Evidence map›Paper›PMID 31173076›Full record

ArticleCardiovascular research2020

A human embryonic stem cell reporter line for monitoring chemical-induced cardiotoxicity.

Su-Yi Tsai, Zaniar Ghazizadeh, Hou-Jun Wang, Sadaf Amin, Francis A Ortega, Zohreh Sadat Badieyan, Zi-Ting Hsu, Miriam Gordillo, Ritu Kumar, David J Christini and 2 more

Erratum issuedOpen access · greenAbstract readVideo-Audio Media
In one paragraph

Article in Cardiovascular research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

16 citing papers in PubMed, 20 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 2 institutions in 2 countries.

Su-Yi TsaiDepartment of Life Science, National Taiwan University, Taipei 10617, Taiwan.
Zaniar GhazizadehDepartment of Surgery, Weill Cornell Medical College, New York, NY 10065, USA.
Hou-Jun WangDepartment of Life Science, National Taiwan University, Taipei 10617, Taiwan.
Sadaf AminDepartment of Surgery, Weill Cornell Medical College, New York, NY 10065, USA.
Francis A OrtegaPhysiology, Biophysics, and Systems Biology Graduate Program, Weill Cornell Medical College, New York, NY 10065, USA.
Zohreh Sadat BadieyanDepartment of Surgery, Weill Cornell Medical College, New York, NY 10065, USA.
Zi-Ting HsuDepartment of Life Science, National Taiwan University, Taipei 10617, Taiwan.
Miriam GordilloDepartment of Surgery, Weill Cornell Medical College, New York, NY 10065, USA.
Ritu KumarDepartment of Surgery, Weill Cornell Medical College, New York, NY 10065, USA.
David J ChristiniPhysiology, Biophysics, and Systems Biology Graduate Program, Weill Cornell Medical College, New York, NY 10065, USA.
Todd EvansDepartment of Surgery, Weill Cornell Medical College, New York, NY 10065, USA.
Shuibing ChenDepartment of Surgery, Weill Cornell Medical College, New York, NY 10065, USA.
Cornell University · USNational Taiwan University · TW

Funding

A Gata456 Pipeline of DiscoveryR35HL135778 · NHLBI · WEILL MEDICAL COLL OF CORNELL UNIV · PI EVANS, TODD R · 2017 to 2023
$5.7M
NHLBI NIH HHS R35 HL135778
6 · The paper itself

Abstract

aimsHuman embryonic stem cells (hESCs) can be used to generate scalable numbers of cardiomyocytes (CMs) for studying cardiac biology, disease modelling, drug screens, and potentially for regenerative therapies. A fluorescence-based reporter line will significantly enhance our capacities to visualize the derivation, survival, and function of hESC-derived CMs. Our goal was to develop a reporter cell line for real-time monitoring of live hESC-derived CMs. METHODS AND

resultsWe used CRISPR/Cas9 to knock a mCherry reporter gene into the MYH6 locus of hESC lines, H1 and H9, enabling real-time monitoring of the generation of CMs. MYH6:mCherry+ cells express atrial or ventricular markers and display a range of cardiomyocyte action potential morphologies. At 20 days of differentiation, MYH6:mCherry+ cells show features characteristic of human CMs and can be used successfully to monitor drug-induced cardiotoxicity and oleic acid-induced cardiac arrhythmia.

conclusionWe created two MYH6:mCherry hESC reporter lines and documented the application of these lines for disease modelling relevant to cardiomyocyte biology.

Indexed as

Cell DifferentiationAction PotentialsArrhythmias, CardiacBiomarkersCardiac MyosinsCardiotoxicityCell LineCRISPR-Cas SystemsDoxorubicinGene Knock-In TechniquesGenes, ReporterHeart DiseasesHuman Embryonic Stem CellsHumansLuminescent ProteinsMyocytes, CardiacBiomarkersCardiac MyosinsDoxorubicinLuminescent ProteinsMYH6 protein, humanMyosin Heavy ChainsOleic AcidRed Fluorescent ProteinCardiomyocyteCardiotoxicity testingDisease modelhESC reporterMYH6

Identifiers

PMID31173076
PMCPMC7252441
OpenAlexW2963461871

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.