Evidence map›Paper›PMID 26028533›Full record

ArticleStem cell reports2015

Efficient Generation of Cardiac Purkinje Cells from ESCs by Activating cAMP Signaling.

Su-Yi Tsai, Karen Maass, Jia Lu, Glenn I Fishman, Shuibing Chen, Todd Evans

Open access · goldAbstract read
In one paragraph

Article in Stem cell reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 20% 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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 36 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Heart rhythmFrontiers in cardiovascular medicine · 2024
    Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. hiPSC-Derived Cardiac Tissue for Disease Modeling and Drug Discovery.International journal of molecular sciences · 2020
    Review
  15. Article
  16. TRANSCRIPTIONAL REGULATION OF THE CARDIAC CONDUCTION SYSTEM.Transactions of the American Clinical and Climatological Association · 2020
    Article
  17. Article
  18. Article
  19. Review
  20. Review
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

6 authors at 2 institutions in 1 country.

Su-Yi TsaiDepartment of Surgery, Weill Cornell Medical College, New York, NY 10065, USA.
Karen MaassLeon H. Charney Division of Cardiology, New York University School of Medicine, New York, NY 10016, USA.
Jia LuLeon H. Charney Division of Cardiology, New York University School of Medicine, New York, NY 10016, USA.
Glenn I FishmanLeon H. Charney Division of Cardiology, New York University School of Medicine, New York, NY 10016, USA. Electronic address: glenn.fishman@nyumc.org.
Shuibing ChenDepartment of Surgery, Weill Cornell Medical College, New York, NY 10065, USA. Electronic address: shc2034@med.cornell.edu.
Todd EvansDepartment of Surgery, Weill Cornell Medical College, New York, NY 10065, USA. Electronic address: tre2003@med.cornell.edu.
Cornell University · USNew York University · US

Funding

Purkinje Cells and Arrhythmia MechanismsR01HL105983 · NHLBI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI FISHMAN, GLENN I · 2011 to 2019
$5.2M
A molecular pathway controlling cardiomyocyte specification.R01HL111400 · NHLBI · WEILL MEDICAL COLL OF CORNELL UNIV · PI EVANS, TODD R · 2012 to 2016
$2.1M
NHLBI NIH HHS HL105983NHLBI NIH HHS HL111400NHLBI NIH HHS R01 HL105983NHLBI NIH HHS R01 HL111400
6 · The paper itself

Abstract

Dysfunction of the specialized cardiac conduction system (CCS) is associated with life-threatening arrhythmias. Strategies to derive CCS cells, including rare Purkinje cells (PCs), would facilitate models for mechanistic studies and drug discovery and also provide new cellular materials for regenerative therapies. A high-throughput chemical screen using CCS:lacz and Contactin2:egfp (Cntn2:egfp) reporter embryonic stem cell (ESC) lines was used to discover a small molecule, sodium nitroprusside (SN), that efficiently promotes the generation of cardiac cells that express gene profiles and generate action potentials of PC-like cells. Imaging and mechanistic studies suggest that SN promotes the generation of PCs from cardiac progenitors initially expressing cardiac myosin heavy chain and that it does so by activating cyclic AMP signaling. These findings provide a strategy to derive scalable PCs, along with insight into the ontogeny of CCS development.

Indexed as

Action PotentialsCatechinCell DifferentiationCell LineCyclic AMPEmbryonic Stem CellsHumansMyocytes, CardiacMyosin Heavy ChainsNitroprussideOleic AcidPhenotypePurkinje CellsReal-Time Polymerase Chain ReactionSignal TransductionTranscriptomeCatechinCyclic AMPMyosin Heavy ChainsNitroprussideOleic Acid

Identifiers

PMID26028533
PMCPMC4471825
OpenAlexW1927138702

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.