Evidence map›Paper›PMID 34697315›Full record

ArticleNature communications2021

Physiologic biomechanics enhance reproducible contractile development in a stem cell derived cardiac muscle platform.

Yao-Chang Tsan, Samuel J DePalma, Yan-Ting Zhao, Adela Capilnasiu, Yu-Wei Wu, Brynn Elder, Isabella Panse, Kathryn Ufford, Daniel L Matera, Sabrina Friedline and 9 more

Abstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
–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

26 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  15. Cardiac maturation.Journal of molecular and cellular cardiology · 2024
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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

19 authors.

Yao-Chang TsanDivision of Cardiovascular Medicine, University of Michigan, Ann Arbor, MI, USA.
Samuel J DePalmaDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI, USA.ORCID 0000-0001-6708-5019
Yan-Ting ZhaoDepartment of Pharmacology, University of Michigan, Ann Arbor, MI, USA.
Adela CapilnasiuDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI, USA.
Yu-Wei WuInstitute of Molecular Biology, Academia Sinica, NanKang, Taipei, Taiwan.ORCID 0000-0002-4459-087X
Brynn ElderDivision of Cardiovascular Medicine, University of Michigan, Ann Arbor, MI, USA.ORCID 0000-0001-5353-6683
Isabella PanseDivision of Cardiovascular Medicine, University of Michigan, Ann Arbor, MI, USA.
Kathryn UffordDivision of Cardiovascular Medicine, University of Michigan, Ann Arbor, MI, USA.ORCID 0000-0003-3954-2950
Daniel L MateraDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI, USA.ORCID 0000-0003-4172-7903
Sabrina FriedlineDivision of Cardiovascular Medicine, University of Michigan, Ann Arbor, MI, USA.
Thomas S O'LearyMolecular Physiology and Biophysics, University of Vermont, Burlington, VT, USA.
Nadab WubshetDepartment of Mechanical Engineering, University of Michigan, Ann Arbor, MI, USA.
Kenneth K Y HoDepartment of Mechanical Engineering, University of Michigan, Ann Arbor, MI, USA.ORCID 0000-0001-5587-8302
Michael J PrevisMolecular Physiology and Biophysics, University of Vermont, Burlington, VT, USA.
David NordslettenDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI, USA.
Lori L IsomDepartment of Pharmacology, University of Michigan, Ann Arbor, MI, USA.ORCID 0000-0002-9479-6729
Brendon M BakerDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI, USA.ORCID 0000-0002-2785-1070
Allen P LiuDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI, USA.ORCID 0000-0002-0309-7018
Adam S HelmsDivision of Cardiovascular Medicine, University of Michigan, Ann Arbor, MI, USA. adamhelm@umich.edu.ORCID 0000-0002-0234-6430

Funding

Michigan Institute for Clinical and Health Research (MICHR)UL1TR002240 · NCATS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LUMENG, JULIE C, MASHOUR, GEORGE ALEXANDER · 2017 to 2022
$54.9M
Tissue Engineering and RegenerationT32DE007057 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DAVID H. KOHN · 1985 to 2026
$17.3M
Cardiac Mechanisms of Sudden Unexpected Death in EpilepsyR01HL149363 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ISOM, LORI L., PARENT, JACK M · 2020 to 2023
$2.8M
Mechanisms governing myosin turnover and exchange in vivo.R01HL157487 · NHLBI · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI PREVIS, MICHAEL JOSEPH · 2021 to 2024
$1.8M
Genome-Engineered Stem Cell Models to Determine Disease Mechanisms in MYBPC3 Hypertrophic CardiomyopathyK08HL130455 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HELMS, ADAM S · 2016 to 2020
$818k
Molecular Modulation of Actomyosin Mechanics by Cardiac Myosin-Binding Protein CR00HL124041 · NHLBI · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI PREVIS, MICHAEL JOSEPH · 2016 to 2018
$747k
Development of a high throughput microtissue model for integrative analysis of contractile function and biomechanical stress in iPSC-derived cardiomyocytesR03HL148465 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HELMS, ADAM S · 2021 to 2022
$156k
NCATS NIH HHS UL1 TR002240NHLBI NIH HHS K08 HL130455NHLBI NIH HHS R00 HL124041NHLBI NIH HHS R01 HL149363NHLBI NIH HHS R01 HL157487NHLBI NIH HHS R03 HL148465NIDCR NIH HHS T32 DE007057
6 · The paper itself

Abstract

Human pluripotent stem cell-derived cardiomyocytes (hPSC-CMs) allow investigations in a human cardiac model system, but disorganized mechanics and immaturity of hPSC-CMs on standard two-dimensional surfaces have been hurdles. Here, we developed a platform of micron-scale cardiac muscle bundles to control biomechanics in arrays of thousands of purified, independently contracting cardiac muscle strips on two-dimensional elastomer substrates with far greater throughput than single cell methods. By defining geometry and workload in this reductionist platform, we show that myofibrillar alignment and auxotonic contractions at physiologic workload drive maturation of contractile function, calcium handling, and electrophysiology. Using transcriptomics, reporter hPSC-CMs, and quantitative immunofluorescence, these cardiac muscle bundles can be used to parse orthogonal cues in early development, including contractile force, calcium load, and metabolic signals. Additionally, the resultant organized biomechanics facilitates automated extraction of contractile kinetics from brightfield microscopy imaging, increasing the accessibility, reproducibility, and throughput of pharmacologic testing and cardiomyopathy disease modeling.

Indexed as

MyocardiumBiomechanical PhenomenaCalciumCell Culture TechniquesDimethylpolysiloxanesElectrophysiological PhenomenaGene Expression ProfilingHeartHigh-Throughput Screening AssaysHumansLab-On-A-Chip DevicesModels, CardiovascularMyocardial ContractionMyocytes, CardiacMyofibrilsPluripotent Stem CellsbaysilonCalciumDimethylpolysiloxanes

Identifiers

PMID34697315
PMCPMC8546060

What OpenQuestion holds

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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.