Evidence map›Paper›PMID 24819474›Full record

ReviewAnnual review of biomedical engineering2014

Heart regeneration with engineered myocardial tissue.

Kareen L K Coulombe, Vivek K Bajpai, Stelios T Andreadis, Charles E Murry

Abstract readReview
In one paragraph

Review in Annual review of biomedical engineering, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
11.7field-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

48 citing papers in PubMed, 81 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
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  7. Article
  8. Cardiac preservation usingFrontiers in cardiovascular medicine · 2025
    Article
  9. Article
  10. Article
  11. Article
  12. The Utilisation of Hydrogels for iPSC-Cardiomyocyte Research.International journal of molecular sciences · 2023
    Review
  13. Engineering approaches for cardiac organoid formation and their characterization.Translational research : the journal of laboratory and clinical medicine · 2022
    Review
  14. Latest Advances in 3D Bioprinting of Cardiac Tissues.Advanced materials technologies · 2022
    Article
  15. Review
  16. Article
  17. Reconstructing the heart using iPSCs: Engineering strategies and applications.Journal of molecular and cellular cardiology · 2021
    Review
  18. Article
  19. Review
  20. Article
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

4 authors at 3 institutions in 4 countries.

Kareen L K CoulombeCenter for Cardiovascular Biology.
Vivek K Bajpai
Stelios T Andreadis
Charles E Murry
Cardiovascular Research Center · BRBuffalo State University · USUniversity at Buffalo, State University of New York · US

Funding

Self Renewal and Differentiation of Human Embryonic Stem CellsP01GM081619 · NIGMS · UNIVERSITY OF WASHINGTON · PI REH, THOMAS A · 2007 to 2017
$20.6M
Vascularization and Growth of Human Myocardial GraftsP01HL094374 · NHLBI · UNIVERSITY OF WASHINGTON · PI MINAMI, ELINA · 2010 to 2014
$14.5M
Expansion of cardiac and hematopoietic progenitors by Wnt and NotchU01HL100405 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI EPSTEIN, JONATHAN A., MORRISEY, EDWARD E · 2009 to 2015
$8.1M
Cell-Based Cardiac RepairR01HL084642 · NHLBI · UNIVERSITY OF WASHINGTON · PI MURRY, CHARLES E · 2007 to 2014
$4.9M
Stem Cells for Vascular Tissue EngineeringR01HL086582 · NHLBI · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI ANDREADIS, STELIOS THEOHARIS · 2008 to 2017
$3.1M
Regenerating the Heart with Engineered Human Cardiac TissueR00HL115123 · NHLBI · BROWN UNIVERSITY · PI COULOMBE, KAREEN LK · 2014 to 2016
$747k
Regenerating the Heart with Engineered Human Cardiac TissueK99HL115123 · NHLBI · UNIVERSITY OF WASHINGTON · PI COULOMBE, KAREEN LK · 2012 to 2013
$144k
NHLBI NIH HHS K99 HL115123NHLBI NIH HHS P01 HL094374NHLBI NIH HHS R00 HL115123NHLBI NIH HHS R01 HL084642NHLBI NIH HHS R01 HL086582NHLBI NIH HHS R01HL086582NHLBI NIH HHS U01 HL100405NIGMS NIH HHS P01 GM081619NIGMS NIH HHS P01 GM81619
6 · The paper itself

Abstract

Heart disease is the leading cause of morbidity and mortality worldwide, and regenerative therapies that replace damaged myocardium could benefit millions of patients annually. The many cell types in the heart, including cardiomyocytes, endothelial cells, vascular smooth muscle cells, pericytes, and cardiac fibroblasts, communicate via intercellular signaling and modulate each other's function. Although much progress has been made in generating cells of the cardiovascular lineage from human pluripotent stem cells, a major challenge now is creating the tissue architecture to integrate a microvascular circulation and afferent arterioles into such an engineered tissue. Recent advances in cardiac and vascular tissue engineering will move us closer to the goal of generating functionally mature tissue. Using the biology of the myocardium as the foundation for designing engineered tissue and addressing the challenges to implantation and integration, we can bridge the gap from bench to bedside for a clinically tractable engineered cardiac tissue.

Indexed as

AnimalsCell CommunicationCell LineageCoculture TechniquesEndothelial CellsFibroblastsHeartHeart DiseasesHumansMiceMicrocirculationMuscle, Smooth, VascularMyocardiumNeovascularization, PathologicPluripotent Stem CellsRatscardiac tissue engineeringcardiovascular regenerative medicinecoronary artery diseaseheart failuremicrovessel engineeringmyocardial infarctionstem cells

Identifiers

PMID24819474
PMCPMC4213953
OpenAlexW2097999426

What OpenQuestion holds

Textmetadata
LicenceTDM
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.