Evidence map›Paper›PMID 38519491›Full record

ArticleNature communications2024

Versatile human cardiac tissues engineered with perfusable heart extracellular microenvironment for biomedical applications.

Sungjin Min, Suran Kim, Woo-Sup Sim, Yi Sun Choi, Hyebin Joo, Jae-Hyun Park, Su-Jin Lee, Hyeok Kim, Mi Jeong Lee, Inhea Jeong and 11 more

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing 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

62 citing papers in PubMed.

  1. Article
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  3. Human cardiovascular organoids: Biomedical applications and ethical challenges.American heart journal plus : cardiology research and practice · 2026
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2 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

21 authors.

Sungjin Min *Department of Biotechnology, Yonsei University, Seoul, 03722, Republic of Korea.ORCID http://orcid.org/0000-0002-5041-8638
Suran Kim *Department of Biotechnology, Yonsei University, Seoul, 03722, Republic of Korea.
Woo-Sup Sim *Department of Biomedicine & Health Sciences, College of Medicine, The Catholic University of Korea, Seoul, 06591, Republic of Korea.ORCID http://orcid.org/0000-0001-7425-8192
Yi Sun ChoiDepartment of Biotechnology, Yonsei University, Seoul, 03722, Republic of Korea.ORCID http://orcid.org/0000-0002-4691-8875
Hyebin JooDepartment of Biotechnology, Yonsei University, Seoul, 03722, Republic of Korea.
Jae-Hyun ParkDepartment of Biomedicine & Health Sciences, College of Medicine, The Catholic University of Korea, Seoul, 06591, Republic of Korea.
Su-Jin LeeDepartment of Predictive Toxicology, Korea Institute of Toxicology, Daejeon, 34114, Republic of Korea.
Hyeok KimDepartment of Biomedicine & Health Sciences, College of Medicine, The Catholic University of Korea, Seoul, 06591, Republic of Korea.ORCID http://orcid.org/0000-0001-9184-5882
Mi Jeong LeeDepartment of Biotechnology, Yonsei University, Seoul, 03722, Republic of Korea.ORCID http://orcid.org/0000-0003-4807-9558
Inhea JeongDepartment of Materials Science and Engineering, Yonsei University, Seoul, 03722, Republic of Korea.ORCID http://orcid.org/0000-0003-2226-4755
Baofang CuiDepartment of Biotechnology, Yonsei University, Seoul, 03722, Republic of Korea.
Sung-Hyun JoDepartment of Chemical Engineering, Soongsil University, Seoul, 06978, Republic of Korea.ORCID http://orcid.org/0000-0002-2854-1568
Jin-Ju KimDepartment of Biomedicine & Health Sciences, College of Medicine, The Catholic University of Korea, Seoul, 06591, Republic of Korea.
Seok Beom HongDepartment of Thoracic and Cardiovascular Surgery, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, 06591, Republic of Korea.
Yeon-Jik ChoiDivision of Cardiology, Department of Internal Medicine, Eunpyeong St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, 03312, Republic of Korea.
Kiwon BanDepartment of Biomedical Sciences, City University of Hong Kong, Kowloon, 999077, Hong Kong.
Yun-Gon KimDepartment of Chemical Engineering, Soongsil University, Seoul, 06978, Republic of Korea.
Jang-Ung ParkDepartment of Materials Science and Engineering, Yonsei University, Seoul, 03722, Republic of Korea.
Hyang-Ae LeeDepartment of Predictive Toxicology, Korea Institute of Toxicology, Daejeon, 34114, Republic of Korea.ORCID http://orcid.org/0000-0002-0036-4555
Hun-Jun ParkDepartment of Biomedicine & Health Sciences, College of Medicine, The Catholic University of Korea, Seoul, 06591, Republic of Korea. cardioman@catholic.ac.kr.ORCID http://orcid.org/0000-0001-8009-9546
Seung-Woo ChoDepartment of Biotechnology, Yonsei University, Seoul, 03722, Republic of Korea. seungwoocho@yonsei.ac.kr.ORCID http://orcid.org/0000-0001-8058-332X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Engineered human cardiac tissues have been utilized for various biomedical applications, including drug testing, disease modeling, and regenerative medicine. However, the applications of cardiac tissues derived from human pluripotent stem cells are often limited due to their immaturity and lack of functionality. Therefore, in this study, we establish a perfusable culture system based on in vivo-like heart microenvironments to improve human cardiac tissue fabrication. The integrated culture platform of a microfluidic chip and a three-dimensional heart extracellular matrix enhances human cardiac tissue development and their structural and functional maturation. These tissues are comprised of cardiovascular lineage cells, including cardiomyocytes and cardiac fibroblasts derived from human induced pluripotent stem cells, as well as vascular endothelial cells. The resultant macroscale human cardiac tissues exhibit improved efficacy in drug testing (small molecules with various levels of arrhythmia risk), disease modeling (Long QT Syndrome and cardiac fibrosis), and regenerative therapy (myocardial infarction treatment). Therefore, our culture system can serve as a highly effective tissue-engineering platform to provide human cardiac tissues for versatile biomedical applications.

Indexed as

Endothelial CellsInduced Pluripotent Stem CellsCell DifferentiationHumansMyocytes, CardiacTissue Engineering

Identifiers

PMID38519491
PMCPMC10960018

What OpenQuestion holds

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Registered trials

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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.