Evidence map›Paper›PMID 28875579›Full record

ArticleJournal of tissue engineering and regenerative medicine2018

A cardiac patch from aligned microvessel and cardiomyocyte patches.

Jeremy A Schaefer, Pilar A Guzman, Sonja B Riemenschneider, Timothy J Kamp, Robert T Tranquillo

Open access · bronzeAbstract read
In one paragraph

Article in Journal of tissue engineering and regenerative medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 2 pooled it
6.0field-weighted citation impact, top 3% 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

41 citing papers in PubMed, 2 syntheses or guidelines pooled it, 63 citations in OpenAlex.

  1. Engineering the maturation of stem cell-derived cardiomyocytes.Frontiers in bioengineering and biotechnology · 2023
    Pooled it
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  17. Human Endothelial Colony-Forming Cells.Cold Spring Harbor perspectives in medicine · 2022
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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

5 authors at 2 institutions in 1 country.

Jeremy A SchaeferDepartment of Biomedical Engineering, University of Minnesota, Minneapolis, MN, USA.ORCID 0000-0003-1046-4581
Pilar A GuzmanIntegrative Biology and Physiology, University of Minnesota, Minneapolis, MN, USA.
Sonja B RiemenschneiderDepartment of Chemical Engineering and Materials Science, University of Minnesota, Minneapolis, MN, USA.
Timothy J KampDepartment of Medicine and Public Health, University of Wisconsin-Madison, Madison, WI, USA.
Robert T TranquilloDepartment of Biomedical Engineering, University of Minnesota, Minneapolis, MN, USA.ORCID 0000-0003-4668-6135
University of Minnesota · USUniversity of Wisconsin–Madison · US

Funding

Perfusable and beating engineered myocardium from human progenitor cells based onR01HL108670 · NHLBI · UNIVERSITY OF MINNESOTA · PI TRANQUILLO, ROBERT T · 2011 to 2014
$2.9M
NHLBI NIH HHS R01 HL108670
6 · The paper itself

Abstract

Cardiac tissue engineering aims to produce replacement tissue patches in the lab to replace or treat infarcted myocardium. However, current patches lack preformed microvascularization and are therefore limited in thickness and force production. In this study, we sought to assess whether a bilayer patch composed of a layer made from human induced pluripotent stem cell-derived cardiomyocytes and a microvessel layer composed of self-assembled human blood outgrowth endothelial cells and pericytes was capable of engrafting on the epicardial surface of a nude rat infarct model and becoming perfused by the host 4 weeks after acute implantation. The bilayer configuration was found to increase the twitch force production, improve human induced pluripotent stem cell-derived cardiomyocyte survival and maturation, and increase patent microvessel lumens compared with time-matched single layer controls after 2 weeks of in vitro culture. Upon implantation, the patch microvessels sprouted into the cardiomyocyte layer of the patch and inosculated with the host vasculature as evidenced by species-specific perfusion labels and erythrocyte staining. Our results demonstrate that the added microvessel layer of a bilayer patch substantially improves in vitro functionality and that the bilayer patch is capable of engraftment with rapid microvessel inosculation on injured myocardium. The bilayer format will allow for scaling up in size through the addition of layers to obtain thicker tissues generating greater force in the future.

Indexed as

AnimalsFemaleHeart VentriclesHumansImplants, ExperimentalInduced Pluripotent Stem CellsMicrovesselsMyocardiumMyocytes, CardiacPerfusionRats, NudeTissue ScaffoldsVascular Remodelingcardiomyocytecardiomyocyte maturationengineered microvesselengineered myocardiuminduced pluripotent stem cell-derived cardiomyocytetissue engineering

Identifiers

PMID28875579
PMCPMC5814344
OpenAlexW2752215888

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.