Evidence map›Paper›PMID 37540743›Full record

ArticleScience advances2023

Nanowired human cardiac organoid transplantation enables highly efficient and effective recovery of infarcted hearts.

Yu Tan, Robert C Coyle, Ryan W Barrs, Sophia E Silver, Mei Li, Dylan J Richards, Yiliang Lin, Yuanwen Jiang, Hongjun Wang, Donald R Menick and 3 more

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
15.6field-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

34 citing papers in PubMed, 49 citations in OpenAlex.

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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

13 authors at 4 institutions in 1 country.

Yu TanBioengineering Department, Clemson University, Clemson, SC 29634, USA.ORCID 0000-0002-0608-9179
Robert C CoyleBioengineering Department, Clemson University, Clemson, SC 29634, USA.
Ryan W BarrsBioengineering Department, Clemson University, Clemson, SC 29634, USA.ORCID 0000-0001-7747-1941
Sophia E SilverBioengineering Department, Clemson University, Clemson, SC 29634, USA.ORCID 0000-0003-0718-591X
Mei LiBioengineering Department, Clemson University, Clemson, SC 29634, USA.
Dylan J RichardsBioengineering Department, Clemson University, Clemson, SC 29634, USA.
Yiliang LinDepartment of Chemistry, The James Franck Institute and the Institute for Biophysical Dynamics, The University of Chicago, Chicago, IL 60637, USA.ORCID 0000-0001-9403-9464
Yuanwen JiangDepartment of Chemistry, The James Franck Institute and the Institute for Biophysical Dynamics, The University of Chicago, Chicago, IL 60637, USA.
Hongjun WangDepartment of Surgery, Medical University of South Carolina, Charleston, SC 29425, USA.ORCID 0000-0001-7421-1917
Donald R MenickDivision of Cardiology, Department of Medicine, Gazes Cardiac Research Institute, Ralph H. Johnson Veterans Affairs Medical Center, Medical University of South Carolina, Charleston, SC 29425, USA.
Kristine Deleon-PennellDivision of Cardiology, Department of Medicine, Gazes Cardiac Research Institute, Ralph H. Johnson Veterans Affairs Medical Center, Medical University of South Carolina, Charleston, SC 29425, USA.ORCID 0000-0002-9647-6112
Bozhi TianDepartment of Chemistry, The James Franck Institute and the Institute for Biophysical Dynamics, The University of Chicago, Chicago, IL 60637, USA.ORCID 0000-0003-0593-0023
Ying MeiBioengineering Department, Clemson University, Clemson, SC 29634, USA.ORCID 0000-0002-8508-4076
Clemson University · USUniversity of Chicago · USMedical University of South Carolina · USRalph H. Johnson VA Medical Center · US

Funding

Subproject Title: Clinical Research Education, Mentoring and Career Development CoreU54GM104941 · NIGMS · UNIVERSITY OF DELAWARE · PI Megan M Wenner · 2013 to 2026
$60.5M
Targeted Nano-therapeutics for Neural RegenerationP20GM103444 · NIGMS · CLEMSON UNIVERSITY · PI VYAVAHARE, NAREN R · 2012 to 2018
$14.9M
Training In Cardiovascular Physiology & PharmacologyT32HL007444 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Ju Chen, Robert Scott Ross · 1985 to 2026
$11.1M
TRAINING TO IMPROVE CARDIOVASCULAR THERAPIEST32HL007260 · NHLBI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI MENICK, DONALD R. · 1985 to 2021
$11.1M
SC COBRE for Developmentally Based Cardiovascular DiseasesP30GM103342 · NIGMS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI MARKWALD, ROGER R · 2012 to 2016
$5.5M
UCSD PRIDE Faculty Development Program in Cardiovascular SciencesR25HL145817 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Robert Scott Ross, Joann Trejo · 2019 to 2026
$3.3M
Nanowired human cardiac spheroids for heart repairR01HL133308 · NHLBI · CLEMSON UNIVERSITY · PI MEI, YING · 2017 to 2020
$1.5M
Leveraging the HIF-alpha pathway to improve the engraftment and therapeutic efficacy of human nanowired cardiac organoidsF31HL156541 · NHLBI · CLEMSON UNIVERSITY · PI BARRS, RYAN W · 2021 to 2023
$106k
Improving hiPSC cardiomyocyte engraftment and integration with nanowired human cardiac organoidsF31HL145979 · NHLBI · CLEMSON UNIVERSITY · PI COYLE, ROBERT · 2019 to 2020
$73k
Regulatroy Role of HDAC in Post-MI Ventricular RemodelingI01BX002327 · VA · RALPH H JOHNSON VA MEDICAL CENTER · PI MENICK, DONALD R. · 2015 to 2023
–
BLRD VA I01 BX002327NHLBI NIH HHS F31 HL145979NHLBI NIH HHS F31 HL156541NHLBI NIH HHS R01 HL133308NHLBI NIH HHS R25 HL145817NHLBI NIH HHS T32 HL007260NHLBI NIH HHS T32 HL007444NIGMS NIH HHS P20 GM103444NIGMS NIH HHS P30 GM103342NIGMS NIH HHS U54 GM104941
6 · The paper itself

Abstract

Human cardiac organoids hold remarkable potential for cardiovascular disease modeling and human pluripotent stem cell-derived cardiomyocyte (hPSC-CM) transplantation. Here, we show cardiac organoids engineered with electrically conductive silicon nanowires (e-SiNWs) significantly enhance the therapeutic efficacy of hPSC-CMs to treat infarcted hearts. We first demonstrated the biocompatibility of e-SiNWs and their capacity to improve cardiac microtissue engraftment in healthy rat myocardium. Nanowired human cardiac organoids were then engineered with hPSC-CMs, nonmyocyte supporting cells, and e-SiNWs. Nonmyocyte supporting cells promoted greater ischemia tolerance of cardiac organoids, and e-SiNWs significantly improved electrical pacing capacity. After transplantation into ischemia/reperfusion-injured rat hearts, nanowired cardiac organoids significantly improved contractile development of engrafted hPSC-CMs, induced potent cardiac functional recovery, and reduced maladaptive left ventricular remodeling. Compared to contemporary studies with an identical injury model, greater functional recovery was achieved with a 20-fold lower dose of hPSC-CMs, revealing therapeutic synergy between conductive nanomaterials and human cardiac organoids for efficient heart repair.

Indexed as

Induced Pluripotent Stem CellsMyocardial InfarctionAnimalsCell DifferentiationHumansIschemiaMyocardiumOrganoidsRats

Identifiers

PMID37540743
PMCPMC10403216
OpenAlexW4385565566

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.