Evidence map›Paper›PMID 34832798›Full record

ArticleMicromachines2021

Wafer-Scale Patterning of Protein Templates for Hydrogel Fabrication.

Anna A Kim, Erica A Castillo, Kerry V Lane, Gabriela V Torres, Orlando Chirikian, Robin E Wilson, Sydney A Lance, Gaspard Pardon, Beth L Pruitt

Abstract read
In one paragraph

Article in Micromachines, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

9 authors.

Anna A KimDepartment of Materials Science and Engineering, Uppsala University, 751 03 Uppsala, Sweden.ORCID 0000-0003-1861-3801
Erica A CastilloDepartment of Mechanical Engineering, University of California, Santa Barbara, CA 93106, USA.
Kerry V LaneDepartment of Mechanical Engineering, University of California, Santa Barbara, CA 93106, USA.ORCID 0000-0003-3099-9217
Gabriela V TorresDepartment of Mechanical Engineering, University of California, Santa Barbara, CA 93106, USA.
Orlando ChirikianBiomolecular Science and Engineering Program, University of California, Santa Barbara, CA 93106, USA.
Robin E WilsonDepartment of Mechanical Engineering, Stanford University, Stanford, CA 94305, USA.
Sydney A LanceDepartment of Mechanical Engineering, Stanford University, Stanford, CA 94305, USA.
Gaspard PardonDepartment of Bioengineering, School of Engineering and School of Medicine, Stanford University, Stanford, CA 94305, USA.ORCID 0000-0001-9177-1174
Beth L PruittDepartment of Mechanical Engineering, University of California, Santa Barbara, CA 93106, USA.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
Effect of Microgravity on Drug Responses Using Engineered Heart TissuesUH3TR002588 · NCATS · STANFORD UNIVERSITY · PI PRUITT, BETH L, WU, JOSEPH C. · 2020 to 2022
$1.6M
National Science Foundation CMMI 1834760NCATS NIH HHS UH3 TR002588NIGMS NIH HHS RM1 GM131981NIH HHS 4UH3TR002588-03NIH HHS 5RM1GM131981-02Swedish Research Council 2017-06156
6 · The paper itself

Abstract

Human-induced pluripotent stem cell-derived cardiomyocytes are a potentially unlimited cell source and promising patient-specific in vitro model of cardiac diseases. Yet, these cells are limited by immaturity and population heterogeneity. Current in vitro studies aiming at better understanding of the mechanical and chemical cues in the microenvironment that drive cellular maturation involve deformable materials and precise manipulation of the microenvironment with, for example, micropatterns. Such microenvironment manipulation most often involves microfabrication protocols which are time-consuming, require cleanroom facilities and photolithography expertise. Here, we present a method to increase the scale of the fabrication pipeline, thereby enabling large-batch generation of shelf-stable microenvironment protein templates on glass chips. This decreases fabrication time and allows for more flexibility in the subsequent steps, for example, in tuning the material properties and the selection of extracellular matrix or cell proteins. Further, the fabrication of deformable hydrogels has been optimized for compatibility with these templates, in addition to the templates being able to be used to acquire protein patterns directly on the glass chips. With our approach, we have successfully controlled the shapes of cardiomyocytes seeded on Matrigel-patterned hydrogels.

Indexed as

hydrogelslift-off protein patterningmicrofabricationsingle-cell analysissingle-cell cardiomyocytes

Identifiers

PMID34832798
PMCPMC8620583

What OpenQuestion holds

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LicenceCC BY
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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.