Evidence map›Paper›PMID 24459068›Full record

ArticleAdvanced healthcare materials2014

Clickable, photodegradable hydrogels to dynamically modulate valvular interstitial cell phenotype.

Chelsea M Kirschner, Daniel L Alge, Sarah T Gould, Kristi S Anseth

Abstract read
In one paragraph

Article in Advanced healthcare materials, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

35 citing papers in PubMed, 62 citations in OpenAlex.

  1. Review
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  10. Engineered microenvironment for the study of myofibroblast mechanobiology.Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society · 2021
    Article
  11. Review
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  15. Review
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  17. Embedding of Precision-Cut Lung Slices in Engineered Hydrogel Biomaterials Supports ExtendedAmerican journal of respiratory cell and molecular biology · 2020
    Article
  18. Article
  19. Article
  20. Tissue-informed engineering strategies for modeling human pulmonary diseases.American journal of physiology. Lung cellular and molecular physiology · 2019
    Review
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

4 authors at 2 institutions in 1 country.

Chelsea M KirschnerDepartment of Chemical and Biological Engineering and the BioFrontiers Institute, University of Colorado, 596 UCB, Boulder, CO, 80303-0596, USA.
Daniel L Alge
Sarah T Gould
Kristi S Anseth
University of Colorado Boulder · USHoward Hughes Medical Institute · US

Funding

Bioactive Hydrogel Niches for 3D VIC CultureR01HL089260 · NHLBI · UNIVERSITY OF COLORADO · PI ANSETH, KRISTI S. · 2008 to 2011
$1.3M
Hydrogel Scaffolds with Engineered Dynamically Tunable Topographies for hMSC DiffF32AR061923 · NIAMS · UNIVERSITY OF COLORADO · PI MAGIN, CHELSEA M · 2011 to 2012
$99k
Howard Hughes Medical InstituteNHLBI NIH HHS R01 HL089260NIAMS NIH HHS F32 AR061923NIAMS NIH HHS F32AR061923
6 · The paper itself

Abstract

Biophysical cues are widely recognized to influence cell phenotype. While this evidence was established using static substrates, there is growing interest in creating stimulus-responsive biomaterials that better recapitulate the dynamic extracellular matrix. Here, a clickable, photodegradable hydrogel substrate that allows the user to precisely control substrate elasticity and topography in situ is presented. The hydrogels are synthesized by reacting an 8-arm poly(ethylene glycol) alkyne with an azide-functionalized photodegradable crosslinker. The utility of this platform by exploiting its photoresponsive properties to modulate the phenotype of porcine aortic valvular interstitial cells (VICs) is demonstrated. First, VIC phenotype is monitored, in response to initial substratum modulus and static topographic cues. Higher modulus (E ≈ 15 kPa) substrates induce higher levels of activation (≈70% myofibroblasts) versus soft (E ≈ 3 kPa) substrates (≈20% myofibroblasts). Microtopographies that induce VIC alignment and elongation on low modulus substrates also stimulate activation. Finally, VIC phenotype is monitored in response to sequential in situ manipulations. The results illustrate that VIC activation on stiff surfaces (≈70% myofibroblasts) can be partially reversed by reducing surface modulus (≈30% myofibroblats) and subsequently re-activated by anisotropic topographies (≈60% myofibroblasts). Such dynamic substrates afford unique opportunities to decipher the complex role of matrix cues on the plasticity of VIC activation.

Indexed as

AnimalsAortic ValveCell Culture TechniquesCells, CulturedElastic ModulusHydrogelsPhenotypePhotolysisSwineTissue ScaffoldsHydrogelshydrogelsmicrotopographiesmyofibroblastsphotoresponsive material propertiesvalvular interstitial cells

Identifiers

PMID24459068
PMCPMC11949079
OpenAlexW2053953238

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.