Evidence map›Paper›PMID 33128951›Full record

ArticleStem cell research2020

NODAL inhibition promotes differentiation of pacemaker-like cardiomyocytes from human induced pluripotent stem cells.

Sergey Yechikov, Hillary K J Kao, Che-Wei Chang, Dalyir Pretto, Xiao-Dong Zhang, Yao-Hui Sun, Regan Smithers, Padmini Sirish, Jan A Nolta, James W Chan and 2 more

Abstract read
In one paragraph

Article in Stem cell research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
–field-weighted citation impact
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

27 citing papers in PubMed.

  1. Review
  2. Coordination of cardiogenesis in vivo and in vitro.Nature reviews. Molecular cell biology · 2026
    Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Review
  14. Heart rhythmFrontiers in cardiovascular medicine · 2024
    Article
  15. Article
  16. Review
  17. Regenerative therapy · 2022
    Article
  18. Article
  19. Article
  20. A dualiScience · 2022
    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

12 authors.

Sergey YechikovDepartment of Internal Medicine, Division of Cardiovascular Medicine, University of California, Davis, Davis, CA 95817, USA; Institute for Regenerative Cures, University of California, Davis, Sacramento, CA 95817, USA.
Hillary K J KaoDepartment of Internal Medicine, Division of Cardiovascular Medicine, University of California, Davis, Davis, CA 95817, USA; Institute for Regenerative Cures, University of California, Davis, Sacramento, CA 95817, USA.
Che-Wei ChangDepartment of Pathology and Laboratory Medicine, University of California, Davis, Sacramento, CA 95817, USA.
Dalyir PrettoDepartment of Internal Medicine, Division of Cardiovascular Medicine, University of California, Davis, Davis, CA 95817, USA; Institute for Regenerative Cures, University of California, Davis, Sacramento, CA 95817, USA.
Xiao-Dong ZhangDepartment of Internal Medicine, Division of Cardiovascular Medicine, University of California, Davis, Davis, CA 95817, USA.
Yao-Hui SunDepartment of Internal Medicine, Division of Cardiovascular Medicine, University of California, Davis, Davis, CA 95817, USA; Institute for Regenerative Cures, University of California, Davis, Sacramento, CA 95817, USA.
Regan SmithersDepartment of Internal Medicine, Division of Cardiovascular Medicine, University of California, Davis, Davis, CA 95817, USA; Institute for Regenerative Cures, University of California, Davis, Sacramento, CA 95817, USA; Bridges to Stem Cell Research Program, California State University Sacramento, Sacramento, CA 95819, USA.
Padmini SirishDepartment of Internal Medicine, Division of Cardiovascular Medicine, University of California, Davis, Davis, CA 95817, USA; Department of Veterans Affairs, Northern California Health Care System, Mather, CA 95655, USA.
Jan A NoltaInstitute for Regenerative Cures, University of California, Davis, Sacramento, CA 95817, USA; Department of Hematology and Oncology, University of California, Davis, Sacramento, CA 95817, USA.
James W ChanDepartment of Pathology and Laboratory Medicine, University of California, Davis, Sacramento, CA 95817, USA.
Nipavan ChiamvimonvatDepartment of Internal Medicine, Division of Cardiovascular Medicine, University of California, Davis, Davis, CA 95817, USA; Department of Veterans Affairs, Northern California Health Care System, Mather, CA 95655, USA.
Deborah K LieuDepartment of Internal Medicine, Division of Cardiovascular Medicine, University of California, Davis, Davis, CA 95817, USA; Institute for Regenerative Cures, University of California, Davis, Sacramento, CA 95817, USA. Electronic address: dklieu@ucdavis.edu.

Funding

Functional Interactions of Cardiac Ion ChannelsR01HL085844 · NHLBI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI CHIAMVIMONVAT, NIPAVAN · 2007 to 2025
$7.3M
Training Program In Basic & Translational Cardiovascular ScienceT32HL086350 · NHLBI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Martin Cadeiras, David A. Liem · 2008 to 2026
$7.1M
Translational Study of Cardiac DysfunctionR01HL085727 · NHLBI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI CHIAMVIMONVAT, NIPAVAN, SIRISH, PADMINI · 2008 to 2022
$5.7M
Decoding the enigma of cardiac amplificationR01HL137228 · NHLBI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI CHIAMVIMONVAT, NIPAVAN · 2017 to 2020
$2.2M
Functional Regulation of Cardiac Chloride HomeostasisR56HL138392 · NHLBI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI ZHANG, XIAO-DONG · 2018 to 2018
$393k
Metabolomics study in patients post myocardial infarctionI01CX001490 · VA · VA NORTHERN CALIFORNIA HEALTH CARE SYS · PI CHIAMVIMONVAT, NIPAVAN · 2017 to 2021
–
Regulation of ion channels in the heartI01BX000576 · VA · VA NORTHERN CALIFORNIA HEALTH CARE SYS · PI CHIAMVIMONVAT, NIPAVAN · 2009 to 2019
–
BLRD VA I01 BX000576CSRD VA I01 CX001490NHLBI NIH HHS R01 HL085727NHLBI NIH HHS R01 HL085844NHLBI NIH HHS R01 HL137228NHLBI NIH HHS R56 HL138392NHLBI NIH HHS T32 HL086350
6 · The paper itself

Abstract

Directed cardiomyogenesis from human induced pluripotent stem cells (hiPSCs) has been greatly improved in the last decade but directed differentiation to pacemaking cardiomyocytes (CMs) remains incompletely understood. In this study, we demonstrated that inhibition of NODAL signaling by a specific NODAL inhibitor (SB431542) in the cardiac mesoderm differentiation stage downregulated PITX2c, a transcription factor that is known to inhibit the formation of the sinoatrial node in the left atrium during cardiac development. The resulting hiPSC-CMs were smaller in cell size, expressed higher pro-pacemaking transcription factors, TBX3 and TBX18, and exhibited pacemaking-like electrophysiological characteristics compared to control hiPSC-CMs differentiated from established Wnt-based protocol. The pacemaker-like subtype increased up to 2.4-fold in hiPSC-CMs differentiated with the addition of SB431542 relative to the control. Hence, Nodal inhibition in the cardiac mesoderm stage promoted pacemaker-like CM differentiation from hiPSCs. Improving the yield of human pacemaker-like CMs is a critical first step in the development of functional human cell-based biopacemakers.

Indexed as

Induced Pluripotent Stem CellsPacemaker, ArtificialAction PotentialsCell DifferentiationCells, CulturedHumansMyocytes, CardiacCardiogenesisDifferentiationHuman induced pluripotent stem cellsPacemakerSinoatrial node

Identifiers

PMID33128951
PMCPMC7814970

What OpenQuestion holds

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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.