Evidence map›Paper›PMID 23007494›Full record

ArticleBiomedical microdevices2013

Sacrificial layer technique for axial force post assay of immature cardiomyocytes.

Rebecca E Taylor, Keekyoung Kim, Ning Sun, Sung-Jin Park, Joo Yong Sim, Giovanni Fajardo, Daniel Bernstein, Joseph C Wu, Beth L Pruitt

Abstract read
In one paragraph

Article in Biomedical microdevices, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

16 citing papers in PubMed, 42 citations in OpenAlex.

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  13. hiPSC Modeling of Inherited Cardiomyopathies.Current treatment options in cardiovascular medicine · 2014
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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

9 authors at 2 institutions in 1 country.

Rebecca E TaylorDepartment of Mechanical Engineering and Stanford Cardiovascular Institute, Stanford University, Stanford, CA 94305, USA.
Keekyoung Kim
Ning Sun
Sung-Jin Park
Joo Yong Sim
Giovanni Fajardo
Daniel Bernstein
Joseph C Wu
Beth L Pruitt
Stanford University · USCardiovascular Institute of the South · US

Funding

ROLE OF BETA-RECEPTOR SIGNALING IN CARDIOMYOPATHYR01HL061535 · NHLBI · STANFORD UNIVERSITY · PI BERNSTEIN, DANIEL · 2000 to 2010
$3.3M
Force Clamp Systems for Evaluation of MechanotransductionR01EB006745 · NIBIB · STANFORD UNIVERSITY · PI GOODMAN, MIRIAM B, PRUITT, BETH L · 2007 to 2014
$3.1M
09: Inducing Pluripotency with MiRNAs: New Paradigm Shif in Cell ReprogrammingDP2OD004437 · OD · STANFORD UNIVERSITY · PI WU, JOSEPH C. · 2008 to 2008
$2.4M
Nanostructuring and Molecular Imaging of Engineered Cardiovascular TissuesR33HL089027 · NHLBI · STANFORD UNIVERSITY · PI WU, JOSEPH C. · 2009 to 2011
$2.3M
Molecular and Cellular Phenotype of Aging and iPS CellsRC1AG036142 · NIA · STANFORD UNIVERSITY · PI WEINBERG, KENNETH I, WU, JOSEPH C. · 2010 to 2010
$1000k
Molecular Imaging of Resident Cardiac Stem CellsRC1HL099117 · NHLBI · STANFORD UNIVERSITY · PI WU, JOSEPH C. · 2009 to 2010
$1000k
NHLBI NIH HHS R01 HL061535NHLBI NIH HHS R33 HL089027NHLBI NIH HHS RC1 HL099117NIA NIH HHS RC1 AG036142NIA NIH HHS RC1AG036142NIBIB NIH HHS R01 EB006745NIH HHS DP2 OD004437NIH HHS DP2OD004437
6 · The paper itself

Abstract

Immature primary and stem cell-derived cardiomyocytes provide useful models for fundamental studies of heart development and cardiac disease, and offer potential for patient specific drug testing and differentiation protocols aimed at cardiac grafts. To assess their potential for augmenting heart function, and to gain insight into cardiac growth and disease, tissue engineers must quantify the contractile forces of these single cells. Currently, axial contractile forces of isolated adult heart cells can only be measured by two-point methods such as carbon fiber techniques, which cannot be applied to neonatal and stem cell-derived heart cells because they are more difficult to handle and lack a persistent shape. Here we present a novel axial technique for measuring the contractile forces of isolated immature cardiomyocytes. We overcome cell manipulation and patterning challenges by using a thermoresponsive sacrificial support layer in conjunction with arrays of widely separated elastomeric microposts. Our approach has the potential to be high-throughput, is functionally analogous to current gold-standard axial force assays for adult heart cells, and prescribes elongated cell shapes without protein patterning. Finally, we calibrate these force posts with piezoresistive cantilevers to dramatically reduce measurement error typical for soft polymer-based force assays. We report quantitative measurements of peak contractile forces up to 146 nN with post stiffness standard error (26 nN) far better than that based on geometry and stiffness estimates alone. The addition of sacrificial layers to future 2D and 3D cell culture platforms will enable improved cell placement and the complex suspension of cells across 3D constructs.

Indexed as

Mechanical PhenomenaAnimalsAnimals, NewbornBiomechanical PhenomenaCell ShapeEmbryonic Stem CellsHumansMyocytes, CardiacRatsTissue Array Analysis

Identifiers

PMID23007494
PMCPMC3545035
OpenAlexW2020203296

What OpenQuestion holds

Textmetadata
LicenceTDM
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.