Evidence map›Paper›PMID 40582540›Full record

ArticleActa biomaterialia2026

Advanced tissue-engineered pulsatile conduit using human induced pluripotent stem cell-derived cardiomyocytes.

Hangqi Luo, Christopher W Anderson, Xin Li, Yinsheng Lu, Marie Hoareau, Qinzhe Xing, Saba Fooladi, Yufeng Liu, Zhen Xu, Jinkyu Park and 8 more

Abstract read
In one paragraph

Article in Acta biomaterialia, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

18 authors.

Hangqi LuoYale Cardiovascular Research Center, Section of Cardiovascular Medicine, Department of Internal Medicine Yale School of Medicine, New Haven, CT 06511, United States; Yale Stem Cell Center, New Haven, CT 06520, United States; Vascular Biology and Therapeutics Program, Yale University School of Medicine, New Haven, CT 06520, United States.
Christopher W AndersonYale Cardiovascular Research Center, Section of Cardiovascular Medicine, Department of Internal Medicine Yale School of Medicine, New Haven, CT 06511, United States; Yale Stem Cell Center, New Haven, CT 06520, United States; Department of Bioengineering, University of California San Diego, 9500 Gilman Dr, La Jolla, CA 92093, United States.
Xin LiYale Cardiovascular Research Center, Section of Cardiovascular Medicine, Department of Internal Medicine Yale School of Medicine, New Haven, CT 06511, United States; Yale Stem Cell Center, New Haven, CT 06520, United States; Vascular Biology and Therapeutics Program, Yale University School of Medicine, New Haven, CT 06520, United States.
Yinsheng LuYale Cardiovascular Research Center, Section of Cardiovascular Medicine, Department of Internal Medicine Yale School of Medicine, New Haven, CT 06511, United States; Yale Stem Cell Center, New Haven, CT 06520, United States; Vascular Biology and Therapeutics Program, Yale University School of Medicine, New Haven, CT 06520, United States; Department of Mechanical Engineering and Materials Science, Yale University, New Haven, CT 06510, United States.
Marie HoareauYale Cardiovascular Research Center, Section of Cardiovascular Medicine, Department of Internal Medicine Yale School of Medicine, New Haven, CT 06511, United States; Yale Stem Cell Center, New Haven, CT 06520, United States; Vascular Biology and Therapeutics Program, Yale University School of Medicine, New Haven, CT 06520, United States.
Qinzhe XingYale Cardiovascular Research Center, Section of Cardiovascular Medicine, Department of Internal Medicine Yale School of Medicine, New Haven, CT 06511, United States; Yale Stem Cell Center, New Haven, CT 06520, United States; Vascular Biology and Therapeutics Program, Yale University School of Medicine, New Haven, CT 06520, United States; Department of Biomedical Engineering, Yale University, New Haven, CT 06510, United States.
Saba FooladiYale Cardiovascular Research Center, Section of Cardiovascular Medicine, Department of Internal Medicine Yale School of Medicine, New Haven, CT 06511, United States; Yale Stem Cell Center, New Haven, CT 06520, United States; Vascular Biology and Therapeutics Program, Yale University School of Medicine, New Haven, CT 06520, United States; Department of Biomedical Engineering, Yale University, New Haven, CT 06510, United States.
Yufeng LiuYale Cardiovascular Research Center, Section of Cardiovascular Medicine, Department of Internal Medicine Yale School of Medicine, New Haven, CT 06511, United States; Yale Stem Cell Center, New Haven, CT 06520, United States; Vascular Biology and Therapeutics Program, Yale University School of Medicine, New Haven, CT 06520, United States; Department of Pathology, Yale University, New Haven, CT 06520, United States.
Zhen XuYale Cardiovascular Research Center, Section of Cardiovascular Medicine, Department of Internal Medicine Yale School of Medicine, New Haven, CT 06511, United States; Yale Stem Cell Center, New Haven, CT 06520, United States; Vascular Biology and Therapeutics Program, Yale University School of Medicine, New Haven, CT 06520, United States.
Jinkyu ParkYale Cardiovascular Research Center, Section of Cardiovascular Medicine, Department of Internal Medicine Yale School of Medicine, New Haven, CT 06511, United States; Yale Stem Cell Center, New Haven, CT 06520, United States; Vascular Biology and Therapeutics Program, Yale University School of Medicine, New Haven, CT 06520, United States; Department of Physiology, College of Medicine, Hallym University, Hallymdaehak-gil, Chuncheon-si, Gangwon-Do 24252, South Korea.
Meghan E FallonYale Cardiovascular Research Center, Section of Cardiovascular Medicine, Department of Internal Medicine Yale School of Medicine, New Haven, CT 06511, United States; Yale Stem Cell Center, New Haven, CT 06520, United States; Vascular Biology and Therapeutics Program, Yale University School of Medicine, New Haven, CT 06520, United States.
Jordan ThomasDepartment of Biomedical Engineering, Yale University, New Haven, CT 06510, United States.
Peter J GruberDepartment of Pathology, Yale University, New Haven, CT 06520, United States; Department of Surgery, Yale University, New Haven, CT 06520, United States.
Robert W ElderYale Cardiovascular Research Center, Section of Cardiovascular Medicine, Department of Internal Medicine Yale School of Medicine, New Haven, CT 06511, United States; Department of Pediatrics, Yale School of Medicine, New Haven, CT 06520, United States.
Michael MakYale Cardiovascular Research Center, Section of Cardiovascular Medicine, Department of Internal Medicine Yale School of Medicine, New Haven, CT 06511, United States; Department of Biomedical Engineering, Yale University, New Haven, CT 06510, United States; Department of Pharmacological Sciences, Renaissance School of Medicine, Stony Brook University, Stony Brook, NY 11794, United States.
Muhammad RiazYale Cardiovascular Research Center, Section of Cardiovascular Medicine, Department of Internal Medicine Yale School of Medicine, New Haven, CT 06511, United States; Yale Stem Cell Center, New Haven, CT 06520, United States; Vascular Biology and Therapeutics Program, Yale University School of Medicine, New Haven, CT 06520, United States.
Stuart G CampbellDepartment of Biomedical Engineering, Yale University, New Haven, CT 06510, United States.
Yibing QyangYale Cardiovascular Research Center, Section of Cardiovascular Medicine, Department of Internal Medicine Yale School of Medicine, New Haven, CT 06511, United States; Yale Stem Cell Center, New Haven, CT 06520, United States; Vascular Biology and Therapeutics Program, Yale University School of Medicine, New Haven, CT 06520, United States; Department of Biomedical Engineering, Yale University, New Haven, CT 06510, United States; Department of Pathology, Yale University, New Haven, CT 06520, United States. Electronic address: yibing.qyang@yale.edu.

