Evidence map›Paper›PMID 38241367›Full record

ArticleScience advances2024

Engineered cocultures of iPSC-derived atrial cardiomyocytes and atrial fibroblasts for modeling atrial fibrillation.

Grace E Brown, Yong Duk Han, Ashlin R Michell, Olivia T Ly, Carlos G Vanoye, Emanuele Spanghero, Alfred L George, Dawood Darbar, Salman R Khetani

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
8.9field-weighted citation impact, top 1% 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

27 citing papers in PubMed, 33 citations in OpenAlex.

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  17. Animal and cellular models of atrial fibrillation: a review.Frontiers in cardiovascular medicine · 2025
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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 at 2 institutions in 1 country.

Grace E BrownDepartment of Biomedical Engineering, University of Illinois at Chicago, Chicago, IL, USA.ORCID 0000-0002-1071-0108
Yong Duk HanDepartment of Biomedical Engineering, University of Illinois at Chicago, Chicago, IL, USA.
Ashlin R MichellDepartment of Biomedical Engineering, University of Illinois at Chicago, Chicago, IL, USA.ORCID 0000-0002-7563-4345
Olivia T LyDepartment of Biomedical Engineering, University of Illinois at Chicago, Chicago, IL, USA.
Carlos G VanoyeDepartment of Pharmacology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.ORCID 0000-0002-4935-1122
Emanuele SpangheroDepartment of Biomedical Engineering, University of Illinois at Chicago, Chicago, IL, USA.ORCID 0000-0003-3891-1961
Alfred L GeorgeDepartment of Pharmacology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.ORCID 0000-0002-3993-966X
Dawood DarbarDepartment of Biomedical Engineering, University of Illinois at Chicago, Chicago, IL, USA.ORCID 0000-0002-4103-5977
Salman R KhetaniDepartment of Biomedical Engineering, University of Illinois at Chicago, Chicago, IL, USA.ORCID 0000-0002-5407-6743
University of Illinois Chicago · USNorthwestern University · US

Funding

TRAINING PROGRAM IN LUNG BIOLOGY AND PATHOBIOLOGYT32HL007829 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI DOLLY MEHTA · 1995 to 2026
$15.6M
Genotype-guided therapy for atrial fibrillationR01HL148444 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI DARBAR, DAWOOD · 2020 to 2024
$3.5M
Human iPSC-derived atrial cardiomyocytes to model atrial fibrillation in a dishR01HL150586 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI DARBAR, DAWOOD, KHETANI, SALMAN R · 2020 to 2023
$2.6M
Training Program in Personalized Cardiovascular Medicine (TPIPCVM)T32HL139439 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI DARBAR, DAWOOD · 2018 to 2022
$2.1M
Obesity-Mediated Atrial Fibrillation: Underlying Mechanisms and Responsiveness to Antiarrhythmic TherapyI01BX004268 · VA · JESSE BROWN VA MEDICAL CENTER · PI DARBAR, DAWOOD · 2019 to 2023
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BLRD VA I01 BX004268NHLBI NIH HHS R01 HL148444NHLBI NIH HHS R01 HL150586NHLBI NIH HHS T32 HL007829NHLBI NIH HHS T32 HL139439
6 · The paper itself

Abstract

Atrial fibrillation (AF) is the most common sustained cardiac arrhythmia treatable with antiarrhythmic drugs; however, patient responses remain highly variable. Human induced pluripotent stem cell-derived atrial cardiomyocytes (iPSC-aCMs) are useful for discovering precision therapeutics, but current platforms yield phenotypically immature cells and are not easily scalable for high-throughput screening. Here, primary adult atrial, but not ventricular, fibroblasts induced greater functional iPSC-aCM maturation, partly through connexin-40 and ephrin-B1 signaling. We developed a protein patterning process within multiwell plates to engineer patterned iPSC-aCM and atrial fibroblast coculture (PC) that significantly enhanced iPSC-aCM structural, electrical, contractile, and metabolic maturation for 6+ weeks compared to conventional mono-/coculture. PC displayed greater sensitivity for detecting drug efficacy than monoculture and enabled the modeling and pharmacological or gene editing treatment of an AF-like electrophysiological phenotype due to a mutated sodium channel. Overall, PC is useful for elucidating cell signaling in the atria, drug screening, and modeling AF.

Indexed as

Atrial FibrillationInduced Pluripotent Stem CellsAdultCoculture TechniquesFibroblastsHumansMyocytes, Cardiac

Identifiers

PMID38241367
PMCPMC10798559
OpenAlexW4391019517

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.