Evidence map›Paper›PMID 33798964›Full record

ArticleBiomaterials2021

Tunable electroconductive decellularized extracellular matrix hydrogels for engineering human cardiac microphysiological systems.

Jonathan H Tsui, Andrea Leonard, Nathan D Camp, Joseph T Long, Zeid Y Nawas, Rakchanok Chavanachat, Alec S T Smith, Jong Seob Choi, Zhipeng Dong, Eun Hyun Ahn and 4 more

Open access · greenAbstract read
In one paragraph

Article in Biomaterials, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed, 1 pooled it
17.6field-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

61 citing papers in PubMed, 1 synthesis or guideline pooled it, 111 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Conductive Hydrogels for Exogenous Sensing and Cell Fate Control.Advanced materials (Deerfield Beach, Fla.) · 2026
    Article
  4. Article
  5. Article
  6. Review
  7. 3D Bioprinting Functional Engineered Heart Tissues.International journal of molecular sciences · 2025
    Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Novel Electroactive Therapeutic Platforms for Cardiac Arrhythmia Management.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
  15. Article
  16. Review
  17. Review
  18. Heterogeneous and Composite Bioinks for 3D-Bioprinting of Complex Tissue.Biomedical materials & devices (New York, N.Y.) · 2025
    Review
  19. Review
  20. Review

1 more citing papers are in PubMed but not listed here.

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

14 authors at 2 institutions in 1 country.

Jonathan H TsuiDepartment of Biomedical Engineering, Johns Hopkins University, Baltimore, MD, 21205, USA.
Andrea LeonardDepartment of Mechanical Engineering, University of Washington, Seattle, WA, 98105, USA.
Nathan D CampDepartment of Genome Sciences, University of Washington, Seattle, WA, 98105, USA.
Joseph T LongDepartment of Bioengineering, University of Washington, Seattle, WA, 98105, USA.
Zeid Y NawasDepartment of Bioengineering, University of Washington, Seattle, WA, 98105, USA.
Rakchanok ChavanachatDepartment of Bioengineering, University of Washington, Seattle, WA, 98105, USA.
Alec S T SmithDepartment of Physiology and Biophysics, University of Washington, Seattle, WA, 98105, USA; Institute for Stem Cell & Regenerative Medicine, University of Washington, Seattle, WA, 98109, USA.
Jong Seob ChoiDepartment of Biomedical Engineering, Johns Hopkins University, Baltimore, MD, 21205, USA.
Zhipeng DongDepartment of Biomedical Engineering, Johns Hopkins University, Baltimore, MD, 21205, USA.
Eun Hyun AhnDepartment of Biomedical Engineering, Johns Hopkins University, Baltimore, MD, 21205, USA.
Alejandro Wolf-YadlinDepartment of Genome Sciences, University of Washington, Seattle, WA, 98105, USA.
Charles E MurryDepartment of Bioengineering, University of Washington, Seattle, WA, 98105, USA; Department of Pathology, University of Washington, Seattle, WA, 98109, USA; Center for Cardiovascular Biology, University of Washington, Seattle, WA, 98109, USA; Institute for Stem Cell & Regenerative Medicine, University of Washington, Seattle, WA, 98109, USA.
Nathan J SniadeckiDepartment of Mechanical Engineering, University of Washington, Seattle, WA, 98105, USA; Department of Bioengineering, University of Washington, Seattle, WA, 98105, USA; Center for Cardiovascular Biology, University of Washington, Seattle, WA, 98109, USA; Institute for Stem Cell & Regenerative Medicine, University of Washington, Seattle, WA, 98109, USA.
Deok-Ho KimDepartment of Biomedical Engineering, Johns Hopkins University, Baltimore, MD, 21205, USA; Division of Cardiology, Department of Medicine, Johns Hopkins University, Baltimore, MD, 21205, USA. Electronic address: dhkim@jhu.edu.
University of Washington · USJohns Hopkins University · US

