Evidence map›Paper›PMID 42394910›Full record

ArticleBioengineering & translational medicine2026

Open-source bioreactor delivers electrical and perfusion stimulation supporting 3D cardiac engineered tissue maturation.

Gregory Reid, Stefano Gabetti, Antonio Sileo, Deborah Fusco, Giuseppe Isu, Diana Massai, Giulia Milan, Anna Marsano

Abstract read
In one paragraph

Article in Bioengineering & translational medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Gregory ReidDepartment of Biomedicine University of Basel and University Hospital of Basel Basel Switzerland.
Stefano GabettiDepartment of Mechanical and Aerospace Engineering and PolitoBIOMed Lab Politecnico di Torino Turin Italy.
Antonio SileoDepartment of Biomedicine University of Basel and University Hospital of Basel Basel Switzerland.
Deborah FuscoDepartment of Biomedicine University of Basel and University Hospital of Basel Basel Switzerland.
Giuseppe IsuDepartment of Biomedicine University of Basel and University Hospital of Basel Basel Switzerland.
Diana MassaiDepartment of Mechanical and Aerospace Engineering and PolitoBIOMed Lab Politecnico di Torino Turin Italy.
Giulia MilanDepartment of Biomedicine University of Basel and University Hospital of Basel Basel Switzerland.
Anna MarsanoDepartment of Biomedicine University of Basel and University Hospital of Basel Basel Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cardiac tissue engineering requires control over physical stimuli, such as mechanical and electrical, to promote the maturation and functionality of cardiomyocytes. While perfusion bioreactors and electrical stimulation systems have been employed before, their synergistic impact, specifically when using direct perfusion in soft hydrogel environments, remains underexplored. We developed a cost-effective, modified perfusion bioreactor that is commercially available, to integrate electrical stimulation to support the culture of fibrin-based cardiac constructs. The system delivers continuous unidirectional flow (0.3 mL/min) and controlled electrical pulses (3 V/cm, 1 Hz), with validated flow and field uniformity via computational fluid dynamics and finite element analysis simulations. Neonatal rat cardiac cell-based constructs were cultured either under static or perfusion conditions in presence or not of electrical stimulation. Cellular outcomes were evaluated by immunofluorescence, gene expression, and live-cell functional analyses. Perfusion significantly improved cell retention and cardiomyocyte yield, while electrical stimulation promoted cardiomyocyte elongation, sarcomere organization, and maturation. The combination of perfusion and electrical stimulation led to the highest proportion of mature cardiomyocytes (51.4%), significantly outperforming perfusion alone (12.3%), static combined with electrical stimulation (22.2%), and static alone (7.5%). A reduced fibroblast activation was observed, along with enhanced tissue remodeling, as shown by increased extracellular matrix density and upregulation of remodeling genes. Functionally, constructs under perfusion with electrical stimulation exhibited the lowest excitation thresholds, highest maximum capture rates, and the greatest contraction displacement (2.2 ± 0.49 V, 4.2 ± 0.71 Hz, 13.35 ± 3.6 μm respectively), confirming superior functional performance. Our integrated bioreactor system enables efficient culture of soft 3D cardiac tissues and demonstrates that combining perfusion with electrical stimulation synergistically enhances cardiomyocyte maturation, construct remodeling, and functional performance. Beyond being a promising tool, this platform represents a powerful and scalable solution for cardiac tissue engineering, with potential for applications in disease modeling, drug screening, and regenerative medicine.

Indexed as

bioreactorcardiomyocyteelectrical stimulationin vitro cardiac modelsperfusiontissue engineering

Identifiers

PMID42394910
PMCPMC13327607

What Socratic holds

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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 Socratic graph.