Evidence map›Paper›PMID 29651156›Full record

ArticleScientific reports2018

Efficient differentiation of cardiomyocytes and generation of calcium-sensor reporter lines from nonhuman primate iPSCs.

Yongshun Lin, Huimin Liu, Michael Klein, John Ostrominski, So Gun Hong, Ravi Chandra Yada, Guibin Chen, Keron Navarengom, Robin Schwartzbeck, Hong San and 8 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

20 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Article
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  6. Article
  7. Review
  8. Genome Editing and Cardiac Regeneration.Advances in experimental medicine and biology · 2023
    Article
  9. Article
  10. Sympathetic Neurons Regulate Cardiomyocyte Maturation in Culture.Frontiers in cell and developmental biology · 2022
    Article
  11. Article
  12. Article
  13. Engineering and Assessing Cardiac Tissue Complexity.International journal of molecular sciences · 2021
    Review
  14. Review
  15. Article
  16. Article
  17. Review
  18. Review
  19. Article
  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

18 authors at 5 institutions in 2 countries.

Yongshun LiniPSC Core, National Heart, Lung, and Blood Institute (NHLBI), National Institutes of Health (NIH), Bethesda, Maryland, USA.
Huimin LiuiPSC Core, National Heart, Lung, and Blood Institute (NHLBI), National Institutes of Health (NIH), Bethesda, Maryland, USA.
Michael KleinUniformed Services University of Health Sciences, Bethesda, Maryland, USA.
John OstrominskiHematology Branch, NHLBI, NIH, Bethesda, Maryland, USA.
So Gun HongHematology Branch, NHLBI, NIH, Bethesda, Maryland, USA.
Ravi Chandra YadaHematology Branch, NHLBI, NIH, Bethesda, Maryland, USA.
Guibin ChenLaboratory of Cardiovascular Regenerative Medicine, Center for Molecular Medicine, NHLBI, NIH, Bethesda, Maryland, USA.
Keron NavarengomLaboratory of Cardiovascular Regenerative Medicine, Center for Molecular Medicine, NHLBI, NIH, Bethesda, Maryland, USA.
Robin SchwartzbeckLaboratory of Cardiovascular Regenerative Medicine, Center for Molecular Medicine, NHLBI, NIH, Bethesda, Maryland, USA.
Hong SanGenome Techology Branch, National Human Genome Research Institute, NIH, Bethesda, Maryland, USA.
Zu-Xi YuPathology Core, NHLBI, NIH, Bethesda, Maryland, USA.
Chengyu LiuTransgenic Core, NHLBI, NIH, Bethesda, Maryland, USA.
Kaari LinaskiPSC Core, National Heart, Lung, and Blood Institute (NHLBI), National Institutes of Health (NIH), Bethesda, Maryland, USA.
Jeanette BeersiPSC Core, National Heart, Lung, and Blood Institute (NHLBI), National Institutes of Health (NIH), Bethesda, Maryland, USA.
Lugui QiuState Key Laboratory of Experimental Hematology, Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Science and Peking Union Medical College, Tianjin, China.
Cynthia E DunbarHematology Branch, NHLBI, NIH, Bethesda, Maryland, USA.
Manfred BoehmLaboratory of Cardiovascular Regenerative Medicine, Center for Molecular Medicine, NHLBI, NIH, Bethesda, Maryland, USA.
Jizhong ZouiPSC Core, National Heart, Lung, and Blood Institute (NHLBI), National Institutes of Health (NIH), Bethesda, Maryland, USA. zouj2@nhlbi.nih.gov.ORCID 0000-0003-1021-0549
National Institutes of Health · USNational Heart Lung and Blood Institute · USInstitute of Hematology & Blood Diseases Hospital · CNNational Human Genome Research Institute · USUniformed Services University of the Health Sciences · US

Funding

NHLBI Animal Program DivisionZIGHL006020 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI CLARK, TANNIA · 2009 to 2025
$47.3M
Transgenic CoreZICHL005907 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI LIU, CHENGYU · 2010 to 2025
$25.8M
NHLBI iPSC Core FacilityZICHL006145 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI ZOU, JIZHONG · 2012 to 2025
$23.3M
Vascular remodeling in patients with rare genetic disordersZIAHL006077 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI BOEHM, MANFRED · 2010 to 2025
$22.9M
iPS-technology and patient specific disease modelsZIAHL006079 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI BOEHM, MANFRED · 2010 to 2025
$14.4M
Pathology CoreZICHL005904 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI YU, ZU XI · 2010 to 2023
$11.6M
The rhesus macaque as a preclinical model for induced pluripotent stem cellsZIAHL006062 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI DUNBAR, CYNTHIA E · 2010 to 2024
$8.2M
6 · The paper itself

Abstract

Nonhuman primate (NHP) models are more predictive than rodent models for developing induced pluripotent stem cell (iPSC)-based cell therapy, but robust and reproducible NHP iPSC-cardiomyocyte differentiation protocols are lacking for cardiomyopathies research. We developed a method to differentiate integration-free rhesus macaque iPSCs (RhiPSCs) into cardiomyocytes with >85% purity in 10 days, using fully chemically defined conditions. To enable visualization of intracellular calcium flux in beating cardiomyocytes, we used CRISPR/Cas9 to stably knock-in genetically encoded calcium indicators at the rhesus AAVS1 safe harbor locus. Rhesus cardiomyocytes derived by our stepwise differentiation method express signature cardiac markers and show normal electrochemical coupling. They are responsive to cardiorelevant drugs and can be successfully engrafted in a mouse myocardial infarction model. Our approach provides a powerful tool for generation of NHP iPSC-derived cardiomyocytes amenable to utilization in basic research and preclinical studies, including in vivo tissue regeneration models and drug screening.

Indexed as

Founder EffectAnimalsBiomarkersCalciumCardiovascular AgentsCell DifferentiationCell LineCRISPR-Cas SystemsDependovirusDisease Models, AnimalFluorescenceGene ExpressionGene Knock-In TechniquesGenes, ReporterGenetic LociGenetic VectorsBiomarkersCalciumCardiovascular AgentsNanog Homeobox ProteinOctamer Transcription Factor-3stage-specific embryonic antigen-4Stage-Specific Embryonic Antigens

Identifiers

PMID29651156
PMCPMC5897327
OpenAlexW2805189781

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.