Funding

Readily Available Stem Cell-Based Vascular Grafts for Emergent Surgical CareR01HL150352 · NHLBI · YALE UNIVERSITY · PI QYANG, YIBING · 2020 to 2023
$2.8M
Human tissue-engineered blood vessels using induced pluripotent stem cellsR01HL116705 · NHLBI · YALE UNIVERSITY · PI QYANG, YIBING · 2013 to 2017
$2.0M
Readily Available Biological Conduits to Treat Single Ventricle DefectsR01HL171984 · NHLBI · YALE UNIVERSITY · PI Yibing Qyang · 2024 to 2026
$1.7M
Development of HLA engineered universal vascular grafts from human iPSCsR01HL155411 · NHLBI · YALE UNIVERSITY · PI QYANG, YIBING · 2021 to 2024
$1.7M
PRODUCING PIG INDUCED PLURIPOTENT STEM CELLS FOR CARDIOVASCULAR TISSUE ENGINEERINGF31HL149289 · NHLBI · YALE UNIVERSITY · PI BATTY, LUKE DANIEL · 2019 to 2021
$126k
NHLBI NIH HHS F31 HL149289NHLBI NIH HHS R01 HL116705NHLBI NIH HHS R01 HL150352NHLBI NIH HHS R01 HL155411NHLBI NIH HHS R01 HL171984
6 · The paper itself

Abstract

Single ventricle congenital heart defects (SVCHDs) are life-threatening defects that can lead to severe circulation issues and increased stress on the heart. Without prompt treatment, these defects can prove fatal in infancy. Fontan surgery is a conventional treatment for SVCHDs, which reroutes oxygen-poor blood directly to the lungs, bypassing the non-functioning ventricle. This procedure, however, can lead to circulation inefficiencies due to the absence of a natural, functional ventricle to pump blood to the pulmonary circulation. To address this issue, our team previously developed a tissue-engineered pulsatile conduit (TEPC) by wrapping engineered heart tissues (EHTs) derived from human induced pluripotent stem cell-derived cardiomyocytes (hiPSCCMs) around decellularized human umbilical artery (dHUA). This conduit has demonstrated the ability to produce a luminal pressure of 0.68 mmHg from spontaneous beating, which under 2 Hz electrical stimulation, increases to 0.83 mmHg. This offers a promising modular TEPC design that has the potential to provide active pumping function to the pulmonary circulation. We have since significantly optimized our approach by providing the conduit with electrical pacing training and an additional layer of EHT. These two enhancements have achieved markedly greater contractile productivity, where the spontaneous pressure generation reached 0.96 mmHg and the stimulated luminal pressure generation attained 1.87 mmHg with 2 Hz pacing. Our studies thus underscore the effectiveness of these TEPC design modifications, marking significant progress in the ongoing effort to improve treatments for patients with SVCHDs. STATEMENT OF SIGNIFICANCE: Single ventricle congenital heart defects (SVCHDs) are a life-threatening disorder, leading to severe circulation issues and heart failure. The Fontan procedure reroutes blood to the lung but lacks active pumping required for efficient circulation, often causing long-term complications. To address this challenge, we developed a tissue-engineered pulsatile conduit (TEPC) using human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) and decellularized human umbilical artery (dHUA) scaffolds. Our optimized design, with electrical pacing and enhanced engineered heart tissue (EHT) approaches, significantly increased luminal pressure development (up to 1.87 mmHg at 2 Hz frequency), offering a promising solution to improve outcomes for SVCHD patients.

Indexed as

CardiomyocytesEngineered heart tissueHuman induced pluripotent stem cellsTissue-engineered pulsatile conduit

Identifiers

PMID40582540
PMCPMC12338880

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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.