Evidence map›Paper›PMID 35595094›Full record

ArticleExperimental eye research2022

ECM stiffness modulates the proliferation but not the motility of primary corneal keratocytes in response to PDGF-BB.

Krithika S Iyer, Daniel P Maruri, Kara E Peak, David W Schmidtke, W Matthew Petroll, Victor D Varner

Open access · greenAbstract read
In one paragraph

Article in Experimental eye research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

10 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
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  3. Article
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  9. Review
  10. Unraveling the mechanobiology of cornea: From bench side to the clinic.Frontiers in bioengineering and biotechnology · 2022
    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

6 authors at 2 institutions in 1 country.

Krithika S IyerDepartment of Bioengineering, University of Texas at Dallas, Richardson, TX, USA.
Daniel P MaruriDepartment of Bioengineering, University of Texas at Dallas, Richardson, TX, USA.
Kara E PeakDepartment of Bioengineering, University of Texas at Dallas, Richardson, TX, USA.
David W SchmidtkeDepartment of Bioengineering, University of Texas at Dallas, Richardson, TX, USA; Department of Surgery, UT Southwestern Medical Center, Dallas, TX, USA.
W Matthew PetrollDepartment of Ophthalmology, UT Southwestern Medical Center, Dallas, TX, USA.
Victor D VarnerDepartment of Bioengineering, University of Texas at Dallas, Richardson, TX, USA; Department of Surgery, UT Southwestern Medical Center, Dallas, TX, USA. Electronic address: vdv@utdallas.edu.
The University of Texas at Dallas · USSouthwestern Medical Center · US

Funding

Stem Cell, Organoid and Cell Phenotyping ModuleP30EY030413 · NEI · UT SOUTHWESTERN MEDICAL CENTER · PI W MATTHEW PETROLL · 2019 to 2026
$5.9M
Regulation of Corneal Keratocyte Differentiation through the Integration of Biochemical, Biomechanical and Topographic CuesR01EY030190 · NEI · UNIVERSITY OF TEXAS DALLAS · PI SCHMIDTKE, DAVID W · 2019 to 2024
$1.9M
NEI NIH HHS P30 EY030413NEI NIH HHS R01 EY030190
6 · The paper itself

Abstract

During corneal wound healing, keratocytes present within the corneal stroma become activated into a repair phenotype upon the release of growth factors, such as transforming growth factor-beta 1 (TGF-β1) and platelet-derived growth factor-BB (PDGF-BB). The process of injury and repair can lead to changes in the mechanical properties of the tissue, and previous work has shown that the TGF-β1-mediated myofibroblast differentiation of corneal keratocytes depends on substratum stiffness. It is still unclear, however, if changes in stiffness can modulate keratocyte behavior in response to other growth factors, such as PDGF-BB. Here, we used a polyacrylamide (PA) gel system to determine whether changes in stiffness influence the proliferation and motility of primary corneal keratocytes treated with PDGF-BB. In the presence of PDGF-BB, cells on stiffer substrata exhibited a more elongated morphology and had higher rates of proliferation than cells in a more compliant microenvironment. Using a freeze-injury to assay cell motility, however, we did not observe any stiffness-dependent differences in the migration of keratocytes treated with PDGF-BB. Taken together, these data highlight the importance of biophysical cues during corneal wound healing and suggest that keratocytes respond differently to changes in ECM stiffness in the presence of different growth factors.

Indexed as

Corneal KeratocytesTransforming Growth Factor beta1BecaplerminCell MovementCell ProliferationCells, CulturedPlatelet-Derived Growth FactorBecaplerminPlatelet-Derived Growth FactorTransforming Growth Factor beta1BiomechanicsCorneal wound healingFreeze injuryMechanobiologyPlatelet-derived growth factor

Identifiers

PMID35595094
PMCPMC10163834
OpenAlexW4280571770

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.