Evidence map›Paper›PMID 32131688›Full record

ArticleJournal of the American Heart Association2020

Exosomes From Induced Pluripotent Stem Cell-Derived Cardiomyocytes Promote Autophagy for Myocardial Repair.

Michelle R Santoso, Gentaro Ikeda, Yuko Tada, Ji-Hye Jung, Evgeniya Vaskova, Raymond G Sierra, Cornelius Gati, Andrew B Goldstone, Daniel von Bornstaedt, Praveen Shukla and 4 more

Open access · goldAbstract read
In one paragraph

Article in Journal of the American Heart Association, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 78 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
78citing papers in PubMed, 2 pooled it
5.5field-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

78 citing papers in PubMed, 2 syntheses or guidelines pooled it, 109 citations in OpenAlex.

  1. Geographical and Ethnic Heterogeneity in Genetic Dilated Cardiomyopathies.International journal of molecular sciences · 2026
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18 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

14 authors at 4 institutions in 1 country.

Michelle R SantosoStanford Cardiovascular Institute Stanford University School of Medicine Stanford CA.
Gentaro IkedaStanford Cardiovascular Institute Stanford University School of Medicine Stanford CA.
Yuko TadaStanford Cardiovascular Institute Stanford University School of Medicine Stanford CA.
Ji-Hye JungStanford Cardiovascular Institute Stanford University School of Medicine Stanford CA.
Evgeniya VaskovaStanford Cardiovascular Institute Stanford University School of Medicine Stanford CA.
Raymond G SierraHard X-ray Department LCLS SLAC National Accelerator Laboratory Menlo Park CA.
Cornelius GatiDepartment of Structural Biology Stanford University School of Medicine Stanford CA.
Andrew B GoldstoneDepartment of Cardiothoracic Surgery Falk Building Stanford University Medical Center Stanford CA.
Daniel von BornstaedtDepartment of Structural Biology Stanford University School of Medicine Stanford CA.
Praveen ShuklaStanford Cardiovascular Institute Stanford University School of Medicine Stanford CA.
Joseph C WuStanford Cardiovascular Institute Stanford University School of Medicine Stanford CA.
Soichi WakatsukiDepartment of Structural Biology Stanford University School of Medicine Stanford CA.
Y Joseph WooDepartment of Cardiothoracic Surgery Falk Building Stanford University Medical Center Stanford CA.
Phillip C YangStanford Cardiovascular Institute Stanford University School of Medicine Stanford CA.
Cardiovascular Institute of the South · USStanford University · USStanford Medicine · USSLAC National Accelerator Laboratory · US

Funding

Cell Characterization and Imaging for Regenerative Therapies in Ischemic DiseasesUM1HL113456 · NHLBI · STANFORD UNIVERSITY · PI YANG, PHILLIP CHUNG-MING · 2012 to 2018
$3.3M
Patient Oriented Research in Cardiovascular RegenerationK24HL130553 · NHLBI · STANFORD UNIVERSITY · PI YANG, PHILLIP CHUNG-MING · 2016 to 2020
$584k
Transmission Electron MicroscopeS10RR026780 · NCRR · STANFORD UNIVERSITY · PI TALBOT, WILLIAM S · 2010 to 2010
$412k
ARRA NIH HHSNCRR NIH HHS S10 RR026780NHLBI NIH HHS K24 HL130553NHLBI NIH HHS UM1 HL113456
6 · The paper itself

Abstract

Background Induced pluripotent stem cells and their differentiated cardiomyocytes (iCMs) have tremendous potential as patient-specific therapy for ischemic cardiomyopathy following myocardial infarctions, but difficulties in viable transplantation limit clinical translation. Exosomes secreted from iCMs (iCM-Ex) can be robustly collected in vitro and injected in lieu of live iCMs as a cell-free therapy for myocardial infarction. Methods and Results iCM-Ex were precipitated from iCM supernatant and characterized by protein marker expression, nanoparticle tracking analysis, and functionalized nanogold transmission electron microscopy. iCM-Ex were then used in in vitro and in vivo models of ischemic injuries. Cardiac function in vivo was evaluated by left ventricular ejection fraction and myocardial viability measurements by magnetic resonance imaging. Cardioprotective mechanisms were studied by JC-1 (tetraethylbenzimidazolylcarbocyanine iodide) assay, immunohistochemistry, quantitative real-time polymerase chain reaction, transmission electron microscopy, and immunoblotting. iCM-Ex measured ≈140 nm and expressed CD63 and CD9. iCM and iCM-Ex microRNA profiles had significant overlap, indicating that exosomal content was reflective of the parent cell. Mice treated with iCM-Ex demonstrated significant cardiac improvement post-myocardial infarction, with significantly reduced apoptosis and fibrosis. In vitro iCM apoptosis was significantly reduced by hypoxia and exosome biogenesis inhibition and restored by treatment with iCM-Ex or rapamycin. Autophagosome production and autophagy flux was upregulated in iCM-Ex groups in vivo and in vitro. Conclusions iCM-Ex improve post-myocardial infarction cardiac function by regulating autophagy in hypoxic cardiomyoytes, enabling a cell-free, patient-specific therapy for ischemic cardiomyopathy.

Indexed as

AutophagyAnimalsApoptosisAutophagy-Related ProteinsCell HypoxiaCell LineDisease Models, AnimalExosomesFemaleFibrosisHumansInduced Pluripotent Stem CellsMice, SCIDMyocardial InfarctionMyocardiumMyocytes, CardiacAutophagy-Related ProteinsautophagyexosomesiPSCischemic cardiomyopathy

Identifiers

PMID32131688
PMCPMC7335524
OpenAlexW3009818378

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.