Evidence map›Paper›PMID 32700830›Full record

ArticleStem cells translational medicine2020

CRISPR/Cas9-mediated introduction of the sodium/iodide symporter gene enables noninvasive in vivo tracking of induced pluripotent stem cell-derived cardiomyocytes.

John W Ostrominski, Ravi Chandra Yada, Noriko Sato, Michael Klein, Ksenia Blinova, Dakshesh Patel, Racquel Valadez, Maryknoll Palisoc, Stefania Pittaluga, Kah-Whye Peng and 11 more

Open access · goldAbstract read
In one paragraph

Article in Stem cells translational medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.7field-weighted citation impact, top 33% 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

14 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
  2. Article
  3. Gene editing enables non-invasiveMolecular therapy. Methods & clinical development · 2025
    Article
  4. In vivo tracking of ex-vivo-generatedMolecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
  5. Article
  6. Article
  7. Frontiers in cardiovascular medicine · 2023
    Article
  8. Genome Editing and Cardiac Regeneration.Advances in experimental medicine and biology · 2023
    Article
  9. Review
  10. Evaluation of [Molecular imaging · 2022
    Article
  11. Review
  12. Review
  13. Review
  14. Article
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

21 authors at 7 institutions in 1 country.

John W OstrominskiTranslational Stem Cell Biology Branch, National Heart, Lung and Blood Institute (NHLBI), National Institutes of Health (NIH), Bethesda, Maryland, USA.
Ravi Chandra YadaTranslational Stem Cell Biology Branch, National Heart, Lung and Blood Institute (NHLBI), National Institutes of Health (NIH), Bethesda, Maryland, USA.
Noriko SatoMolecular Imaging Program, Laboratory of Cellular Therapeutics, National Cancer Institute (NCI), NIH, Bethesda, Maryland, USA.
Michael KleinDivision of Cardiology, Uniformed Services University of the Health Sciences, Bethesda, Maryland, USA.
Ksenia BlinovaOffice of Science and Engineering Laboratories, Center for Devices and Radiological Health, US Food and Drug Administration, Silver Spring, Maryland, USA.
Dakshesh PatelOffice of Science and Engineering Laboratories, Center for Devices and Radiological Health, US Food and Drug Administration, Silver Spring, Maryland, USA.
Racquel ValadezLaboratory of Pathology, Center for Cancer Research, NCI, NIH, Bethesda, Maryland, USA.
Maryknoll PalisocLaboratory of Pathology, Center for Cancer Research, NCI, NIH, Bethesda, Maryland, USA.
Stefania PittalugaLaboratory of Pathology, Center for Cancer Research, NCI, NIH, Bethesda, Maryland, USA.
Kah-Whye PengDepartment of Molecular Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Hong SanAnimal Surgery and Resources Core, NHLBI, NIH, Bethesda, Maryland, USA.
Yongshun LiniPSC Core, NHLBI, NIH, Bethesda, Maryland, USA.
Falguni BasuliChemistry and Synthesis Center, NHLBI, NIH, Bethesda, Maryland, USA.
Xiang ZhangChemistry and Synthesis Center, NHLBI, NIH, Bethesda, Maryland, USA.
Rolf E SwensonChemistry and Synthesis Center, NHLBI, NIH, Bethesda, Maryland, USA.
Mark HaigneyDivision of Cardiology, Uniformed Services University of the Health Sciences, Bethesda, Maryland, USA.
Peter L ChoykeMolecular Imaging Program, Laboratory of Cellular Therapeutics, National Cancer Institute (NCI), NIH, Bethesda, Maryland, USA.
Jizhong ZouiPSC Core, NHLBI, NIH, Bethesda, Maryland, USA.
Manfred BoehmLaboratory of Cardiovascular Regenerative Medicine, NHLBI, NIH, Bethesda, Maryland, USA.
So Gun HongTranslational Stem Cell Biology Branch, National Heart, Lung and Blood Institute (NHLBI), National Institutes of Health (NIH), Bethesda, Maryland, USA.ORCID 0000-0002-3538-5444
Cynthia E DunbarTranslational Stem Cell Biology Branch, National Heart, Lung and Blood Institute (NHLBI), National Institutes of Health (NIH), Bethesda, Maryland, USA.ORCID 0000-0002-7645-838X
National Heart Lung and Blood Institute · USCenter for Cancer Research · USCenter for Devices and Radiological Health · USNational Cancer Institute · USNational Institutes of Health · USUniformed Services University of the Health Sciences · USMayo Clinic · US

Funding

Retroviral Mediated Gene Transfer Into Primate Hematopoietic CellsZIAHL002338 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI HONG, SO GUN · 2019 to 2025
$26.3M
NHLBI iPSC Core FacilityZICHL006145 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI ZOU, JIZHONG · 2012 to 2025
$23.3M
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

Techniques that enable longitudinal tracking of cell fate after myocardial delivery are imperative for optimizing the efficacy of cell-based cardiac therapies. However, these approaches have been underutilized in preclinical models and clinical trials, and there is considerable demand for site-specific strategies achieving long-term expression of reporter genes compatible with safe noninvasive imaging. In this study, the rhesus sodium/iodide symporter (NIS) gene was incorporated into rhesus macaque induced pluripotent stem cells (RhiPSCs) via CRISPR/Cas9. Cardiomyocytes derived from NIS-RhiPSCs (NIS-RhiPSC-CMs) exhibited overall similar morphological and electrophysiological characteristics compared to parental control RhiPSC-CMs at baseline and with exposure to physiological levels of sodium iodide. Mice were injected intramyocardially with 2 million NIS-RhiPSC-CMs immediately following myocardial infarction, and serial positron emission tomography/computed tomography was performed with

Indexed as

AnimalsCell DifferentiationCRISPR-Cas SystemsDisease Models, AnimalHumansInduced Pluripotent Stem CellsMiceMyocytes, CardiacSodium-Iodide SymportersSymportersTransfectionSodium-Iodide SymportersSymporterscardiomyocytesCRISPR/Cas9electrophysiologyimagingin vivo trackingiPSCsNISPETrhesus macaquesodium iodide symporter

Identifiers

PMID32700830
PMCPMC7519772
OpenAlexW3044027545

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.