Evidence map›Paper›PMID 23434590›Full record

ArticleThe Journal of clinical investigation2013

Parthenogenetic stem cells for tissue-engineered heart repair.

Michael Didié, Peter Christalla, Michael Rubart, Vijayakumar Muppala, Stephan Döker, Bernhard Unsöld, Ali El-Armouche, Thomas Rau, Thomas Eschenhagen, Alexander P Schwoerer and 21 more

Open access · greenAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed, 1 pooled it
8.1field-weighted citation impact, top 2% 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

58 citing papers in PubMed, 1 synthesis or guideline pooled it, 114 citations in OpenAlex.

  1. Guideline
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Understanding the Adult Mammalian Heart at Single-Cell RNA-Seq Resolution.Frontiers in cell and developmental biology · 2021
    Review
  12. Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Germline Stem Cells in Myocardial Regeneration - A new hope worth a delve.Journal of stem cells & regenerative medicine · 2018
    Article
  18. Article
  19. Review
  20. Engineered Heart Repair.Clinical pharmacology and therapeutics · 2017
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

31 authors at 10 institutions in 3 countries.

Michael DidiéInstitute of Pharmacology, University Medical Center Göttingen, Göttingen, Germany.
Peter Christalla
Michael Rubart
Vijayakumar Muppala
Stephan Döker
Bernhard Unsöld
Ali El-Armouche
Thomas Rau
Thomas Eschenhagen
Alexander P Schwoerer
Heimo Ehmke
Udo Schumacher
Sigrid Fuchs
Claudia Lange
Alexander Becker
Wen Tao
John A Scherschel
Mark H Soonpaa
Tao Yang
Qiong Lin
Martin Zenke
Dong-Wook Han
Hans R Schöler
Cornelia Rudolph
Doris Steinemann
Brigitte Schlegelberger
Steve Kattman
Alec Witty
Gordon Keller
Loren J Field
Wolfram-Hubertus Zimmermann
Indiana University – Purdue University Indianapolis · USUniversity of Göttingen · DEMedizinische Hochschule Hannover · DEUniversität Hamburg · DERWTH Aachen University · DEUniversity Medical Center Hamburg-Eppendorf · DEKonkuk University Medical Center · KRMax Planck Society · DEMorpho (United States) · USUniversitätsmedizin Göttingen · DE

Funding

Genetic Enhancement of Cardiac Repair with Adult Stem CellsR01HL083126 · NHLBI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI FIELD, LOREN J · 2006 to 2015
$2.9M
NHLBI NIH HHS R01 HL083126
6 · The paper itself

Abstract

Uniparental parthenotes are considered an unwanted byproduct of in vitro fertilization. In utero parthenote development is severely compromised by defective organogenesis and in particular by defective cardiogenesis. Although developmentally compromised, apparently pluripotent stem cells can be derived from parthenogenetic blastocysts. Here we hypothesized that nonembryonic parthenogenetic stem cells (PSCs) can be directed toward the cardiac lineage and applied to tissue-engineered heart repair. We first confirmed similar fundamental properties in murine PSCs and embryonic stem cells (ESCs), despite notable differences in genetic (allelic variability) and epigenetic (differential imprinting) characteristics. Haploidentity of major histocompatibility complexes (MHCs) in PSCs is particularly attractive for allogeneic cell-based therapies. Accordingly, we confirmed acceptance of PSCs in MHC-matched allotransplantation. Cardiomyocyte derivation from PSCs and ESCs was equally effective. The use of cardiomyocyte-restricted GFP enabled cell sorting and documentation of advanced structural and functional maturation in vitro and in vivo. This included seamless electrical integration of PSC-derived cardiomyocytes into recipient myocardium. Finally, we enriched cardiomyocytes to facilitate engineering of force-generating myocardium and demonstrated the utility of this technique in enhancing regional myocardial function after myocardial infarction. Collectively, our data demonstrate pluripotency, with unrestricted cardiogenicity in PSCs, and introduce this unique cell type as an attractive source for tissue-engineered heart repair.

Indexed as

Tissue EngineeringAction PotentialsAnimalsAntigens, DifferentiationCalcium SignalingCell DifferentiationCells, CulturedCell ShapeEmbryonic Stem CellsEpigenesis, GeneticGenotypeHeartHistocompatibilityHistocompatibility Antigens Class IIMiceMice, Inbred BALB CAntigens, DifferentiationHistocompatibility Antigens Class II

Identifiers

PMID23434590
PMCPMC3582145
OpenAlexW2013958285

What OpenQuestion holds

Textmetadata
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.