Evidence map›Paper›PMID 28500172›Full record

ArticleCirculation. Arrhythmia and electrophysiology2017

Induced Pluripotent Stem Cell-Derived Cardiomyocytes Provide In Vivo Biological Pacemaker Function.

Samuel Chauveau, Evgeny P Anyukhovsky, Meital Ben-Ari, Shulamit Naor, Ya-Ping Jiang, Peter Danilo, Tania Rahim, Stephanie Burke, Xiaoliang Qiu, Irina A Potapova and 5 more

Open access · greenAbstract read
In one paragraph

Article in Circulation. Arrhythmia and electrophysiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

42 citing papers in PubMed, 74 citations in OpenAlex.

  1. Article
  2. Review
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  7. Heart rhythmFrontiers in cardiovascular medicine · 2024
    Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Recombinant Adeno-Associated Viral Vector-Mediated Gene Transfer ofInternational journal of molecular sciences · 2022
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Implementing Biological Pacemakers: Design Criteria for Successful.Circulation. Arrhythmia and electrophysiology · 2021
    Review
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 2 institutions in 6 countries.

Samuel ChauveauFor the author affiliations, please see the Appendix.
Evgeny P AnyukhovskyFor the author affiliations, please see the Appendix.
Meital Ben-AriFor the author affiliations, please see the Appendix.
Shulamit NaorFor the author affiliations, please see the Appendix.
Ya-Ping JiangFor the author affiliations, please see the Appendix.
Peter DaniloFor the author affiliations, please see the Appendix.
Tania RahimFor the author affiliations, please see the Appendix.
Stephanie BurkeFor the author affiliations, please see the Appendix.
Xiaoliang QiuFor the author affiliations, please see the Appendix.
Irina A PotapovaFor the author affiliations, please see the Appendix.
Sergey V DoroninFor the author affiliations, please see the Appendix.
Peter R BrinkFor the author affiliations, please see the Appendix.
Ofer BinahFor the author affiliations, please see the Appendix.
Ira S CohenFor the author affiliations, please see the Appendix. ira.cohen@stonybrook.edu mrr1@cumc.columbia.edu.
Michael R RosenFor the author affiliations, please see the Appendix. ira.cohen@stonybrook.edu mrr1@cumc.columbia.edu.
TiGenix (Spain) · ESApple (Israel) · IL

Funding

From human keratinocytes to biological pacemakersR01HL111401 · NHLBI · STATE UNIVERSITY NEW YORK STONY BROOK · PI COHEN, IRA S · 2012 to 2015
$2.6M
NHLBI NIH HHS R01 HL111401
6 · The paper itself

Abstract

backgroundAlthough multiple approaches have been used to create biological pacemakers in animal models, induced pluripotent stem cell-derived cardiomyocytes (iPSC-CMs) have not been investigated for this purpose. We now report pacemaker function of iPSC-CMs in a canine model. METHODS AND

resultsEmbryoid bodies were derived from human keratinocytes, their action potential characteristics determined, and their gene expression profiles and markers of differentiation identified. Atrioventricular blocked dogs were immunosuppressed, instrumented with VVI pacemakers, and injected subepicardially into the anterobasal left ventricle with 40 to 75 rhythmically contracting embryoid bodies (totaling 1.3-2×10

conclusionsiPSC-CMs can integrate into host myocardium and create a biological pacemaker. Although this is a promising development, rate and rhythm of the iPSC-CMs pacemakers remain to be optimized.

Indexed as

Biological ClocksCell DifferentiationHeart RateStem Cell TransplantationAction PotentialsAnimalsAtrioventricular BlockCardiac Pacing, ArtificialCell LineDisease Models, AnimalDogsElectrocardiographyElectrophysiologic Techniques, CardiacGene Expression ProfilingHumansInduced Pluripotent Stem CellsKruppel-Like Factor 4Kruppel-Like Transcription FactorsMYC protein, humanOctamer Transcription Factor-3POU5F1 protein, humanProto-Oncogene Proteins c-mycSOX2 protein, humanSOXB1 Transcription Factorsaction potentialsatrioventricular blockdogsembryoid bodiesmyocardium

Identifiers

PMID28500172
PMCPMC5434966
OpenAlexW2613096029

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.