Heart Center Freiburg - Bad Krozingen, University of Freiburg, 79110 Freiburg, Germany.ORCID 0000-0002-5708-6410
Aesha DesaiClemson University, Clemson, SC, USA.
Jan-Christoph EdelmannNational Heart and Lung Institute, Imperial College London, London, UK.
Breanne A CameronInstitute for Experimental Cardiovascular Medicine, University Heart Center Freiburg - Bad Krozingen, University of Freiburg, 79110 Freiburg, Germany.
Ramona EmigInstitute for Experimental Cardiovascular Medicine, University Heart Center Freiburg - Bad Krozingen, University of Freiburg, 79110 Freiburg, Germany.ORCID 0000-0003-1832-6976
Peter KohlInstitute for Experimental Cardiovascular Medicine, University Heart Center Freiburg - Bad Krozingen, University of Freiburg, 79110 Freiburg, Germany.
Delphine DeanClemson University, Clemson, SC, USA.ORCID 0000-0002-8631-2640
University of Freiburg · DEClemson University · USImperial College London · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cardiomyocytes sense and shape their mechanical environment, contributing to its dynamics by their passive and active mechanical properties. While axial forces generated by contracting cardiomyocytes have been amply investigated, the corresponding radial mechanics remain poorly characterized. Our aim is to simultaneously monitor passive and active forces, both axially and radially, in cardiomyocytes freshly isolated from adult mouse ventricles. To do so, we combine a carbon fibre (CF) set-up with a custom-made atomic force microscope (AFM). CF allows us to apply stretch and to record passive and active forces in the axial direction. The AFM, modified for frontal access to fit in CF, is used to characterize radial cell mechanics. We show that stretch increases the radial elastic modulus of cardiomyocytes. We further find that during contraction, cardiomyocytes generate radial forces that are reduced, but not abolished, when cells are forced to contract near isometrically. Radial forces may contribute to ventricular wall thickening during contraction, together with the dynamic re-orientation of cells and sheetlets in the myocardium. This new approach for characterizing cell mechanics allows one to obtain a more detailed picture of the balance of axial and radial mechanics in cardiomyocytes at rest, during stretch, and during contraction. This article is part of the theme issue 'The cardiomyocyte: new revelations on the interplay between architecture and function in growth, health, and disease'.

Indexed as

Myocytes, CardiacAnimalsCarbon FiberMiceMicroscopy, Atomic ForceCarbon Fiberactive forcesAFMcardiomyocyteselastic modulusstiffnessstretch

Identifiers

PMID36189808
PMCPMC9527909
OpenAlexW4300687914

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.