Funding

NRSA Training CoreTL1TR002318 · NCATS · UNIVERSITY OF WASHINGTON · PI Megan Moore · 2017 to 2026
$8.4M
DISEASE MODELING AND PHENOTYPIC DRUG SCREENING FOR DYSTROPHIC CARDIOMYOPATHYR01HL146436 · NHLBI · UNIVERSITY OF WASHINGTON · PI KIM, DEOK-HO · 2019 to 2022
$2.2M
Mechanotransduction by Melusin in Cardiac HypertrophyR01HL149734 · NHLBI · UNIVERSITY OF WASHINGTON · PI SNIADECKI, NATHAN JOHN · 2020 to 2023
$2.1M
A Human iPSC-based 3D Microphysiological System for Modeling Cardiac Dysfunction in MicrogravityUH3TR003519 · NCATS · JOHNS HOPKINS UNIVERSITY · PI KIM, DEOK-HO · 2020 to 2022
$2.0M
A NANOPATTERNED MEA-BASED FUNCTIONAL PHENOTYPING ASSAY FOR DRUG-INDUCED CARDIOTOXICITY SCREENINGR01HL135143 · NHLBI · UNIVERSITY OF WASHINGTON · PI KIM, DEOK-HO · 2017 to 2021
$1.9M
A HUMAN IPSC-BASED 3D MICROPHYSIOLOGICAL SYSTEM FOR MODELING CARDIAC DYSFUNCTION IN MICROGRAVITYUG3EB028094 · NIBIB · UNIVERSITY OF WASHINGTON · PI KIM, DEOK-HO · 2018 to 2019
$1.5M
Injectable myocardial matrix-grapheme composite hydrogels for functional cardiac tissue engineeringR21EB020132 · NIBIB · UNIVERSITY OF WASHINGTON · PI KIM, DEOK-HO · 2016 to 2017
$435k
Integrins, mechanotransduction, and the maturation of cardiomyocytes derived from induced pluripotent stem cellsF32HL126332 · NHLBI · UNIVERSITY OF WASHINGTON · PI LEONARD, ANDREA B · 2015 to 2017
$164k
NCATS NIH HHS TL1 TR002318NCATS NIH HHS UH3 TR003519NHLBI NIH HHS F32 HL126332NHLBI NIH HHS R01 HL135143NHLBI NIH HHS R01 HL146436NHLBI NIH HHS R01 HL149734NIBIB NIH HHS R21 EB020132NIBIB NIH HHS UG3 EB028094
6 · The paper itself

Abstract

Cardiomyocytes differentiated from human induced pluripotent stem cells (hiPSCs) offer tremendous potential when used to engineer human tissues for drug screening and disease modeling; however, phenotypic immaturity reduces assay reliability when translating in vitro results to clinical studies. To address this, we have developed hybrid hydrogels comprised of decellularized porcine myocardial extracellular matrix (dECM) and reduced graphene oxide (rGO) to provide a more instructive microenvironment for proper cell and tissue development. A tissue-specific protein profile was preserved post-decellularization, and through the modulation of rGO content and degree of reduction, the mechanical and electrical properties of the hydrogels could be tuned. Engineered heart tissues (EHTs) generated using dECM-rGO hydrogel scaffolds and hiPSC-derived cardiomyocytes exhibited significantly increased twitch forces and had increased expression of genes that regulate contractile function. Improvements in various aspects of electrophysiological function, such as calcium-handling, action potential duration, and conduction velocity, were also induced by the hybrid biomaterial. dECM-rGO hydrogels could also be used as a bioink to print cardiac tissues in a high-throughput manner, and these tissues were utilized to assess the proarrhythmic potential of cisapride. Action potential prolongation and beat interval irregularities was observed in dECM-rGO tissues at clinical doses of cisapride, indicating that the enhanced electrophysiological function of these tissues corresponded well with a capability to produce physiologically relevant drug responses.

Indexed as

HydrogelsInduced Pluripotent Stem CellsAnimalsExtracellular MatrixHumansReproducibility of ResultsSwineTissue EngineeringTissue ScaffoldsHydrogelsBioprintingCardiac tissue engineeringDecellularized extracellular matrixGraphene oxideHybrid materials

Identifiers

PMID33798964
PMCPMC8074529
OpenAlexW3138947005

What OpenQuestion holds

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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.