Evidence map›Paper›PMID 26085516›Full record

ArticleOpen biology2015

Crosstalk of cardiomyocytes and fibroblasts in co-cultures.

J Rother, C Richter, L Turco, F Knoch, I Mey, S Luther, A Janshoff, E Bodenschatz, M Tarantola

Abstract read
In one paragraph

Article in Open biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing 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

28 citing papers in PubMed.

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  9. Improving Right Ventricular Function by Increasing BMP Signaling with FK506.American journal of respiratory cell and molecular biology · 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

9 authors.

J RotherInstitute of Physical Chemistry, University of Goettingen, Tammannstrasse 6, Goettingen 37077, Germany.
C RichterResearch Group Biomedical Physics, Max Planck Institute for Dynamics and Self-Organization (MPIDS), Am Fassberg 17, Goettingen 37077, Germany Heart Research Center Goettingen, Robert-Koch-Strasse 40, Goettingen 37099, Germany.
L TurcoLaboratory for Fluid Dynamics, Pattern Formation and Biocomplexity, Am Fassberg 17, Goettingen 37077, Germany.
F KnochLaboratory for Fluid Dynamics, Pattern Formation and Biocomplexity, Am Fassberg 17, Goettingen 37077, Germany.
I MeyInstitute of Organic and Biomolecular Chemistry, Georg-August University, Tammannstrasse 6, Goettingen 37077, Germany.
S LutherResearch Group Biomedical Physics, Max Planck Institute for Dynamics and Self-Organization (MPIDS), Am Fassberg 17, Goettingen 37077, Germany German Center for Cardiovascular Research (DZHK), Oudenarder Strasse 16, Berlin 13347, Germany Heart Research Center Goettingen, Robert-Koch-Strasse 40, Goettingen 37099, Germany Institute of Nonlinear Dynamics, Georg-August University, Friedrich-Hund-Platz 1, Goettingen 37077, Germany.
A JanshoffInstitute of Physical Chemistry, University of Goettingen, Tammannstrasse 6, Goettingen 37077, Germany.
E BodenschatzLaboratory for Fluid Dynamics, Pattern Formation and Biocomplexity, Am Fassberg 17, Goettingen 37077, Germany German Center for Cardiovascular Research (DZHK), Oudenarder Strasse 16, Berlin 13347, Germany Heart Research Center Goettingen, Robert-Koch-Strasse 40, Goettingen 37099, Germany Institute of Nonlinear Dynamics, Georg-August University, Friedrich-Hund-Platz 1, Goettingen 37077, Germany.
M TarantolaLaboratory for Fluid Dynamics, Pattern Formation and Biocomplexity, Am Fassberg 17, Goettingen 37077, Germany marco.tarantola@ds.mpg.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Electromechanical function of cardiac muscle depends critically on the crosstalk of myocytes with non-myocytes. Upon cardiac fibrosis, fibroblasts translocate into infarcted necrotic tissue and alter their communication capabilities. In the present in vitro study, we determined a multiple parameter space relevant for fibrotic cardiac tissue development comprising the following essential processes: (i) adhesion to substrates with varying elasticity, (ii) dynamics of contractile function, and (iii) electromechanical connectivity. By combining electric cell-substrate impedance sensing (ECIS) with conventional optical microscopy, we could measure the impact of fibroblast-cardiomyocyte ratio on the aforementioned parameters in a non-invasive fashion. Adhesion to electrodes was quantified via spreading rates derived from impedance changes, period analysis allowed us to measure contraction dynamics and modulations of the barrier resistance served as a measure of connectivity. In summary, we claim that: (i) a preferred window for substrate elasticity around 7 kPa for low fibroblast content exists, which is shifted to stiffer substrates with increasing fibroblast fractions. (ii) Beat frequency decreases nonlinearly with increasing fraction of fibroblasts, while (iii) the intercellular resistance increases with a maximal functional connectivity at 75% fibroblasts. For the first time, cardiac cell-cell junction density-dependent connectivity in co-cultures of cardiomyocytes and fibroblasts was quantified using ECIS.

Indexed as

Cell CommunicationElectric ImpedanceAnimalsAnimals, NewbornCells, CulturedCoculture TechniquesFibroblastsImage Processing, Computer-AssistedImmunoenzyme TechniquesMicroscopy, Atomic ForceMyocytes, CardiacRatsRats, Wistarcardiomyocytescontractile functionelectric cell-substrate impedance sensingfibroblastsfibrosisimpedance spectroscopy

Identifiers

PMID26085516
PMCPMC4632504

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.