Evidence map›Paper›PMID 37293290›Full record

ArticleFrontiers in cardiovascular medicine2023

3D-bioprinting of patient-derived cardiac tissue models for studying congenital heart disease.

Jayne T Wolfe, Wei He, Min-Su Kim, Huan-Ling Liang, Akankshya Shradhanjali, Hilda Jurkiewicz, Bonnie P Freudinger, Andrew S Greene, John F LaDisa, Lobat Tayebi and 3 more

Abstract read
In one paragraph

Article in Frontiers in cardiovascular medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

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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

13 authors.

Jayne T WolfeDepartment of Biomedical Engineering, Medical College of Wisconsin & Marquette University, Milwaukee, WI, United States.
Wei HeDepartment of Biomedical Engineering, Medical College of Wisconsin & Marquette University, Milwaukee, WI, United States.
Min-Su KimDepartment of Surgery, Medical College of Wisconsin, Milwaukee, WI, United States.
Huan-Ling LiangDepartment of Surgery, Medical College of Wisconsin, Milwaukee, WI, United States.
Akankshya ShradhanjaliDepartment of Biomedical Engineering, Medical College of Wisconsin & Marquette University, Milwaukee, WI, United States.
Hilda JurkiewiczDepartment of Biomedical Engineering, Medical College of Wisconsin & Marquette University, Milwaukee, WI, United States.
Bonnie P FreudingerEngineering Core, Medical College of Wisconsin, Milwaukee, WI, United States.
Andrew S GreeneThe Jackson Laboratory, Bar Harbor, ME, United States.
John F LaDisaDepartment of Biomedical Engineering, Medical College of Wisconsin & Marquette University, Milwaukee, WI, United States.
Lobat TayebiSchool of Dentistry, Marquette University, Milwaukee, WI, United States.
Michael E MitchellDepartment of Surgery, Medical College of Wisconsin, Milwaukee, WI, United States.
Aoy Tomita-MitchellDepartment of Biomedical Engineering, Medical College of Wisconsin & Marquette University, Milwaukee, WI, United States.
Brandon J TefftDepartment of Biomedical Engineering, Medical College of Wisconsin & Marquette University, Milwaukee, WI, United States.

Funding

Clinical and Translational Science AwardUL1TR001436 · NCATS · MEDICAL COLLEGE OF WISCONSIN · PI FREED, JULIE K · 2015 to 2025
$47.5M
NCATS NIH HHS UL1 TR001436
6 · The paper itself

Abstract

Introduction: Congenital heart disease is the leading cause of death related to birth defects and affects 1 out of every 100 live births. Induced pluripotent stem cell technology has allowed for patient-derived cardiomyocytes to be studied in vitro. An approach to bioengineer these cells into a physiologically accurate cardiac tissue model is needed in order to study the disease and evaluate potential treatment strategies. Methods: To accomplish this, we have developed a protocol to 3D-bioprint cardiac tissue constructs comprised of patient-derived cardiomyocytes within a hydrogel bioink based on laminin-521. Results: Cardiomyocytes remained viable and demonstrated appropriate phenotype and function including spontaneous contraction. Contraction remained consistent during 30 days of culture based on displacement measurements. Furthermore, tissue constructs demonstrated progressive maturation based on sarcomere structure and gene expression analysis. Gene expression analysis also revealed enhanced maturation in 3D constructs compared to 2D cell culture. Discussion: This combination of patient-derived cardiomyocytes and 3D-bioprinting represents a promising platform for studying congenital heart disease and evaluating individualized treatment strategies.

Indexed as

3D-bioprintingcardiomyocytecongenital heart diseasehydrogelhypoplastic left heart syndromeinduced pluripotent stem cell

Identifiers

PMID37293290
PMCPMC10247285

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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.