Evidence map›Paper›PMID 40520527›Full record

ArticleJournal of tissue engineering and regenerative medicine2025

Short-Term Electrical Stimulation Impacts Cardiac Cell Structure and Function.

Kristen Allen, Natalie Pachter, Abigail Bandl, Haleema Qamar, Alex Ropars, Tracy A Hookway

Abstract read
In one paragraph

Article in Journal of tissue engineering and regenerative medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

6 authors.

Kristen AllenDepartment of Biomedical Engineering, Binghamton University, The State University of New York, Binghamton, New York 13902, USA.ORCID https://orcid.org/0009-0006-1277-5585
Natalie PachterDepartment of Biomedical Engineering, Binghamton University, The State University of New York, Binghamton, New York 13902, USA.ORCID https://orcid.org/0000-0003-2788-5630
Abigail BandlDepartment of Biomedical Engineering, Binghamton University, The State University of New York, Binghamton, New York 13902, USA.
Haleema QamarDepartment of Biomedical Engineering, Binghamton University, The State University of New York, Binghamton, New York 13902, USA.ORCID https://orcid.org/0000-0003-1599-4020
Alex RoparsDepartment of Biomedical Engineering, Binghamton University, The State University of New York, Binghamton, New York 13902, USA.ORCID https://orcid.org/0009-0008-9237-9068
Tracy A HookwayDepartment of Biomedical Engineering, Binghamton University, The State University of New York, Binghamton, New York 13902, USA.ORCID https://orcid.org/0000-0003-2781-0911

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Induced pluripotent stem cell-derived cardiomyocytes (iPSC-CMs) are used to model cardiac development and disease. This requires a robust population of mature CMs and external stimuli to mimic the complex environment of the heart. In effort toward this maturation, previous groups have applied electrical stimulation (ES) to CMs with varying results depending on the stimulation duration, frequency, and pattern. As such, there is an uncertainty surrounding the timeline on which stimulated iPSC-CMs begin to show early signs of maturation in comparison with their nonstimulated counterparts. Here, we introduce a low-cost custom bioreactor capable of delivering tunable ES to standard 2D cell monolayers. We show that, after exposure to short-term ES, stimulated CMs express early signs of maturation compared to nonstimulated controls. Changes to contractility and protein expression indicate cellular rearrangement within cell monolayers and induction of partial maturation in response to ES. While early signs of maturation are present after 3-4 days of ES, additional cellular structures must develop to reach complete maturation. We also show that this bioreactor can electrically stimulate cardiac fibroblasts (cFBs) and may induce alignment of cFB. We have shown that our custom ES bioreactor can be easily integrated into standard in vitro cell culture platforms to induce measurable changes in both CMs and cFB, exhibiting its potential for promoting crucial CM maturation and cell alignment for cardiac tissue engineering applications.

Indexed as

Electric StimulationInduced Pluripotent Stem CellsMyocytes, CardiacAnimalsBioreactorsCell DifferentiationFibroblastsHumanscardiomyocytescontractilityelectrical stimulationinduced pluripotent stem cellin vitro modelingmaturation

Identifiers

PMID40520527
PMCPMC12165760

What OpenQuestion holds

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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.