Evidence map›Paper›PMID 38926342›Full record

ArticleNature communications2024

Tracking single hiPSC-derived cardiomyocyte contractile function using CONTRAX an efficient pipeline for traction force measurement.

Gaspard Pardon, Alison S Vander Roest, Orlando Chirikian, Foster Birnbaum, Henry Lewis, Erica A Castillo, Robin Wilson, Aleksandra K Denisin, Cheavar A Blair, Colin Holbrook and 4 more

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Simultaneous Measurement of Contractile Force and CaSensors (Basel, Switzerland) · 2025
    Article
  5. Article
  6. Review
  7. Article
  8. Uncertainty-aware traction force microscopy.PLoS computational biology · 2025
    Article
  9. Article
  10. Article
  11. Review
  12. 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

14 authors.

Gaspard PardonDepartments of Mechanical Engineering and of Bioengineering, Stanford University, School of Engineering and School of Medicine, Stanford, CA, USA.ORCID 0000-0001-9177-1174
Alison S Vander RoestDepartments of Mechanical Engineering and of Bioengineering, Stanford University, School of Engineering and School of Medicine, Stanford, CA, USA.ORCID 0000-0001-8765-4151
Orlando ChirikianBiomolecular Science and Engineering Program, University of California, Santa Barbara, CA, USA.
Foster BirnbaumBaxter Laboratory for Stem Cell Biology, Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, USA.ORCID 0000-0002-6062-2296
Henry LewisDepartments of Mechanical Engineering and of Bioengineering, Stanford University, School of Engineering and School of Medicine, Stanford, CA, USA.
Erica A CastilloDepartments of Mechanical Engineering and of Bioengineering, Stanford University, School of Engineering and School of Medicine, Stanford, CA, USA.
Robin WilsonDepartments of Mechanical Engineering and of Bioengineering, Stanford University, School of Engineering and School of Medicine, Stanford, CA, USA.
Aleksandra K DenisinDepartments of Mechanical Engineering and of Bioengineering, Stanford University, School of Engineering and School of Medicine, Stanford, CA, USA.ORCID 0000-0002-4262-9371
Cheavar A BlairDepartments of Mechanical Engineering and of Bioengineering, Stanford University, School of Engineering and School of Medicine, Stanford, CA, USA.
Colin HolbrookBaxter Laboratory for Stem Cell Biology, Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, USA.
Kassie KoleckarBaxter Laboratory for Stem Cell Biology, Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, USA.
Alex C Y ChangBaxter Laboratory for Stem Cell Biology, Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, USA.ORCID 0000-0001-9441-4033
Helen M BlauBaxter Laboratory for Stem Cell Biology, Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, USA.ORCID 0000-0001-6503-5480
Beth L PruittDepartments of Mechanical Engineering and of Bioengineering, Stanford University, School of Engineering and School of Medicine, Stanford, CA, USA. blp@ucsb.edu.ORCID 0000-0002-4861-2124

Funding

From proteins to cells to tissues: A multi-scale assessment of biomechanical regulation by the myosin molecular motorRM1GM131981 · NIGMS · STANFORD UNIVERSITY · PI BERNSTEIN, DANIEL, MACK, DAVID LEE · 2019 to 2023
$10.3M
Dynamic Biomaterial Design to Probe the Cellular Response to Fibrotic StiffeningR01HL159340 · NHLBI · STANFORD UNIVERSITY · PI BLAU, HELEN M · 2021 to 2024
$1.6M
Modeling myosin mechanobiology towards understanding the mechanisms of hypertrophic cardiomyopathyR00HL153679 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI VANDER ROEST, ALISON SCHROER · 2023 to 2025
$851k
Modeling myosin mechanobiology towards understanding the mechanisms of hypertrophic cardiomyopathyK99HL153679 · NHLBI · STANFORD UNIVERSITY · PI VANDER ROEST, ALISON SCHROER · 2021 to 2022
$329k
The Role of Yes Associated Protein (YAP) in Hypertrophic CardiomyopathyF31HL158227 · NHLBI · UNIVERSITY OF CALIFORNIA SANTA BARBARA · PI CHIRIKIAN, ORLANDO · 2022 to 2024
$88k
American Heart Association (American Heart Association, Inc.) 13POST14480004American Heart Association (American Heart Association, Inc.) 17CSA33590101American Heart Association (American Heart Association, Inc.) 18CDA34110411American Heart Association (American Heart Association, Inc.) 18POST34080160American Heart Association (American Heart Association, Inc.) 20POST35211011Gouvernement du Canada | Canadian Institutes of Health Research (Instituts de Recherche en Santé du Canada) 201411MFE-338745-169197National Natural Science Foundation of China (National Science Foundation of China) 82070248NHLBI NIH HHS F31 HL158227NHLBI NIH HHS K99 HL153679NHLBI NIH HHS R00 HL153679NHLBI NIH HHS R01 HL159340NIGMS NIH HHS RM1 GM131981Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (Swiss National Science Foundation) P2SKP2_164954Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (Swiss National Science Foundation) P400PM_180825U.S. Department of Health & Human Services | NIH | National Heart, Lung, and Blood Institute (NHLBI) 1F31HL158227U.S. Department of Health & Human Services | NIH | National Heart, Lung, and Blood Institute (NHLBI) 1R21HL13099301U.S. Department of Health & Human Services | NIH | National Heart, Lung, and Blood Institute (NHLBI) RM1GM131981
6 · The paper itself

Abstract

Cardiomyocytes derived from human induced pluripotent stem cells (hiPSC-CMs) are powerful in vitro models to study the mechanisms underlying cardiomyopathies and cardiotoxicity. Quantification of the contractile function in single hiPSC-CMs at high-throughput and over time is essential to disentangle how cellular mechanisms affect heart function. Here, we present CONTRAX, an open-access, versatile, and streamlined pipeline for quantitative tracking of the contractile dynamics of single hiPSC-CMs over time. Three software modules enable: parameter-based identification of single hiPSC-CMs; automated video acquisition of >200 cells/hour; and contractility measurements via traction force microscopy. We analyze >4,500 hiPSC-CMs over time in the same cells under orthogonal conditions of culture media and substrate stiffnesses; +/- drug treatment; +/- cardiac mutations. Using undirected clustering, we reveal converging maturation patterns, quantifiable drug response to Mavacamten and significant deficiencies in hiPSC-CMs with disease mutations. CONTRAX empowers researchers with a potent quantitative approach to develop cardiac therapies.

Indexed as

Induced Pluripotent Stem CellsMyocardial ContractionMyocytes, CardiacSoftwareCell DifferentiationCells, CulturedHumansSingle-Cell Analysis

Identifiers

PMID38926342
PMCPMC11208611

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.