Evidence map›Paper›PMID 24582552›Full record

ArticleBiomaterials2014

Micropattern width dependent sarcomere development in human ESC-derived cardiomyocytes.

Max R Salick, Brett N Napiwocki, Jin Sha, Gavin T Knight, Shahzad A Chindhy, Timothy J Kamp, Randolph S Ashton, Wendy C Crone

Open access · greenAbstract read
In one paragraph

Article in Biomaterials, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed, 2 pooled it
9.4field-weighted citation impact, top 1% 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

73 citing papers in PubMed, 2 syntheses or guidelines pooled it, 158 citations in OpenAlex.

  1. Engineering the maturation of stem cell-derived cardiomyocytes.Frontiers in bioengineering and biotechnology · 2023
    Pooled it
  2. Pooled it
  3. Article
  4. Review
  5. Living Nanofiber-Enabled Cardiac Patches for Myocardial Injury.JACC. Basic to translational science · 2025
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Fabrication of Micropatterns of Aligned Collagen Fibrils.Langmuir : the ACS journal of surfaces and colloids · 2024
    Article
  12. Review
  13. Advances in Regulating Cellular Behavior Using Micropatterns.The Yale journal of biology and medicine · 2023
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article

13 more citing papers are in PubMed but not listed here.

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

8 authors at 2 institutions in 2 countries.

Max R SalickWisconsin Institutes for Discovery, 330 N Orchard St, Madison, WI 53715, USA; Department of Engineering Physics, University of Wisconsin - Madison, 1500 Engineering Drive, Madison, WI 53706, USA; Materials Science Program, University of Wisconsin - Madison, 1509 University Ave, Madison, WI 53706, USA.
Brett N NapiwockiWisconsin Institutes for Discovery, 330 N Orchard St, Madison, WI 53715, USA; Department of Biomedical Engineering, University of Wisconsin - Madison, 1550 Engineering Drive, Madison, WI 53706, USA.
Jin ShaWisconsin Institutes for Discovery, 330 N Orchard St, Madison, WI 53715, USA; School of Mechanical and Power Engineering, East China University of Science and Technology, Shanghai, China.
Gavin T KnightWisconsin Institutes for Discovery, 330 N Orchard St, Madison, WI 53715, USA; Department of Biomedical Engineering, University of Wisconsin - Madison, 1550 Engineering Drive, Madison, WI 53706, USA.
Shahzad A ChindhyDepartment of Medicine, School of Medicine and Public Health, University of Wisconsin - Madison, 750 Highland Ave, Madison, WI 53706, USA.
Timothy J KampWisconsin Institutes for Discovery, 330 N Orchard St, Madison, WI 53715, USA; Department of Medicine, School of Medicine and Public Health, University of Wisconsin - Madison, 750 Highland Ave, Madison, WI 53706, USA; WiCell Institute, 614 Walnut Street, Madison, WI 53726, USA; Department of Cell and Regenerative Biology, School of Medicine and Public Health, University of Wisconsin - Madison, 1300 University Ave, Madison, WI 53706, USA.
Randolph S AshtonWisconsin Institutes for Discovery, 330 N Orchard St, Madison, WI 53715, USA; Department of Biomedical Engineering, University of Wisconsin - Madison, 1550 Engineering Drive, Madison, WI 53706, USA.
Wendy C CroneWisconsin Institutes for Discovery, 330 N Orchard St, Madison, WI 53715, USA; Department of Engineering Physics, University of Wisconsin - Madison, 1500 Engineering Drive, Madison, WI 53706, USA; Materials Science Program, University of Wisconsin - Madison, 1509 University Ave, Madison, WI 53706, USA; Department of Biomedical Engineering, University of Wisconsin - Madison, 1550 Engineering Drive, Madison, WI 53706, USA. Electronic address: crone@engr.wisc.edu.
University of Wisconsin–Madison · USWisconsin Institutes for Discovery · US

Funding

Midwest Progenitor Cell ConsortiumU01HL099773 · NHLBI · UNIVERSITY OF WISCONSIN-MADISON · PI THOMSON, JAMES ALEXANDER · 2009 to 2015
$7.8M
Mechanical Control of Stem Cell DifferentiationK18HL105504 · NHLBI · UNIVERSITY OF WISCONSIN-MADISON · PI CRONE, WENDY CATHERINE · 2011 to 2012
$328k
NHLBI NIH HHS K18 HL105504NHLBI NIH HHS U01 HL099773
6 · The paper itself

Abstract

In this study, human embryonic stem cell-derived cardiomyocytes were seeded onto controlled two-dimensional micropatterned features, and an improvement in sarcomere formation and cell alignment was observed in specific feature geometries. High-resolution photolithography techniques and microcontact printing were utilized to produce features of various rectangular geometries, with areas ranging from 2500 μm(2) to 160,000 μm(2). The microcontact printing method was used to pattern non-adherent poly(ethylene glycol) regions on gold coated glass slides. Matrigel and fibronectin extracellular matrix (ECM) proteins were layered onto the gold-coated glass slides, providing a controlled geometry for cell adhesion. We used small molecule-based differentiation and an antibiotic purification step to produce a pure population of immature cardiomyocytes from H9 human embryonic stem cells (hESCs). We then seeded this pure population of human cardiomyocytes onto the micropatterned features of various sizes and observed how the cardiomyocytes remodeled their myofilament structure in response to the feature geometries. Immunofluorescence was used to measure α-actinin expression, and phalloidin stains were used to detect actin presence in the patterned cells. Analysis of nuclear alignment was also used to determine how cell direction was influenced by the features. The seeded cells showed clear alignment with the features, dependent on the width rather than the overall aspect ratio of the features. It was determined that features with widths between 30 μm and 80 μm promoted highly aligned cardiomyocytes with a dramatic increase in sarcomere alignment relative to the long axis of the pattern. This creation of highly-aligned cell aggregates with robust sarcomere structures holds great potential in advancing cell-based pharmacological studies, and will help researchers to understand the means by which ECM geometries can affect myofilament structure and maturation in hESC-derived cardiomyocytes.

Indexed as

Cell AdhesionCell DifferentiationCell LineCollagenDrug CombinationsEmbryonic Stem CellsFibronectinsGoldHumansLamininMyocytes, CardiacProteoglycansSarcomeresSurface PropertiesTissue EngineeringTissue ScaffoldsCollagenDrug CombinationsFibronectinsGoldLamininmatrigelProteoglycansCardiac tissue engineeringCardiomyocyteCell morphologyMicropatterningStem cellSurface modification

Identifiers

PMID24582552
PMCPMC4026015
OpenAlexW2124033487

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.