Evidence map›Paper›PMID 37103307›Full record

ArticleJournal of functional biomaterials2023

Effects of Topography and PDGF on the Response of Corneal Keratocytes to Fibronectin-Coated Surfaces.

Kevin H Lam, Tarik Z Shihabeddin, Jacob A Awkal, Alex M Najjar, Miguel Miron-Mendoza, Daniel P Maruri, Victor D Varner, W Matthew Petroll, David W Schmidtke

Abstract read
In one paragraph

Article in Journal of functional biomaterials, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Squishy matters - Corneal mechanobiology in health and disease.Progress in retinal and eye research · 2024
    Review
  7. Fabrication of Micropatterns of Aligned Collagen Fibrils.Langmuir : the ACS journal of surfaces and colloids · 2024
    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.

Kevin H LamDepartment of Bioengineering, University of Texas at Dallas, Richardson, TX 75080, USA.
Tarik Z ShihabeddinDepartment of Bioengineering, University of Texas at Dallas, Richardson, TX 75080, USA.
Jacob A AwkalDepartment of Bioengineering, University of Texas at Dallas, Richardson, TX 75080, USA.ORCID 0000-0001-9472-3346
Alex M NajjarDepartment of Bioengineering, University of Texas at Dallas, Richardson, TX 75080, USA.ORCID 0000-0003-0827-8456
Miguel Miron-MendozaDepartment of Ophthalmology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Daniel P MaruriDepartment of Bioengineering, University of Texas at Dallas, Richardson, TX 75080, USA.
Victor D VarnerDepartment of Bioengineering, University of Texas at Dallas, Richardson, TX 75080, USA.
W Matthew PetrollDepartment of Ophthalmology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.ORCID 0000-0003-0795-4539
David W SchmidtkeDepartment of Bioengineering, University of Texas at Dallas, Richardson, TX 75080, USA.ORCID 0000-0001-6404-318X

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 EY030190NIH HHS P30 EY030413NIH HHS R01 EY030190
6 · The paper itself

Abstract

During corneal wound healing, corneal keratocytes are exposed to both biophysical and soluble cues that cause them to transform from a quiescent state to a repair phenotype. How keratocytes integrate these multiple cues simultaneously is not well understood. To investigate this process, primary rabbit corneal keratocytes were cultured on substrates patterned with aligned collagen fibrils and coated with adsorbed fibronectin. After 2 or 5 days of culture, keratocytes were fixed and stained to assess changes in cell morphology and markers of myofibroblastic activation by fluorescence microscopy. Initially, adsorbed fibronectin had an activating effect on the keratocytes as evidenced by changes in cell shape, stress fiber formation, and expression of alpha-smooth muscle actin (α-SMA). The magnitude of these effects depended upon substrate topography (i.e., flat substrate vs aligned collagen fibrils) and decreased with culture time. When keratocytes were simultaneously exposed to adsorbed fibronectin and soluble platelet-derived growth factor-BB (PDGF-BB), the cells elongated and had reduced expression of stress fibers and α-SMA. In the presence of PDGF-BB, keratocytes plated on the aligned collagen fibrils elongated in the direction of the fibrils. These results provide new information on how keratocytes respond to multiple simultaneous cues and how the anisotropic topography of aligned collagen fibrils influences keratocyte behavior.

Indexed as

collagen fibrilscorneal keratocytesfibronectinmicrofluidicsplatelet-derived growth factortopographywound healing

Identifiers

PMID37103307
PMCPMC10144166

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Registered trials

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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.