Evidence map›Paper›PMID 32201175›Full record

ArticleJournal of molecular and cellular cardiology2020

Intact myocardial preparations reveal intrinsic transmural heterogeneity in cardiac mechanics.

Fotios G Pitoulis, Waseem Hasan, Mary Papadaki, Nicolas G Clavere, Filippo Perbellini, Sian E Harding, Jonathan A Kirk, Samuel Y Boateng, Pieter P de Tombe, Cesare M Terracciano

Open access · hybridAbstract read
In one paragraph

Article in Journal of molecular and cellular cardiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.6field-weighted citation impact, top 19% 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

22 citing papers in PubMed, 22 citations in OpenAlex.

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  20. Regional differences in arrhythmogenesis.The Journal of general physiology · 2021
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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

10 authors at 4 institutions in 3 countries.

Fotios G PitoulisNational Heart and Lung Institute, Imperial College London, UK.
Waseem HasanNational Heart and Lung Institute, Imperial College London, UK.
Mary PapadakiDepartment of Cell and Molecular Physiology, Loyola University Chicago, USA.
Nicolas G ClavereSchool of Biological Sciences, University of Reading, UK.
Filippo PerbelliniNational Heart and Lung Institute, Imperial College London, UK; Institute for Molecular and Translational Therapeutic Strategies, Hannover Medical School, DE, Germany.
Sian E HardingNational Heart and Lung Institute, Imperial College London, UK.
Jonathan A KirkDepartment of Cell and Molecular Physiology, Loyola University Chicago, USA.
Samuel Y BoatengSchool of Biological Sciences, University of Reading, UK.
Pieter P de TombeNational Heart and Lung Institute, Imperial College London, UK; Department of Cell and Molecular Physiology, Loyola University Chicago, USA.
Cesare M TerraccianoNational Heart and Lung Institute, Imperial College London, UK. Electronic address: c.terracciano@imperial.ac.uk.
Imperial College London · GBLoyola University Chicago · USUniversity of Reading · GBMedizinische Hochschule Hannover · DE

Funding

GSK-3β Localizes to the Myofilament and Modifies its Function in Ischemic CardiomyopathyR01HL136737 · NHLBI · UNIVERSITY OF CHICAGO · PI JONATHAN A KIRK · 2017 to 2026
$4.5M
British Heart Foundation FS/18/37/33642NHLBI NIH HHS R01 HL136737
6 · The paper itself

Abstract

Determining transmural mechanical properties in the heart provides a foundation to understand physiological and pathophysiological cardiac mechanics. Although work on mechanical characterisation has begun in isolated cells and permeabilised samples, the mechanical profile of living individual cardiac layers has not been examined. Myocardial slices are 300 μm-thin sections of heart tissue with preserved cellular stoichiometry, extracellular matrix, and structural architecture. This allows for cardiac mechanics assays in the context of an intact in vitro organotypic preparation. In slices obtained from the subendocardium, midmyocardium and subepicardium of rats, a distinct pattern in transmural contractility is found that is different from that observed in other models. Slices from the epicardium and midmyocardium had a higher active tension and passive tension than the endocardium upon stretch. Differences in total myocyte area coverage, and aspect ratio between layers underlined the functional readouts, while no differences were found in total sarcomeric protein and phosphoprotein between layers. Such intrinsic heterogeneity may orchestrate the normal pumping of the heart in the presence of transmural strain and sarcomere length gradients in the in vivo heart.

Indexed as

AnimalsBiomechanical PhenomenaCarrier ProteinsMyocardiumMyosin Binding Protein CMyosin Light ChainsPhosphorylationRats, Sprague-DawleySarcomeresTroponinCarrier ProteinsMyosin Binding Protein CMyosin Light ChainsTroponinCardiac mechanicsContractilityExtracellular matrixIntact tissueSarcomeric apparatusTransmurality

Identifiers

PMID32201175
PMCPMC7246333
OpenAlexW3011334072

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.