Evidence map›Paper›PMID 25236849›Full record

ArticleScientific reports2014

Mechanosensitive kinases regulate stiffness-induced cardiomyocyte maturation.

Jennifer L Young, Kyle Kretchmer, Matthew G Ondeck, Alexander C Zambon, Adam J Engler

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.6field-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

36 citing papers in PubMed, 70 citations in OpenAlex.

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  7. The Utilisation of Hydrogels for iPSC-Cardiomyocyte Research.International journal of molecular sciences · 2023
    Review
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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

5 authors at 1 institution in 1 country.

Jennifer L YoungDepartment of Bioengineering, University of California, San Diego, CA 92093.
Kyle KretchmerDepartment of Bioengineering, University of California, San Diego, CA 92093.
Matthew G OndeckDepartment of Material Science Program, University of California, San Diego, CA 92093.
Alexander C ZambonDepartment of Pharmacology, University of California, San Diego, CA 92093.
Adam J Engler1] Department of Bioengineering, University of California, San Diego, CA 92093 [2] Department of Material Science Program, University of California, San Diego, CA 92093 [3] Sanford Consortium for Regenerative Medicine, La Jolla, CA 92037.
University of California, San Diego · US

Funding

Stem Cells and Dynamic Materials Improve Cardiac Function Post-mycardial InfarctiR21HL106529 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ENGLER, ADAM J · 2011 to 2012
$426k
NHLBI NIH HHS R21 HL106529NHLBI NIH HHS R21HL106529PHITPO CDC HHS 1U54HK08460 A
6 · The paper itself

Abstract

Cells secrete and assemble extracellular matrix throughout development, giving rise to time-dependent, tissue-specific stiffness. Mimicking myocardial matrix stiffening, i.e. ~10-fold increase over 1 week, with a hydrogel system enhances myofibrillar organization of embryonic cardiomyocytes compared to static hydrogels, and thus we sought to identify specific mechanosensitive proteins involved. Expression and/or phosphorylation state of 309 unique protein kinases were examined in embryonic cardiomyocytes plated on either dynamically stiffening or static mature myocardial stiffness hydrogels. Gene ontology analysis of these kinases identified cardiogenic pathways that exhibited time-dependent up-regulation on dynamic versus static matrices, including PI3K/AKT and p38 MAPK, while GSK3β, a known antagonist of cardiomyocyte maturation, was down-regulated. Additionally, inhibiting GSK3β on static matrices improved spontaneous contraction and myofibril organization, while inhibiting agonist AKT on dynamic matrices reduced myofibril organization and spontaneous contraction, confirming its role in mechanically-driven maturation. Together, these data indicate that mechanically-driven maturation is at least partially achieved via active mechanosensing at focal adhesions, affecting expression and phosphorylation of a variety of protein kinases important to cardiomyogenesis.

Indexed as

AnimalsCell CommunicationChick EmbryoGene Expression RegulationMAP Kinase Signaling SystemMyocytes, CardiacPhosphorylationProtein KinasesProto-Oncogene Proteins c-aktSignal TransductionTissue Array AnalysisVascular StiffnessProtein KinasesProto-Oncogene Proteins c-akt

Identifiers

PMID25236849
PMCPMC4168277
OpenAlexW2010081173

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.